Turmeric Extract Kills Highly Lethal Pancreatic Tumors, Preclinical Study Reveals

September 22, 2013

Considering that the conventional treatment of advanced stage pancreatic cancer can result in as little as a 1% 5-year survival rate, new preclinical research on a liposomal turmeric extract that inhibits pancreatic tumor growth by 42% is all the more amazing.

A promising new study published in the journalAnticancer Research, a peer-reviewed medical journal published by the International Institute of Anticancer Research, reveals a unique turmeric extract known asliposomal curcuminmay provide an ideal chemotherapy alternative in the treatment of highly lethal pancreatic cancers.[1]

Curcumin is the primarly polyphenol inturmeric, and has been the subject of extensive research demonstrating its ability to kill cancer cells, with over 1,500 studies available to view on Greenmedinfo.com relevant to over 100 distinct cancer types, including 24 studiesdemonstrating its anti-pancreatic cancerproperties. [View all thecurcumin studies.]

Liposomal curcumin utilizes a successful lipid-based drug delivery system, with some liposomal formulations having already received FDA approval.  Owing to curcumin’s low water solubility and subsequent low systemic bioavailability, its encapsulation into liposomes (artificially-prepared vesicle composed of a lipid bilayer) greatly improves its ability to gain entry into the body by passing through the ‘glucoronidation barrier’ in the liver.

Exocrine pancreatic cancer is notorious for responding poorly to conventional treatment, with American Cancer Society statistics promising only a 14% 5-year survival rate in Stage IA cancers, spiraling down to only 1% for Stage IV types.[2]  Moreover, even when chemotherapy, surgery andradiotherapyresults in the successful debulking of the tumor, and the patient manages to survive past 5 years, recurrence is still common; this often occurs as a direct result of conventional treatment, which damages the immune system and enriches the treatment-resistance tumorigeniccancer stem cellpopulation within the post-treatment cancer survivor’s body.

The new study was performed by researchers at the Department of Molecular Biology and Immunology, and Institute for Cancer Research, University of North Texas Health Science Center, Fort Worth, Texas. They determined the antitumor effects of a liposomal curcumin formulation against human pancreatic cancer cells through in vitro and xenograft studies, where the cells were implanted into mice to form tumors

The liposomal curcumin formulation was found to inhibit pancreatic cancer cell proliferation in vitro, and when administered to the animals intraperitoneally at a dose of 20 mg/kg, three-times a week for four weeks, a 42% suppression of tumor growth was observed compared to untreated controls.  This would be the equivalent of 1,360 mg for a 150 lb adult.  Note, the 20 mg/kg dose given to the test animals is 100 times lower than the LD50 for mice (i.e. the dose that would take to kill 50% of a test group).

Additionally, researchers observed “A potentantiangiogenic effect,” characterized by a reduced number blood vessels and other pro-angiogenic factors associated with the growth of the tumor’s blood supply.

The researchers concluded,“These data clearly establish the efficacy of liposomal curcumin in reducing human pancreatic cancer growth in the examined model. The therapeutic curcumin-based effects, with no limiting side-effects, suggest that liposomal curcumin may be beneficial in patients with pancreatic cancer.”

Considering the relatively high safety margin, affordability, accessibility and effectiveness (as demonstrated by pre-clinical research and a vast body of anecdotes) of turmeric extracts in fighting highly lethal cancers, we can only hope the medical establishment begins to incorporate these medicinal spices into their treatment protocols.  Considering how potent are thechemosensitizing effectsof curcumin, it could be argued that it isunethical for them not to provide their patients the option of using these agents, or at the very least as adjuvants in integrative cancer care.
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