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Study: Chemotherapy Shown to Boost Cancer Growth

chemotherapy drugs

Chemotherapy Drugs

A recent cancer research study, at the Fred Hutchinson Cancer Research Centre in Seattle, has shown that chemotherapy can cause damage to healthy cells which triggers them to secrete a protein that sustains tumour growth and resistance to further treatment.

Researchers in the United States made the “completely unexpected” finding while seeking to explain why cancer cells are so resilient inside the human body when they are easy to kill in the lab. They tested the effects of a type of chemotherapy on tissue collected from men with prostate cancer, and found “evidence of DNA damage” in healthy cells after treatment, the scientists wrote in Nature Medicine.

Chemotherapy works by inhibiting reproduction of fast-dividing cells such as those found in tumours. The scientists found that healthy cells damaged by chemotherapy secreted more of a protein called WNT16B which boosts cancer cell survival.

The protein was taken up by tumour cells neighbouring the damaged cells.

“WNT16B, when secreted, would interact with nearby tumour cells and cause them to grow, invade, and importantly, resist subsequent therapy,” said Nelson.

This protein, it turns out, explains why cancer tumors grow more aggressively following chemotherapy treatments. In essence, chemotherapy turns healthy cells into WNT16B factories which churn out this “activator” chemical that accelerates cancer tumor growth. In cancer treatment, tumours often respond well initially, followed by rapid regrowth and then resistance to further chemotherapy. Rates of tumour cell reproduction have been shown to accelerate between treatments.

The findings of the study were confirmed with prostate cancer, breast cancer and ovarian cancer tumors. This discovery that chemotherapy backfires by accelerating cancer tumor growth is being characterized as “completely unexpected” by scientists.

“Our results indicate that damage responses in benign cells… may directly contribute to enhanced tumour growth kinetics,” wrote the team.

Rather than boosting the immune response of patients, chemotherapy harms the immune system, causing tumors to grow back. This latest researching further confirms what we’ve known for years in the holistic health community: That chemotherapy is, flatly stated, poison. It’s not “treatment,” it’s not medicine, and it’s not prevention or a cure. It’s poison with virtually no medicinal value except in perhaps one to two percent of cancer cases.

Aside from “Chemo brain” (a common term to describe the brain fog and memory loss that can happen after chemotherapy treatments for cancer), the No. 1 side effect of chemotherapy is, by the way, cancer. Cancer centers should technically be renamed “poison centers” because they are in the business of poisoning patients with a toxic cocktail of chemicals that modern science now reveals to be a cancer tumor growth accelerant!

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Comments

  1. This is one of the reasons why chemotherapies have been a dismal failure in cancer treatments. The future of successful cancer treatments are in the “targeted therapies” such as the “biologicals”, which include monoclonal antibodies, therapeutic cancer vaccines, oncolytic viruses, gene therapy & nanotechnology.

    Most physicians are completely unaware of the FDA approved cancer clinical research trials that are 20 years ahead of conventional medicine. Many of these cancer clinical research trials use “targeted therapies” that have very few side effects and focus on the cancer itself and not our healthy cells.

    It shows the ignorance of our judical & medical systems on this, when they try to jail parents of a child with cancer, when they refuse the death sentence of chemotherapy for their child. There are real alternatives right in our own medical schools, which are not allowed to advertise, because of the FDA, so very few physicians are aware of them.
    Look up these trials yourself at “clinicaltrials.gov” & take them to your physician to have him/her help you in understanding what they are targeting & how they work.
    Benjamin

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