Proof That The Cancer Industry Doesn’t Want a Cure

“A safe and effective cure for cancer has been discovered with a drug that was once used for unusual metabolic problems. Yet, the cancer industry shows no interest with following up on dichloroacetate (DCA) research from University of Alberta in Edmonton, Canada, reported in 2007. That’s because DCA is no longer patented. (1)

That research also confirmed cancer as a metabolic malfunction, not a weird mutation of cells often explained away as a genetic issue. But the medical mafia doesn’t want you to hear about it. But it confirms what most alternative cancer therapists already know.

killing-cancer

Since Nixon declared the “war on cancer” in the 1970s, the cancer industry has succeeded with raising money for researching very expensive chemo substances at $50,000 to $100,000 per round or more for toxic therapies that rarely work. (2)

Chemo drugs usually lead to demanding more business with drugs to ease terrible side effects (http://www.naturalnews.com/034761_cancer_drugs_toxicity_Voraxaze.html). Meanwhile, more are getting cancer and more are dying from it, mostly because of the toxic treatments.

Explaining DCA research results Evangelos Michelakis and the Alberta University research team tested DCA on human cancer cells outside the body and in cancerous mice with profound success. DCA was once used for unusual metabolic disorders. The worst side effects, which rarely occur, include some numbness and an affected gait.

The mice were fed DCA in water, and in weeks they had remarkable tumor shrinkage. This indicates DCA can be taken orally. DCA works by restoring the cells’ mitochondria. Michelakis and his team had discovered that the mitochondria in cancer cells are not permanently damaged and irreparable. This is what mainstream medicine thinks. With mitochondria malfunctioning, cancer cells use glucose fermentation for survival energy. This fermentation occurs when glycolysis (glucose conversion) occurs in an anaerobic cellular environment, which can be created by benign tumor masses, toxins, and low pH levels. DCA restores mitochondria in cells to make them function properly. Another function of normal mitochondria is signaling apoptosis, or cellular self destruction. Normal cells die and become replaced constantly. But with cancer cells, the apoptosis signal is nullified, making cancer cells “immortal.” (3)

The Alberta University researchers also realized that glycolysis fermentation in cancer cells produces lactic acid. The lactic acid breaks down the collagen holding those cells together in a tumor. This allows cancer cells to easily break away from a tumor shrinking with mainstream therapies. The researchers reasoned this is why cancer metastasizes or spreads to different parts of the body or reappears after remission from chemo. Tragic hypocrisy Alternative cancer therapies have little or no problem with metastatic cancer or even cancer reoccurring after remission. Most alternative cancers simply cure cancers completely. DCA offers the cancer industry an opportunity to come up with a pharmaceutical cure that is much cheaper and safer than their current standard of care. Yet the cancer industry is ignoring this opportunity. Instead, DCA is a homeless orphan begging for research funds to avoid legal issues with off label use on cancer. (4)”.

“Alternative cancer practitioners have always simply tried out and when they succeeded shared them with others who cared more about healing than money and power.

The medical mafia has created a matrix that demands big bucks to make big bucks for sick care instead of curing. Everyone in on the scam makes out financially. The cancer industry accuses alternative cancer therapists of quackery and taking advantage of the desperately ill for financial gain. Accusing others of your motives and crimes is called projection.

The medical/pharmaceutical complex is crony capitalism that doesn’t want a cure for cancer from anywhere.

Sources for this article include: http://www.naturalnews.com

(1)http://www.newscientist.com/article/dn10971

(2)http://www.sawilsons.com/gonzalez2.htm

(3)http://www.cell.com/cancer-cell/retrieve/pii/S1535610806003722

(4)http://www.dca.med.ualberta.ca/Home/Donations/

(5)http://www.khanacademy.org/video/glycolysis?playlist=Biology”

Brazilian Wasp Venom Kills Cancer Cells, But Not Healthy Cells

“Wasps get their fair share of bad press. They have painful stingers, and they’re not as useful (or cute) to us as bees. However, their time to step in the spotlight may be just around the corner: Their venom has been shown to attack cancer cells while leaving healthy cells alone.

The cancer-targeting toxin in the wasp is called MP1 (Polybia-MP1) and until now, how it selectively eliminates cancer cells was unknown. According to new research, it exploits the atypical arrangement of fats, or lipids, in cancer cell membranes. Their abnormal distribution creates weak points where the toxin can interact with the lipids, which ultimately pokes gaping holes in the membrane. These are sufficiently large for essential molecules to start leaking out, like proteins, which the cell cannot function without.

The wasp responsible for producing this toxin is the Polybia paulista. The toxin has so far been tested on model membranes and examined using a broad range of imaging techniques. You can see the team’s research results in the Biophysical Journal.

The wasp, Polybia paulista, which produces the venom containing MP1. Professor Mario Palma/Sao Paulo State University.

“Cancer therapies that attack the lipid composition of the cell membrane would be an entirely new class of anticancer drugs,” said Paul Beales from the University of Leeds and co-author of the study. “This could be useful in developing new combination therapies, where multiple drugs are used simultaneously to treat a cancer by attacking different parts of the cancer cells at the same time.”

In healthy cell membranes, the inner layer (facing the inside of the cell) is packed with phospholipids, including PS (phosphatidylserine) and PE (phosphatidylethanolamine). However, in cancer cells, PS and PE are located on the outer layer of the cell membrane, facing the opposite way.

To test the different effects of PS and PE’s presence on a cell, the scientists examined how the MP1 interacted with model membranes infused with PE and/or PS. The presence of each phospholipid had a destructive effect on the cells. PS increased the chance of MP1 binding to the membrane by a factor of seven to eight. The presence of PE inflated the size of the holes created by the MP1 by a factor 20 to 30.

“Formed in only seconds, these large pores are big enough to allow critical molecules such as RNA and proteins to easily escape cells,” said João Ruggiero Neto from São Paulo State University and co-author of the study.

“The dramatic enhancement of the permeabilization induced by the peptide in the presence of PE and the dimensions of the pores in these membranes was surprising.”

The next stage for this research is to adjust the amino acid sequence of MP1 to see what gives it its selective properties, and to try and refine them.

“Understanding the mechanism of action of this peptide will help in translational studies to further assess the potential for this peptide to be used in medicine,” Beales says.

“As it has been shown to be selective to cancer cells and non-toxic to normal cells in the lab, this peptide has the potential to be safe, but further work would be required to prove that.” ( via iflscience.com )” copied.