Here we collect a list of links to interesting and valued science papers and press articles as our reference to the research on medicine and specially oncology.
We recommend to check these information blog on all Cannabinioid research related topics: http://www.thctotalhealthcare.com
An article about the Ben Williams case:
https://www.telegraph.co.uk/lifestyle/wellbeing/healthadvice/11424747/The-professor-who-cured-his-cancer-with-a-cocktail-of-everyday-pills-and-20-years-on-remains-disease-free.html
His regime: https://virtualtrials.com/pdf2017/treatment_options_gbm_2017.pdf
Celecoxib: a potent mitochondrial pro-oxidant cytotoxic agent sensitizing metastatic cancers and cancer stem cells to chemotherapy
https://doi.org/10.20517/2394-4722.2018.42
Treatment of hepatocarcinoma with Celecoxib and Pentoxifylline
https://www.medigraphic.com/pdfs/imss/im-2018/im183o.pdf
Chloroquine activates the p53 pathway and induces apoptosis in human glioma cells
https://doi.org/10.1093/neuonc/nop046
Oridonin inhibits metastasis of human ovarian cancer cells by suppressing the mTOR pathway
https://doi.org/10.5114/aoms.2018.77068
Simvastatin in combination with bergamottin potentiates TNF induced apoptosis through modulation of NF B signalling pathway in human CML
https://doi.org/10.3109/13880209.2016.1141221
Combination simvastatin and metformin synergistically inhibits endometrial cancer cell growth
https://doi.org/10.1016/j.ygyno.2019.05.022
Niclosamide induces mitochondria fragmentation and promotes both apoptotic and autophagic cell death
http://dx.doi.org/10.5483/BMBRep.2011.44.8.517
Nitazoxanide – small molecule promotes b-catenin citrullination and inhibits Wnt signaling in cancer
http://dx.doi.org/10.1038/nchembio.2510
NICLOSAMIDE FOR THE TREATMENT OF CANCER METASTASES
US patent: US20140294957A1
https://patents.google.com/patent/US20140294957A1/en
NICLOSAMIDE AND ITS DERIVATIVES FOR USE IN THE TREATMENT OF SOLID TUMORS
US patent: US9844522B2
https://patents.google.com/patent/US9844522B2/ja
Niclosamide inhibits lytic replication of Epstein-Barr virus by disrupting mTOR activation
http://dx.doi.org/10.1016/j.antiviral.2016.12.002
Drug Repurposing of the Anthelmintic Niclosamide to Treat Multidrug-Resistant Leukemia
https://doi.org/10.3389/fphar.2017.00110
Multi-targeted therapy of cancer by Niclosamide: A new application for an old drug
http://dx.doi.org/10.1016/j.canlet.2014.04.003
Niclosamide: Beyond an antihelminthic drug
http://dx.doi.org/10.1016/j.cellsig.2017.04.001
Niclosamide inhibits the proliferation of human osteosarcoma cell lines by inducing apoptosis and cell cycle arrest
https://www.spandidos-publications.com/or/33/4/1763
Niclosamide repositioning for treating cancer: Challenges and nano-based drug delivery opportunities
https://doi.org/10.1016/j.ejpb.2019.05.004
Drug repurposing to overcome resistance to various therapies for colorectal cancer
https://doi.org/10.1007/s00018-019-03134-0
The Use of Endogenous and Synthetic Cannabinoids in Prostate Cancer Therapy – Thesis
https://tspace.library.utoronto.ca/handle/1807/91450
Targeting the endocannabinoid system in cancer therapy: A call for further research
The Effects of Cannabidiol and – Tetrahydrocannabinol Concentration on Breast Cancer Cell Viability
https://www.embopress.org/lookup/doi/10.15252/emmm.201809034
Cannabinoid pharmacology and therapy in gut disorders
https://doi.org/10.1016/j.bcp.2018.07.048
Towards natural mimetics of metformin and rapamycin
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723685/
The CB 2 cannabinoid receptor signals apoptosis via ceramide-dependent activation of the mitochondrial intrinsic pathway
http://dx.doi.org/10.1016/j.yexcr.2006.03.009
Retinoic Acid Receptor b Mediates the Growth-Inhibitory Effect of Retinoic Acid by Promoting Apoptosis in Human Breast Cancer Cells
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC231096/
Melatonin Can Strengthen the Effect of Retinoic Acid in HL-60 Cells
http://dx.doi.org/10.3390/ijms19102873
The success and the challenge of all-trans retinoic acid in the treatment of cancer
https://doi.org/10.1080/10408398.2018.1509201
Therapeutic Targeting of Autophagy
http://dx.doi.org/10.1016/j.ebiom.2016.10.034
Therapeutic strategies of drug repositioning targeting autophagy to induce cancer cell death: from pathophysiology to treatment
https://www.ncbi.nlm.nih.gov/pubmed/28279189
Cannabidiol enhances anandamide signaling and alleviates psychotic symptoms of schizophrenia
http://dx.doi.org/10.1038/tp.2012.15
Wild-Type p53 Promotes Cancer Metabolic Switch by Inducing PUMA-Dependent Suppression of Oxidative Phosphorylation
https://doi.org/10.1016/j.ccell.2018.12.012
Synthetic Cannabinoid Activity Against Colorectal Cancer Cells
https://doi.org/10.1089/can.2018.0065
Disulfiram reduces metastatic osteosarcoma tumor burden in an immunocompetent Balb/c or-thotopic mouse model
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6059028/
Anti-cancer effects of disulfiram in head and neck squamous cell carcinoma via autophagic cell death
https://doi.org/10.1371/journal.pone.0203069
Dietary ω-3 Polyunsaturated Fatty Acids Inhibit Tumor Growth in Transgenic Apc Min Mice, Correlating with CB1 Receptor Up-Regulation
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372501/
Chloroquine-Inducible Par-4 Secretion Is Essential for Tumor Cell Apoptos is and Inhibition of Metastasis
http://dx.doi.org/10.1016/j.celrep.2016.12.051
Anticancer Activity and Mechanism of Xanthohumol – A Prenylated Flavonoid From Hops
https://doi.org/10.3389/fphar.2018.00530
Time to use a dose of Chloroquine as an adjuvant to anti-cancer chemotherapies
http://dx.doi.org/10.1016/j.ejphar.2015.12.017
The Utility of Chloroquine in Cancer Therapy
https://www.ncbi.nlm.nih.gov/pubmed/25734693
NF-kB activation induced by chloroquine requires autophagosome p62, and JNK signaling and promotes tumor cell resistance
http://www.jbc.org/cgi/doi/10.1074/jbc.M116.756536
Inhibition of autophagy with chloroquine is effective in melanoma
http://dx.doi.org/10.1016/j.jss.2013.04.055
Ferroquine, the next generation antimalarial drug, has antitumor activity
https://www.nature.com/articles/s41598-017-16154-2
Targeting ALDH1A1 by disulfiram/copper complex inhibits non-small cell lung cancer recurrence driven by ALDH-positive cancer stem cells
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295448/
Inhibitory effect of Disulfiram copper complex on non-small cell lung cancer cells
http://dx.doi.org/10.1016/j.bbrc.2014.03.047
Chloroquine Promotes Apoptosis in Melanoma Cells by Inhibiting BH3 Domain–Mediated PUMA Degradation
http://dx.doi.org/10.1038/jid.2013.56
Chloroquine inhibits cell growth and induces cell death in A549 lung cancer cells
http://europepmc.org/abstract/med/16413786
Chloroquine Eliminates Cancer Stem Cells Through Deregulation of Jak2 and DNMT1
http://dx.doi.org/10.1002/stem.1746
Chloroquine and hydroxychloroquine as anti-cancer agents
https://doi.org/10.3332/ecancer.2017.781
Chloroquine and its analogs: A new promise of an old drug for effective and safe cancer therapies
http://dx.doi.org/10.1016/j.ejphar.2009.06.063
Suppressing autophagy enhances disulfiram/copper-induced apoptosis in non-small cell lung cancer
https://doi.org/10.1016/j.ejphar.2018.02.039
Autophagy Modulation in Cancer – Current Knowledge on Action and Therapy
https://doi.org/10.1155/2018/8023821
Anticancer and antimetastatic effects of cordycepin, an active component of Cordyceps sinensis
http://dx.doi.org/10.1016/j.jphs.2014.09.001
Cordycepin induces apoptotic cell death of human brain cancer through the modulation of autophagy
http://dx.doi.org/10.1016/j.tiv.2017.10.002
Oridonin inhibits BxPC-3 cell growth through cell apoptosis
https://doi.org/10.1093/abbs/gmu134
Disulfiram inhibits activating transcription factor cyclic AMP-responsive element binding protein and human melanoma growth in a metal-dependent manner in vitro, in mice and in a patient with metastatic disease

and positron emission spectrographs (bottom) of a 64-year-old woman with stage IV ocular melanoma metastatic to the liver. Before treatment, she had a
5.5 cm central liver metastasis (white arrows). After 3 months of treatment with disulfiram (500 mg/d) and zinc gluconate (50 mg thrice daily), the hepatic
metastasis had decreased in volume by >50% in both scans (white arrows). After continuing treatment with disulfiram (250 mg/d) and the same dose of
zinc gluconate, the lesion remained stable in size at 10 and 14 months (white arrows). She continues to be clinically well and free of drug side effects on
disulfiram and zinc gluconate. After 53 continuous months of treatment with this regimen, she has experienced no quantifiable malignant progression. A
follow-up abdominal computed tomography scan after 42 months of therapy shows that the hepatic tumor burden has remained small.
See also U.S. patents No. 6,548,540 and 6,589,987
http://mct.aacrjournals.org/content/3/9/1049.long
The cytotoxic mechanisms of disulfiram and copper in cancer cells
https://pubs.rsc.org/en/content/articlelanding/2015/tx/c5tx00210a
CANNABIDIOL (CBD) Pre-Review Report Expert Committee 5.2 WHO
Under experimental conditions,it has been demonstrated that heating CBD in solutions of some acidscatalysescyclizations within the CBDmolecule resulting in delta-9-THC[28]. Gaoni and Mechoulam have published several papers regarding methods of converting CBD to other cannabinoids including THC, however the yields vary and purity is unclear. [9]A version of thismethod has been reported on a drug user forum. Itsuggests dissolving CBD in sulphuric acid/acetic acid and leaving it for anywhere from3 hours to 3 days to obtain delta-9-THC and delta-8-THC. After 3 hours, the author states that CBD has been converted into 52% delta-9-THC and 2% delta-8-THC.
https://www.who.int/medicines/access/controlled-substances/5.2_CBD.pdf
Cannabis Extract Treatment for Terminal Acute Lymphoblastic Leukemia with a Philadelphia Chromosome Mutation
https://www.karger.com/Article/FullText/356446
Future Aspects for Cannabinoids in Breast Cancer Therapy
http://dx.doi.org/10.3390/ijms20071673
The Endocannabinoid System as a Target in Cancer Diseases
https://doi.org/10.3389/fphar.2019.00339
Antitumor Cannabinoid Chemotypes – Structural Insights
https://doi.org/10.3389/fphar.2019.00621
CANNABINOIDS INCREASE LUNG CANCER CELL LYSIS BY LYMPHOKINE-ACTIVATED KILLER CELLS VIA UPREGULATION OF ICAM-1
http://dx.doi.org/doi:10.1016/j.bcp.2014.07.014
Novel mechanism of cannabidiol-induced apoptosis in breast cancer cell lines
https://doi.org/10.1016/j.breast.2018.06.009
Cannabidiol-induced apoptosis is mediated by activation of Noxa in human colorectal cancer cells
https://doi.org/10.1016/j.canlet.2019.01.011
Cannabidiol Enhances the Therapeutic Effects of TRAIL by Upregulating DR5 in Colorectal Cancer
http://dx.doi.org/10.3390/cancers11050642
Silibinin to improve cancer therapeutics, as an apoptotic inducer, autophagy modulator, cell cycle inhibitor, and microRNAs regulator
https://doi.org/10.1016/j.lfs.2018.10.009
Melanoma Cell Death Mechanisms
https://doi.org/10.4068/cmj.2018.54.3.135
Natural Forms of Vitamin E and Metabolites Regulation of Cancer Cell Death and Underlying Mechanisms
https://doi.org/10.1002/iub.1978
Curcumin and Solid Lipid Curcumin Particles Induce Autophagy, but Inhibit Mitophagy and the PI3K-Akt/mTOR Pathway in Cultured Glioblastoma Cells
http://dx.doi.org/10.3390/ijms20020399
Silibinin, A Natural Blend In Polytherapy Formulation For Targeting CD44V6 Expressing Colon Cancer Stem Cells
https://www.nature.com/articles/s41598-018-35069-0
Targeting Autophagy Using Natural Compounds for Cancer Prevention and Therapy
https://onlinelibrary.wiley.com/doi/abs/10.1002/cncr.31978
Inhibitory Effect of CAPE and Kaempferol in Colon Cancer Cell Lines – Possible Implications in New Therapeutic Strategies
http://dx.doi.org/10.3390/ijms20051199
p53 Signaling in Cancers
http://dx.doi.org/10.3390/cancers11030332
Resveratrol inhibited the progression of human hepatocellular carcinoma by inducing autophagy via regulating p53 and the phosphoinositide 3‑kinase protein kinase B pathway
https://doi.org/10.3892/or.2018.6648
Role of Autophagy in Apoptotic Regulation by Akt in Pancreatic Cancer
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4565513
Autophagy sustains the survival of human pancreatic cancer PANC-1 cells under extreme nutrient deprivation conditions
http://dx.doi.org/10.1016/j.bbrc.2015.05.022
Doxycycline, Azithromycin and Vitamin C (DAV) – A potent combination therapy for targeting mitochondria and eradicating cancer stem cells
https://dx.doi.org/10.18632%2Faging.101905
Vitamin C and Doxycycline – A synthetic lethal combination therapy targeting metabolic flexibility in cancer stem cells (CSCs)
https://dx.doi.org/10.18632%2Foncotarget.18428
The antiparasitic drug niclosamide inhibits dengue virus infection by interfering with endosomal acidification independent of mTOR
https://doi.org/10.1371/journal.pntd.0006715
NSAID celecoxib – a potent mitochondrial pro-oxidant cytotoxic agent sensitizing metastatic cancers and cancer stem cells to chemotherapy
http://dx.doi.org/10.20517/2394-4722.2018.42
Treatment of hepato carcinoma with celecoxib and pentoxifylline – a
case report
β-Elemene Induces Apoptosis in Human Renal-cell Carcinoma 786-0 Cells through Inhibition of MAPK ERK and PI3K Akt mTOR Signalling Pathways
http://dx.doi.org/10.7314/APJCP.2012.13.6.2739
Inhibitory effect of β-elemene on human breast cancer cells
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4129006/
Anti-Cancer Properties of Nigella Sativa Essential Oils and their Major Constituents, Thymoquinone and beta-Elemene
https://doi.org/10.2174/157488409787236137
Repurposed drugs schema – Astrocytoma
Cannabinoid-induced cell death in endometrial cancer cells- involvement of TRPV1 receptors in apoptosis
https://link.springer.com/article/10.1007/s13105-018-0611-7
β-elemene against Burkitt’s lymphoma via activation of PUMA mediated apoptotic pathway
https://doi.org/10.1016/j.biopha.2018.07.124
Pentoxifylline-Induced Apoptosis in Chronic Lymphocytic Leukemia – New Insights into Molecular Mechanism
https://doi.org/10.2174/1389557517666171002162258
Synergistic promoting effects of pentoxifylline and simvastatin on the apoptosis of triple-negative MDA-MB-231 breast cancer cells
https://doi.org/10.3892/ijo.2018.4272
Melatonin‐mediated regulation of autophagy – Making sense of double‐edged sword in cancer
https://doi.org/10.1002/jcp.28435
Melatonin – A new inhibitor agent for cervical cancer treatment
https://doi.org/10.1002/jcp.28865
Immunoregulatory role of melatonin in cancer
https://doi.org/10.1002/jcp.29036
Melatonin inhibits lung metastasis of gastric cancer in vivo
https://doi.org/10.1016/j.biopha.2019.109018
Clock genes and the role of melatonin in cancer cells
https://doi.org/10.32794/mr11250026
Melatonin as a potential inhibitor of colorectal cancer
http://dx.doi.org/10.1002/jcb.28833
Melatonin and non-small cell lung cancer
https://doi.org/10.1186/s12935-019-0853-7
Melatonin enhances TNF-α-mediated cervical cancer HeLa cells death
https://doi.org/10.1186/s12935-019-0777-2
Metformin as an anti-cancer agent – actions and mechanisms targeting cancer stem cells
https://doi.org/10.1093/abbs/gmx106
The Endocannabinoid System, Our Universal Regulator
https://www.jyi.org/2018-june/2018/6/1/the-endocannabinoid-system-our-universal-regulator
Targeting colon cancer stem cells with novel blood cholesterol drug pitavastatin
https://www.europeanreview.org/article/12394
Pitavastatin suppressed liver cancer cells in vitro and in vivo
http://dx.doi.org/10.2147/OTT.S106906
Proscillaridin A induces apoptosis and suppresses non-small-cell lung cancer tumor growth via calcium-induced DR4 upregulation
https://www.nature.com/articles/s41419-018-0733-4
Heart failure drug proscillaridin A targets MYC overexpressing leukemia through global loss of lysine acetylation
https://doi.org/10.1186/s13046-019-1242-8
Proscillaridin A is cytotoxic for glioblastoma cell lines and controls tumor xenograft growth in vivo
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4279420/
Proscillaridin A Promotes Oxidative Stress and ER Stress, Inhibits STAT3 Activation, and Induces Apoptosis in A549 Lung Adenocarcinoma Cells
https://doi.org/10.1155/2018/3853409
Proscillaradin A – From Cardiac Glycosides to Cancer Therapeutics
http://dx.doi.org/10.17582/journal.pujz/2018.33.2.205.209
Metformin combined with aspirin significantly inhibit pancreatic cancer cell growth in vitro and in vivo by suppressing anti-apoptotic proteins Mcl-1 and Bcl-2
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673260/
A Novel High Content Imaging-Based Screen Identifies the Anti-Helminthic Niclosamide as an Inhibitor of Lysosome Anterograde Trafficking and Prostate Cancer Cell Invasion
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0146931
Berberine Inhibits the Metastatic Ability of Prostate Cancer Cells
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278877/
Metformin and Prostate Cancer – a New Role for an Old Drug
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405102/
Evaluation of Cytotoxic Effects and Underlying Mechanisms of Disulfiram on Breast Cancer Cell Lines
https://refubium.fu-berlin.de/handle/fub188/23438
Evaluation of the Cytotoxic and Autophagic Effects of Atorvastatin on MCF-7 Breast Cancer Cells
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5981123/
Repurposing disulfiram for treatment of Staphylococcus aureus infections
https://doi.org/10.1016/j.ijantimicag.2019.03.024
Disulfiram (Antabuse) Activates ROS-Dependent ER Stress and Apoptosis in Oral Cavity Squamous Cell Carcinoma
https://www.mdpi.com/2077-0383/8/5/611
Disulfiram (Tetraethylthiuram Disulfide) in the Treatment of Lyme Disease and Babesiosis
http://dx.doi.org/10.3390/antibiotics8020072
Preclinical and Clinical Assessment of Cannabinoids as Anti-Cancer Agents
http://dx.doi.org/10.3389/fphar.2016.00361
Novel combination of thymoquinone and resveratrol enhances anticancer effect on hepatocellular carcinoma cell line
https://doi.org/10.1016/j.fjps.2017.08.001
Recent advances on the anti-cancer properties of Nigella sativa, a widely used food additive
http://dx.doi.org/10.1016/j.jaim.2016.07.004
Antitumor effect of thymoquinone combined with resveratrol on mice transplanted with breast cancer
http://dx.doi.org/10.1016/j.apjtm.2017.03.026
Thymoquinone antioxidant pro-oxidant effect as potential anticancer remedy
https://doi.org/10.1016/j.biopha.2019.108783
β‐Caryophyllene, the major constituent of copaiba oil, reduces systemic inflammation and oxidative stress
https://onlinelibrary.wiley.com/doi/10.1002/jcb.27369
Anti-tumor and Anti-angiogenic Effects of Aspirin-PC in Ovarian Cancer
http://mct.aacrjournals.org/content/early/2016/09/16/1535-7163.MCT-16-0074
Antitumor Effect of Albendazole on Cutaneous Squamous Cell Carcinoma (SCC) Cells
https://doi.org/10.1155/2019/3689517
The Natural Occurring Compounds Targeting Endoplasmic Reticulum Stress
http://dx.doi.org/10.1155/2016/7831282
microRNAs and cancer metabolism reprogramming: the paradigm of metformin
http://dx.doi.org/10.3978/j.issn.2305-5839.2014.06.03
Fenbendazole acts as a moderate microtubule destabilizing agent and causes cancer cell death by modulating multiple cellular pathways
https://www.nature.com/articles/s41598-018-30158-6
Benzimidazoles Downregulate Mdm2 and MdmX and Activate p53 in MdmX Overexpressing Tumor Cells
http://dx.doi.org/10.3390/molecules24112152
Antiproliferative effect of benzimidazole anthelmintics albendazole, ricobendazole, and flubendazole in intestinal cancer cell lines
https://www.ncbi.nlm.nih.gov/pubmed/23884106
Repositioning of the anthelmintic drug mebendazole for the treatment for colon cancer
https://link.springer.com/article/10.1007%2Fs00432-013-1539-5
Unexpected Antitumorigenic Effect of Fenbendazole when Combined with Supplementary Vitamins
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2687140/
The antihelmintic flubendazole inhibits microtubule function through a mechanism distinct from Vinca alkaloids and displays preclinical activity in leukemia and myeloma
http://www.bloodjournal.org/content/115/23/4824
Mutations in tumor suppressor p53 and deregulation of cellular metabolism
https://edoc.hu-berlin.de/handle/18452/20285
Piperlongumine rapidly induces the death of human pancreatic cancer cells mainly through the induction of ferroptosis
https://www.spandidos-publications.com/10.3892/ijo.2018.4259
Piperlongumine induces autophagy by targeting p38 signaling
https://www.nature.com/articles/cddis2013358
Piperlongumine induces apoptosis and autophagy in human lung cancer cells through inhibition of PI3K Akt mTOR pathway
https://doi.org/10.1177%2F0394632015598849
MECHANISMS OF PIPERLONGUMINE-INDUCED CANCER CELL DEATH
https://library.ndsu.edu/ir/handle/10365/25178
11 Oncologic Emergencies You Need to Know
https://reference.medscape.com/slideshow/oncologic-emergencies-6011636
Lemongrass essential oil and citral inhibit Src Stat3 activity and suppress the proliferation survival of small-cell lung cancer cells, alone or in combination with chemotherapeutic agents
https://www.spandidos-publications.com/ijo/52/5/1738
Drug Repurposing for the Treatment of Acute Myeloid Leukemia
https://doi.org/10.3389/fmed.2017.00211
The Anthelmintic Flubendazole Blocks Human Melanoma Growth and Metastasis and Suppresses Programmed Cell Death Protein-1 and Myeloid-Derived Suppressor Cell Accumulation
https://doi.org/10.1016/j.canlet.2019.05.026
Mebendazole for Differentiation Therapy of Acute Myeloid Leukemia Identified by a Lineage Maturation Index
http://dx.doi.org/10.1101/688192
Seaweeds-derived compounds modulating effects on signal transduction pathways – A systematic review
https://doi.org/10.1016/j.phymed.2019.153016
Thymoquinone enhanced the tumoricidal activity of NK Cells against Lung Cancer
https://www.jimmunol.org/content/200/1_Supplement/124.5
Recent advances on the anti-cancer properties of Nigella sativa, a widely used food additive
http://dx.doi.org/10.1016/j.jaim.2016.07.004
Anatomy of the Lymphatic and Immune Systems
Extract of Cordyceps militaris inhibits angiogenesis and suppresses tumor growth of human malignant melanoma cells
https://www.spandidos-publications.com/ijo/45/1/209
Apoptosis and inhibition of proliferation of cancer cells induced by cordycepin
https://www.spandidos-publications.com/10.3892/ol.2015.3273
The Anticancer Properties of Cordycepin and Their Underlying Mechanisms
http://dx.doi.org/10.3390/ijms19103027
Oridonin Targets Multiple Drug-Resistant Tumor Cells as Determined by in Silico and in Vitro Analyses
https://www.frontiersin.org/articles/10.3389/fphar.2018.00355/full
Anticancer and antimetastatic effects of cordycepin, an active component of Cordyceps sinensis
http://dx.doi.org/10.1016/j.jphs.2014.09.001
Cordycepin induces apoptotic cell death of human brain cancer through the modulation of autophagy
http://dx.doi.org/10.1016/j.tiv.2017.10.002
Disulfiram – AGENT FOR CONTROLLING CELLS CONSTITUTING CANCER MICROENVIRONMENT OR INFLAMMATORY MICROENVIRONMENT
https://patents.google.com/patent/US20180000755A1/en
Microbiota-Derived Short-Chain Fatty Acids Promote the Memory Potential of Antigen-Activated CD8 + T Cells
https://doi.org/10.1016/j.immuni.2019.06.002
Disulfiram with or without metformin inhibits oesophageal squamous cell carcinoma in vivo
https://doi.org/10.1016/j.canlet.2017.12.026
Eradication of spontaneous malignancy by local immunotherapy
https://stm.sciencemag.org/content/10/426/eaan4488.short
Vitamin D signalling pathways in cancer: potential for anticancer therapeutics
https://doi.org/10.1038/nrc2196
High Dose Intravenous Vitamin C and Long Time Survival of a Patient With Cancer of Head of the Pancreas
http://www.orthomolecular.org/library/jom/1995/pdf/1995-v10n02-p087.pdf
Mechanisms of anti-cancer effects of ascorbate – Cytotoxic activity and epigenetic modulation
http://dx.doi.org/10.1016/j.bcmd.2017.09.005
Effect of high-dose intravenous vitamin C on inflammation in cancer patients
http://www.translational-medicine.com/content/10/1/189
Vitamin C selectively kills KRAS and BRAF mutant colorectal cancer cells by targeting GAPDH
https://science.sciencemag.org/content/350/6266/1391
Hydrocortisone, Vitamin C, and Thiamine for the Treatment of Severe Sepsis and Septic Shock
https://doi.org/10.1016/j.chest.2016.11.036
Vitamin C preferentially kills cancer stem cells in hepatocellular carcinoma via SVCT-2
https://doi.org/10.1038/s41698-017-0044-8
Alcohol-abuse drug disulfiram targets cancer via p97 segregase adaptor NPL4
http://www.nature.com/doifinder/10.1038/nature25016
Disulfiram Facilitates Intracellular Cu Uptake and Induces Apoptosis in Human Melanoma Cells
https://pubs.acs.org/doi/abs/10.1021/jm049568z
Targeting flavin‐containing enzymes eliminates cancer stem cells (CSCs), by inhibiting mitochondrial respiration – Vitamin B2 (Riboflavin)
in cancer therapy
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5764395/
Magnolol induces apoptosis via caspase-independent pathwaysin non-small cell lung cancer cells
https://www.sci-hub.se/10.1007/s12272-013-0232-1
Disulfiram targeting lymphoid malignant cell lines via ROS-JNK activation as well as Nrf2 and NF-kB pathway inhibition
http://www.translational-medicine.com/content/12/1/163
Targeting autophagy inhibits melanoma growth by enhancing NK cells infiltration in a CCL5-dependent manner
http://www.pnas.org/cgi/doi/10.1073/pnas.1703921114
Honokiol exhibits enhanced antitumor effects with chloroquine by inducing cell death and inhibiting autophagy in human non-small cell lung cancer cells
https://www.spandidos-publications.com/10.3892/or.2015.4091
Autophagy inhibition overcomes multiple mechanisms of resistance to BRAF inhibition in brain tumors
http://dx.doi.org/10.7554/eLife.19671
NF-κB activation induced by chloroquine requires autophagosome, p62, and JNK signaling and promotes tumor cell resistance
http://www.jbc.org/content/292/8/3379
Disulfiram combined with copper inhibits metastasis and epithelial–mesenchymal transition in hepatocellular carcinoma through the NF-jB and TGF-b pathways
https://doi.org/10.1111/jcmm.13334
Evidence for the efficacy of disulfiram and copper combination in glioblastoma multiforme – A propos of a case
https://www.jbuon.com/archive/22-5-1227.pdf
Repositionierung von Disulfiram zur Therapie des Ovarialkarzinoms
https://edoc.ub.uni-muenchen.de/20629/7/Papaioannou_Margarita.pdf
Disulfiram copper selectively eradicates AML leukemia stem cells in vitro and in vivo by simultaneous induction of ROS-JNK and inhibition of NF-κB and Nrf2
http://dx.doi.org/10.1038/cddis.2017.176
Disulfiram modulated ROS–MAPK and NFkB pathways and targeted breast cancer cells with cancer stem cell-like properties
https://www.nature.com/articles/bjc2011126
Pentoxifylline inhibits melanoma tumor growth and angiogenesis by targeting STAT3 signaling pathway
http://dx.doi.org/10.1016/j.biopha.2013.03.020
Anticancer adjuvant containing pentoxifylline Patent US 20150374702
https://patents.google.com/patent/US20150374702
Potentiation of Anticancer Drugs: Effects of Pentoxifylline on Neoplastic Cells
https://www.mdpi.com/1422-0067/13/1/369
Pentoxifylline triggers autophagy via ER stress response that interferes
with Pentoxifylline induced apoptosis in human melanoma cells
http://dx.doi.org/10.1016/j.bcp.2015.12.018
Pentoxifylline- rescue for the oncological patient. Anticancer and protective properties of an alkaloid derivative
https://pdfs.semanticscholar.org/51b4/7e2be711fbe3666721bc7829aebb07246c2b.pdf
Disulfiram Induces Apoptosis in Human Melanoma Cells: A Redox-related Process
http://mct.aacrjournals.org/content/1/3/197.long
The Efficacy of Dandelion Root Extract in Inducing Apoptosis in Drug-Resistant Human Melanoma Cells
https://www.hindawi.com/journals/ecam/2011/129045/
Ligands for cannabinoid receptors, promising anticancer agents
http://dx.doi.org/10.1016/j.lfs.2015.12.053
beta-Caryophyllene oxide inhibits growth and induces apoptosis through the suppression of PI3K/AKT/mTOR/S6K1 pathways and ROS-mediated MAPKs activation
http://dx.doi.org/10.1016/j.canlet.2011.08.001
A Brief Overview on Natural Killer Cells
http://dx.doi.org/10.5772/intechopen.72328
Anti-hepatocellular carcinoma properties of the anti-alcoholism drug disulfiram discovered to enzymatically inhibit the AMPK
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342717/
Lung cancer stem cells: The root of resistance
http://dx.doi.org/10.1016/j.canlet.2016.01.012
CANNABIS for the treatment of cancer – The anticancer activity of phytocannabinoids and endocannabinoids – by Justin Kander
http://www.marine-science.news/Cannabis_and_Cancer.pdf
Reexamining cancer metabolism: lactate production for carcinogenesis could be the purpose and explanation of the Warburg Effect
https://academic.oup.com/carcin/article/38/2/119/2709442
Dietary ω-3 Polyunsaturated Fatty Acids Inhibit Tumor Growth in Transgenic Apc Min + Mice, Correlating with CB1 Receptor Up-Regulation
https://www.mdpi.com/1422-0067/18/3/485
Oleocanthal rapidly and selectively induces cancer cell death via lysosomal membrane permeabilization
http://dx.doi.org/10.1080/23723556.2015.1006077
Oleocanthal: A Naturally Occurring Anti-Inflammatory Agent in Virgin Olive Oil
Oleocanthal Attenuates Cell Proliferation, Invasiveness, and Tumor Growth in Breast Cancer Models
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0097622
Oleocanthal inhibits growth and metastasis by blocking activation of STAT3 in human hepatocellular carcinoma
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5190038/
TARGETING THE CANCER METABOLIC PHENOTYPE USING HIGH DOSE VITAMIN B1 THERAPY
https://pdfs.semanticscholar.org/8587/9ad67d0576b44157f83a954f3ae72cbb7b74.pdf
High‑dose vitamin B1 reduces proliferation in cancer cell lines analogous to dichloroacetate
http://dx.doi.org/DOI:10.1007/s00280-014-2386-z
Oxidative stress and apoptosis induction in human thyroid carcinoma cells exposed to the essential oil from Pistacia lentiscus aerial parts (Mastic oil)
http://dx.doi.org/DOI:10.1371/journal.pone.0172138
Epigenetic mechanisms and endocannabinoid signalling
https://doi.org/10.1111/febs.12125
The endocannabinoid signaling system in cancer
http://dx.doi.org/10.1016/j.tips.2013.03.003
In Vitro Investigation of the Potential Immunomodulatory and Anti-Cancer Activities of Black Pepper (Piper nigrum) and Cardamom (Elettaria cardamomum)
https://doi.org/10.1089/jmf.2009.1131
Antiproliferative and Cytotoxic Activity of Xanthohumol and Its Non-Estrogenic Derivatives in Colon and Hepatocellular Carcinoma Cell Lines
http://dx.doi.org/10.3390/ijms20051203
Analyzing bioactive effects of the minor hop compound xanthohumol C on human breast cancer cells using quantitative proteomics
https://doi.org/10.1371/journal.pone.0213469
Xanthohumol increases death receptor 5 expression and enhances apoptosis with the TNF-related apoptosis-inducing ligand in neuroblastoma cell lines
https://doi.org/10.1371/journal.pone.0213776
Oridonin inhibits the proliferation, migration and invasion of human osteosarcoma cells via suppression of matrix metalloproteinase expression and STAT3 signalling pathway
https://jbuon.com/archive/24-3-1175.pdf
The metabolic advantage of tumor cells
http://www.molecular-cancer.com/content/10/1/70
PHYTO-PHARMACOLOGICAL PROFILE OF HUMULUS LUPULUS
https://pdfs.semanticscholar.org/d66f/ea4d38ba8ab88b902fb95112b91da566e217.pdf
Targeted therapy of the AKT kinase inhibits esophageal squamous cell carcinoma growth in vitro and in vivo
https://doi.org/10.1002/ijc.32285
Dexamethasone co-medication in cancer patients undergoing chemotherapy causes substantial immunomodulatory effects with implications for chemo-immunotherapy strategies
http://dx.doi.org/10.1080/2162402X.2015.1066062
Polo-like Kinase 1 inhibition as a therapeutic approach to selectively 1 target BRCA1-deficient cancer cells by synthetic lethality induction
http://dx.doi.org/DOI:10.1158/1078-0432.CCR-18-3516
MTH1 inhibitor TH588 induces mitosis-dependent accumulation of genomic 8-oxodG and disturbs mitotic progression
http://dx.doi.org/10.1101/573931
Inhibition of Tumor Growth by Dietary Indole-3-Carbinol in a Prostate Cancer Xenograft Model May Be Associated with Disrupted Gut Microbial Interactions
http://dx.doi.org/10.3390/nu11020467
COMBINED PHYTOCHEMICALS SYNERGISTICALLY RESTRAIN BREAST CANCER IN CULTURED CELLS AND XENOGRAFT MICE – Indole-3-Carbinol
https://search.proquest.com/openview/e4a698fb1ae574f5e9aa823e6981bea2
Synergistic Anticancer Effects of Silibinin and Chrysin in T47D Breast Cancer Cells
COMBINATIONS OF DRUGS (E.G., A BENZIMIDAZOLE AND PENTAMIDINE) FOR THE TREATMENT OF NEOPLASTIC DSORDERS – U.S. Patent US6693125B2
https://patents.google.com/patent/US6693125B2/en
Role of Melatonin in Cancer Treatment
http://ar.iiarjournals.org/content/32/7/2747.long
Antihelminthic drugs as a treatment for hyperproliferative diseases
https://pdfs.semanticscholar.org/6dd9/332c998979d15a8edadcf721211d936fc8f9.pdf
Psilocybin-assisted mindfulness training modulates self-consciousness and brain default mode network connectivity with lasting effects
https://doi.org/10.1016/j.neuroimage.2019.04.009
Cancer stem cells – Road to therapeutic resistance and strategies to overcome resistance
https://doi.org/10.1016/j.bbadis.2018.11.015
The novel role of pyrvinium in cancer therapy – Pyrvinium and inhibition of Hippo pathway
https://doi.org/10.1002/jcp.26006
Inhibitory effect of pyrvinium pamoate on uveal melanoma cells involves blocking of Wnt/β-catenin pathway
https://academic.oup.com/abbs/article/49/10/890/4097565
Reprofiling a classical anthelmintic, pyrvinium pamoate, as an anti-cancer drug targeting mitochondrial respiration
http://www.frontiersin.org/Oncology/editorialboard
Cytotoxic Effects of Artemisia annua L. and Pure Artemisinin on the D-17 Canine Osteosarcoma Cell Line
https://doi.org/10.1155/2019/1615758
MICROTUBULES AS A TARGET FOR ANTICANCER DRUGS
https://www.nature.com/articles/nrc1317
Melatonin: An important anticancer agent in colorectal cancer
https://onlinelibrary.wiley.com/doi/abs/10.1002/jcp.29049
In vitro investigation of anti-cancer activity of propolis on hepatocellular carcinoma cells
http://www.medicinescience.org/wp-content/uploads/2019/03/53-1547584461MS-2019-01-09.pdf
Effects of caffeic acid phenethyl ester (CAPE) on angiogenesis, apoptosis and oxidatıve stress ın various cancer cell lines
https://doi.org/10.1080/10520295.2019.1589574
Hibiscus flower extract selectively induces apoptosis in breast cancer cells and positively interacts with common chemotherapeutics
https://doi.org/10.1186/s12906-019-2505-9
Anticancer Activity and Underlying Mechanism of Phytochemicals against Multiple Myeloma
http://dx.doi.org/10.3390/ijms20092302
Insights on the Multifunctional Activities of Magnolol
https://doi.org/10.1155/2019/1847130
Grape seed procyanidin B2 promotes the autophagy and apoptosis in colorectal cancer cells via regulating PI3K Akt signaling pathway
http://doi.org/10.2147/OTT.S195615
Anti-cancer effects of cinnamon – Insights into its apoptosis effects
https://doi.org/10.1016/j.ejmech.2019.05.067
Marine Carotenoid Fucoxanthin Possesses Anti-Metastasis Activity – Molecular Evidence
http://dx.doi.org/10.3390/md17060338
Pharmacoepigenetics of Chinese Herbal Components in Cancer
https://doi.org/10.1016/B978-0-12-813939-4.00035-8
Suppression of colorectal cancer cell growth by combined treatment of 6‑gingerol and γ‑tocotrienol via alteration of multiple signalling pathways
https://doi.org/10.1007/s11418-019-01323-6
Natural products for treating colorectal cancer – A mechanistic review
https://doi.org/10.1016/j.biopha.2019.109142
Kaempferol exerts anti-proliferative effects on human ovarian cancer cells by inducing apoptosis, G0 G1 cell cycle arrest and modulation of MEK/ERK and STAT3 pathways
https://jbuon.com/archive/24-3-975.pdf
Icariin inhibits the growth of human cervical cancer cells by inducing apoptosis and autophagy by targeting mTOR PI3K AKT signalling pathway
https://jbuon.com/archive/24-3-990.pdf
Fucoidan from Fucus vesiculosus inhibits new blood vessel formation and breast tumor growth in vivo
https://doi.org/10.1016/j.carbpol.2019.115034
Bioactive Compounds and Biological Functions of Garlic (Allium sativum)
http://dx.doi.org/10.3390/foods8070246
Effects of Curcumin on Ion Channels and Pumps
https://iubmb.onlinelibrary.wiley.com/doi/abs/10.1002/iub.2054
Cardamonin Induces Cell Cycle Arrest, Apoptosis and Alters Apoptosis Associated Gene Expression in WEHI-3 Mouse Leukemia Cells
http://dx.doi.org/10.1142/S0192415X19500332
Honokiol induces apoptosis and suppresses migration and invasion of ovarian carcinoma cells via AMPK/mTOR signaling pathway
https://www.spandidos-publications.com/10.3892/ijmm.2019.4122
Honokiol Eliminates Glioma/Glioblastoma Stem Cell-Like Cells via JAK-STAT3 Signaling and Inhibits Tumor Progression by Targeting Epidermal Growth Factor Receptor
http://dx.doi.org/10.3390/cancers11010022
Dysregulated YAP1/TAZ and TGF-β signaling mediate hepatocarcinogenesis in Mob1a/1b-deficient mice – Ivermectin
http://www.pnas.org/cgi/doi/10.1073/pnas.1517188113
Antibiotic ivermectin selectively induces apoptosis in chronic myeloid leukemia through inducing mitochondrial dysfunction and oxidative stress
https://doi.org/10.1016/j.bbrc.2018.02.063
Antibiotic ivermectin preferentially targets renal cancer through inducing mitochondrial dysfunction and oxidative damage
http://dx.doi.org/10.1016/j.bbrc.2017.08.097
Cimetidine as an anti-cancer agent
Food effect on pharmacokinetics of cannabidiol oral capsules in adult patients with refractory epilepsy
https://onlinelibrary.wiley.com/doi/abs/10.1111/epi.16093
Antibiotic ivermectin selectively induces apoptosis in chronic myeloid leukemia through inducing mitochondrial dysfunction and oxidative stress
https://doi.org/10.1016/j.bbrc.2018.02.063
Anthelmintic drug ivermectin inhibits angiogenesis, growth and survival of glioblastoma through inducing mitochondrial dysfunction and oxidative stress
http://dx.doi.org/10.1016/j.bbrc.2016.10.064
The anti parasitic agent ivermectin induces chloride-dependent membrane hyperpolarization and cell death in leukemia cells
https://doi.org/10.1182/blood-2010-01-262675
Ivermectin induces cell cycle arrest and apoptosis of HeLa cells via mitochondrial pathway
https://doi.org/10.1111/cpr.12543
Ivermectin as an inhibitor of cancer stem‑like cells
https://www.spandidos-publications.com/10.3892/mmr.2017.8231
Ivermectin – Old Drug, New Tricks
http://dx.doi.org/10.1016/j.pt.2017.02.004
The multitargeted drug ivermectin – from an antiparasitic agent to a repositioned cancer drug
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835698/
Doxycycline, salinomycin, monensin and ivermectin repositioned as cancer drugs
https://doi.org/10.1016/j.bmcl.2019.04.045
Gut microbiota, inflammation and colorectal cancer
http://dx.doi.org/10.1016/j.gendis.2016.03.004
Cellular metabolism in colorectal carcinogenesis: Influence of lifestyle, gut microbiome and metabolic pathways
http://dx.doi.org/10.1016/j.canlet.2014.02.026
α‑MMC and MAP30, two ribosome‑inactivating proteins extracted from Momordica charantia, induce cell cycle arrest and apoptosis in A549 human lung carcinoma cells
https://www.spandidos-publications.com/10.3892/mmr.2015.3176
Momordica charantia, a Nutraceutical Approach for Inflammatory Related Diseases
https://doi.org/10.3389/fphar.2019.00486
Tocopherol or combinations of vitamin E forms induce cell death in human prostate cancer cells by interrupting sphingolipid synthesis
http://www.pnas.org?cgi?doi?10.1073?pnas.0408340102
Induction of Tumor Cytotoxic Immune Cells Using a Protein from the Bitter Melon (Momordica charantia)
https://doi.org/10.1016/0008-8749(90)90321-H
Momordica charantia Extract Induces Apoptosis in Human Cancer Cells through Caspase- and Mitochondria-Dependent Pathways
https://www.hindawi.com/journals/ecam/2012/261971/
MOMORDICA CHARANTIA LINN. (KARELA) – NATURE’S SILENT HEALER
Momordicoside G Regulates Macrophage Phenotypes to Stimulate Efficient Repair of Lung Injury and Prevent Urethane-Induced Lung Carcinoma Lesions
https://doi.org/10.3389/fphar.2019.00321
Vitamin E – Regulatory Role on Signal Transduction
https://doi.org/10.1002/iub.1986
Natural Forms of Vitamin E and Metabolites – Regulation of Cancer Cell Death and Underlying Mechanisms
https://doi.org/10.1002/iub.1978
Fucoxanthin induces apoptosis in human glioma cells by triggering ROS-mediated oxidative damage and regulating MAPKs and PI3K AKT pathways
https://pubs.acs.org/doi/10.1021/acs.jafc.8b07126
Icaritin – A Novel Natural Candidate for Hematological Malignancies Therapy
https://doi.org/10.1155/2019/4860268
Albendazole Induces Cell Death in Human Colorectal Cancer Cell Line HT-29
Flubendazole elicits anti-metastatic effects in triple-negative breast cancer via STAT3 inhibition
https://doi.org/10.1002/ijc.31585
Repositioning of drugs for intervention in tumor progression and metastasis: Old drugs for new targets
http://dx.doi.org/doi:10.1016/j.drup.2016.03.002
Flubendazole inhibits glioma proliferation by G2 M cell cycle arrest and pro-apoptosis
https://www.nature.com/articles/s41420-017-0017-2
A list of studies about CBD and Cannabinoids
https://www.themcaa.net/list-of-cbds–cannabis-studies.html#
More Scientific Studies Proving Cannabis Fights Cancer:
Cannabis can kill cancer cells!
- http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1576089
- http://www.ncbi.nlm.nih.gov/pubmed/20090845
- http://www.ncbi.nlm.nih.gov/pubmed/616322
- http://www.ncbi.nlm.nih.gov/pubmed/14640910
- http://www.ncbi.nlm.nih.gov/pubmed/19480992
- http://www.ncbi.nlm.nih.gov/pubmed/15275820
- http://www.ncbi.nlm.nih.gov/pubmed/15638794
- http://www.ncbi.nlm.nih.gov/pubmed/16818650
- http://www.ncbi.nlm.nih.gov/pubmed/17952650
- http://www.ncbi.nlm.nih.gov/pubmed/20307616
- http://www.ncbi.nlm.nih.gov/pubmed/16616335
- http://www.ncbi.nlm.nih.gov/pubmed/16624285
- http://www.ncbi.nlm.nih.gov/pubmed/10700234
- http://www.ncbi.nlm.nih.gov/pubmed/17675107
- http://www.ncbi.nlm.nih.gov/pubmed/14617682
- http://www.ncbi.nlm.nih.gov/pubmed/17342320
- http://www.ncbi.nlm.nih.gov/pubmed/16893424
- http://www.ncbi.nlm.nih.gov/pubmed/15026328
Uterine, testicular, and pancreatic cancers
- http://www.cancer.gov/cancertopics/pdq/cam/cannabis/healthprofessional/page4
- http://www.ncbi.nlm.nih.gov/pubmed/20925645
Brain cancer
Mouth and throat cancer
Breast cancer
- http://www.ncbi.nlm.nih.gov/pubmed/18454173
- http://www.ncbi.nlm.nih.gov/pubmed/16728591
- http://www.ncbi.nlm.nih.gov/pubmed/9653194
Lung cancer
- http://www.ncbi.nlm.nih.gov/pubmed/25069049
- http://www.ncbi.nlm.nih.gov/pubmed/22198381?dopt=Abstract
- http://www.ncbi.nlm.nih.gov/pubmed/21097714?dopt=Abstract
Prostate cancer
- http://www.ncbi.nlm.nih.gov/pubmed/12746841?dopt=Abstract
- http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339795/?tool=pubmed
- http://www.ncbi.nlm.nih.gov/pubmed/22594963
- http://www.ncbi.nlm.nih.gov/pubmed/15753356
- http://www.ncbi.nlm.nih.gov/pubmed/10570948
- http://www.ncbi.nlm.nih.gov/pubmed/19690545
Blood cancer
Skin cancer
Liver cancer
Cannabis cancer cures (general)
- http://www.ncbi.nlm.nih.gov/pubmed/12514108
- http://www.ncbi.nlm.nih.gov/pubmed/15313899
- http://www.ncbi.nlm.nih.gov/pubmed/20053780
- http://www.ncbi.nlm.nih.gov/pubmed/18199524
- http://www.ncbi.nlm.nih.gov/pubmed/19589225
- http://www.ncbi.nlm.nih.gov/pubmed/12182964
- http://www.ncbi.nlm.nih.gov/pubmed/19442435
- http://www.ncbi.nlm.nih.gov/pubmed/12723496
- http://www.ncbi.nlm.nih.gov/pubmed/16250836
- http://www.ncbi.nlm.nih.gov/pubmed/17237277
Cancers of the head and neck
Cholangiocarcinoma cancer
Leukemia
- http://www.ncbi.nlm.nih.gov/pubmed/15454482
- http://www.ncbi.nlm.nih.gov/pubmed/16139274
- http://www.ncbi.nlm.nih.gov/pubmed/14692532
Cannabis partially/fully induced cancer cell death
- http://www.ncbi.nlm.nih.gov/pubmed/12130702
- http://www.ncbi.nlm.nih.gov/pubmed/19457575
- http://www.ncbi.nlm.nih.gov/pubmed/18615640
- http://www.ncbi.nlm.nih.gov/pubmed/17931597
- http://www.ncbi.nlm.nih.gov/pubmed/18438336
- http://www.ncbi.nlm.nih.gov/pubmed/19916793
- http://www.ncbi.nlm.nih.gov/pubmed/18387516
- http://www.ncbi.nlm.nih.gov/pubmed/15453094
- http://www.ncbi.nlm.nih.gov/pubmed/19229996
- http://www.ncbi.nlm.nih.gov/pubmed/9771884
- http://www.ncbi.nlm.nih.gov/pubmed/18339876
- http://www.ncbi.nlm.nih.gov/pubmed/12133838
- http://www.ncbi.nlm.nih.gov/pubmed/16596790
- http://www.ncbi.nlm.nih.gov/pubmed/11269508
- http://www.ncbi.nlm.nih.gov/pubmed/15958274
- http://www.ncbi.nlm.nih.gov/pubmed/19425170
- http://www.ncbi.nlm.nih.gov/pubmed/17202146
- http://www.ncbi.nlm.nih.gov/pubmed/11903061
- http://www.ncbi.nlm.nih.gov/pubmed/15451022
- http://www.ncbi.nlm.nih.gov/pubmed/20336665
- http://www.ncbi.nlm.nih.gov/pubmed/19394652
- http://www.ncbi.nlm.nih.gov/pubmed/11106791
- http://www.ncbi.nlm.nih.gov/pubmed/19189659
- http://www.ncbi.nlm.nih.gov/pubmed/16500647
- http://www.ncbi.nlm.nih.gov/pubmed/19539619
- http://www.ncbi.nlm.nih.gov/pubmed/19059457
- http://www.ncbi.nlm.nih.gov/pubmed/16909207
- http://www.ncbi.nlm.nih.gov/pubmed/18088200
- http://www.ncbi.nlm.nih.gov/pubmed/10913156
- http://www.ncbi.nlm.nih.gov/pubmed/18354058
- http://www.ncbi.nlm.nih.gov/pubmed/19189054
- http://www.ncbi.nlm.nih.gov/pubmed/17934890
- http://www.ncbi.nlm.nih.gov/pubmed/16571653
- http://www.ncbi.nlm.nih.gov/pubmed/19889794
- http://www.ncbi.nlm.nih.gov/pubmed/15361550
Translocation-positive rhabdomyosarcoma
Lymphoma
- http://www.ncbi.nlm.nih.gov/pubmed/18546271
- http://www.ncbi.nlm.nih.gov/pubmed/16936228
- http://www.ncbi.nlm.nih.gov/pubmed/16337199
- http://www.ncbi.nlm.nih.gov/pubmed/19609004
Cannabis kills cancer cells
- http://www.ncbi.nlm.nih.gov/pubmed/16818634
- http://www.ncbi.nlm.nih.gov/pubmed/12648025
- http://www.ncbi.nlm.nih.gov/pubmed/17952650
- http://www.ncbi.nlm.nih.gov/pubmed/16835997