Dr. Adem's Natural Treatment for Stomach Cancer
Stomach cancer is considered the second most common cause of cancer deaths in men and the fourth com...
by Dr. Adem Gunes
Stomach cancer is one of the deadliest cancers in the world. It requires special attention and appropriate, timely treatment.
Researchers have now put forward the benefits of some natural supplements in the treatment of stomach cancer:
Aloe vera is a medicinal plant. Aloe vera seems to prove beneficial in the treatment of stomach cancer. It kills H. pylori bacteria.
Approximately 90% of patients with gastric cancer have H. pylori bacteria in their stomach. It also inhibits acid secretion from the stomach.
Excess acid production causes gastritis. H. Pylori bacteria enhance inflammation in the stomach. Aloe vera prevents inflammation by many different means.
Some of the ingredients that are found in aloe vera may have helpful effects on the body’s immune system and can shrink the size of cancers.
Studies show that patients taking the aloe vera with chemotherapy had an improved quality of life, and they had less chemotherapy side effects for example fatigue and numb fingers.
There are no side effects from the aloe vera. Patients taking the aloe vera have three years increased survival than patients who are on only chemotherapy.
Black cumin seeds have been used for centuries to treat a variety of diseases. Its scientific name is “Nigella sativa.”
The crude oil and thymoquinone (TQ) obtained from its seeds are effective against several diseases like cancer, diabetes mellitus, cardiovascular complications, kidney disease, asthma, etc.
Research suggests that the black seed is an effective anti-tumor treatment for stomach cancer. Black cumin, have experimented in the lab and found to have potent anti-cancer and antioxidant effects.
Antioxidants are the chemicals that clear the body of free radicals that cause cell damage and stimulate the disease.
The oil, extract or TQ component can destroy the cancer cells and protect the healthy tissues during treatment.
Curcumin is a polyphenol extracted from the plant Curcuma longa, generally called turmeric. It is also called diferuloylmethane.
Extensive research of the last 50 years has showed that this polyphenol can both treat and prevent cancer. Several studies suggest that curcumin have massive potential in the prevention and therapy of stomach cancer.
It prevents development and production of stomach cancer and effective in controlling cancers that are resistant to the chemotherapy.
Chronic gastritis with the Helicobacter pylori (H. pylori) infection is the main cause of stomach cancer.
Curcumin prevents the development and growth of H. pylori and stops the conversion of stomach cells into cancer cells. Curcumin is considered safe and has no side effects.
Epigallocatechin gallate, or EGCG, is an antioxidant present in tea. Tea is one of the most extensively consumed beverages, second only to water.
The cancer-defending effects of green tea have been stated in several studies. Cancer rates are low in countries, for example, Japan where green tea is taken on a regularly.
Several animal and clinical studies suggest that EGCG play a significant role in the prevention of stomach cancer.
It has been recommended that EGCG and other tea constituents such as catechin suppress the progression of the tumor by inhibiting the tumor factors release.
The exposure of human stomach cells to EGCG results in both growth inhibition and the stimulation of programmed cell death (apoptosis).
EGCG can prevent DNA impairment caused by free radicals. DNA impairment and damage can cause cells to breakdown and leads to several health problems including cancer.
Researches involving large populations of people recommend that drinking green tea is associated with a decreased risk of some cancer types.
Quercetin is a plant-based chemical that is also known as a flavonoid. It is a dietary antioxidant found in many plants and foods. It is an important component present in berries, red wine, buckwheat tea, onion, green tea, and apples.
Quercetin is used as a medicine. It has some anti-proliferative activities against gastric cancer. Quercetin is a cancer chemopreventive agent that prevents tumor promotion by causing cell cycle stop and promoting cell death.
Quercetin appears to have little toxicity when administered orally or intravenously.
Resveratrol is a naturally occurring polyphenol with potent anti-cancer activity. It has since been found in many plants, including berries, grapes, and peanuts.
Studies suggested that resveratrol causes induction of tumor cell death through reactive oxygen species.
Resveratrol inhibits the proliferation of a large number of cell lines and exhibits anti-cancer properties, by its capability to decrease proliferation of different types of tumor cells, comprising lymphoma, melanoma, multiple myeloma, squamous cell carcinoma, cancers of the prostate, stomach, breast, ovary, cervix, pancreas, colon and thyroid. Resveratrol might produce anti-cancer effects by its antioxidant action.
It causes stimulation of NOS to produce low levels of NO, which, in turn, exert antioxidant action. Consumption of a resveratrol-rich diet is advised because of its protective role against gastric cancer. According to research, resveratrol is pharmacologically safe and have no side effects.
There are some vitamins and supplements that help in stomach cancer and cause enhancement of the immune system. Research shows that vitamin D, fish oils and natural vitamins like vitamin E have anti-cancer effects in Gastrointestinal cancers.
Dr. Adem’s opinion
It is believed that all these natural supplements are a great discovery. It has made cancer treatment easier for the patients due to its multiple benefits.
Cancer specialists are also considering these supplements for the treatment of their patients to get better results. They provide better care by strengthening the immunity and enhancing the effects of other treatments without causing the side effects.
- Therap Adv Gastroenterol. 2012 January; 5(1): 49–69. doi:10.1177/1756283X11410771
- Curr Treat Options Oncol. 2010 Jun;11(1-2):14-23. doi:10.1007/s11864-010-0117-1.
- Ann Surg. 2005 January; 241(1): 27–39. doi: 10.1097/01.sla.0000149300.28588.23
- Proc (Bayl Univ Med Cent). 2004 October; 17(4): 391–399.
- Ann Surg. 1999 August; 230(2): 170.
- Chin J Dig Dis. 2005;6(4):149-54.
- Gan To Kagaku Ryoho. 2009 Aug;36(8):1223-7.
- J Gastroenterol. 2007 Jan;42 Suppl 17:10-5.
- Nihon Rinsho. 2012 Oct;70(10):1720-5.
- Acta Gastroenterol Latinoam. 2007 Jun;37(2):110-7.
- Afr J Tradit Complement Altern Med. 2011; 8(5S): 226–232. doi: 10.4314/ajtcam.v8i5S.10
- Anticancer Res. 2003 Jan-Feb;23(1A):363-98.
- Cell Div. 2008 Oct 3;3:14. doi: 10.1186/1747-1028-3-14.
- World Journal of Gastroenterology 09/2007; 13(31):4255-9.
- Adv Clin Chem. 2011; 53: 155–177.
- Anticancer Res. 2004 Mar-Apr;24(2B):747-53
- Int J Oncol. 2011 May;38(5):1403-8. doi: 10.3892/ijo.2011.951. Epub 2011 Feb 22
- Altern Med Rev 2000;5(3):196-208
- Autophagy. 2011 Sep;7(9):966-78. Epub 2011 Sep 1
- Clin Exp Pharmacol Physiol. 2012 Mar;39(3):227-32. doi: 10.1111/j.1440-1681.2011.05660.x.
- Adv Exp Med Biol. 2008;614:179-86. doi: 10.1007/978-0-387-74911-2_21.
- American Journal of Physiology. Gastrointestinal and Liver Physiology [2002, 282(5):G809-16]
- Anticancer Res. 2004 Sep-Oct;24(5A):2783-840.
- Am J Physiol Gastrointest Liver Physiol 282: G809–G816, 2002. First published January 30, 2002; 10.1152/ajpgi.00193.2001
- Oncol Rep, 5(2):527-9 1998 Mar-Apr.
- Postgrad Med J 2003;79:252–258
- Ann Oncol. 2004 Nov;15(11):1585-95.
- Anticancer Res. 1998 Jan-Feb;18(1B):523-30.
- In Vivo. 2008 May-Jun;22(3):273-8.
- World J Gastroenterol. 2002 Dec;8(6):1023-8.
- Oncologist. 2006 Feb;11(2):136-45.
- Br J Surg. 1995 Sep;82(9):1248-52.
- Gan To Kagaku Ryoho. 2012 Mar;39(3):385-7
- Toxicol In Vitro. 2012 Mar;26(2):221-8. doi: 10.1016/j.tiv.2011.11.015. Epub 2011 Dec 24.