realize the potential of Metabolic Medicine
KGK Synergize
Lab Tests on Cell Lines
Oncology Outcome Studies
Oncologist 1,000 Patient/Stage IV Study
Published Articles
Poly-MVA / Lipoic Acid Complex articles on Pubmed.com
Poly-MVA Inventor Papers
Dr. Merrill Garnett
Metabolic Cancer Therapies


Oxidative energy production takes place in a cellular organelle called the mitochondria. The mitochondria are known as the cellular “power plants.” Also telling is the fact that the greater the degree of fermentation displayed by a given cancer, the more aggressive the cancer. Because a tumor cell’s mitochondria appear to be dis-regulated, and generate energy by such an inefficient pathway, they have to consume much more glucose to remain viable. A glance at a PET scan, which uses a radioactive labeled glucose analog to image cancer, provides stunning visual evidence of the voracious appetite tumor cells have for glucose compared to normal tissue.
Altered Metabolism May be One of the Drivers of Cancer
It is well established that once a cell has an impaired ability to produce energy through oxidative pathways, the genomic instability (increased potential for DNA mutations to occur) that accompanies tumor development, inevitable follows. While it’s true that most of the agents known to cause cancer; chemical carcinogens, viruses, radiation, and inflammation can cause mutations to DNA, it is also true these provocative agents damage the mitochondria. The metabolic theory of cancer states that once the mitochondria of a given cell become disregulated, and the cell reverts to fermentation to obtain energy, a plethora of metabolic and epigenetic modifications participate in the origin of cancer.
Poly-MVA Research, Science and Studies
Poly MVA Laboratory
Lung Cancer Study
Low Dose Chemo Report
Stage 4 Oncology Studies
Frank Antonowich PhD
READ REPORT
Published Scientific Study
READ REPORT
Oncology Study Overview
READ REPORT
James W. Forysythe, M.D. H.M.D.
READ REPORT
Poly-MVA Articles
Cancer Tutor
Naturopathic Medicine
Cancer-Stroke-Anti-Aging
Cancer-Stroke-Anti-Aging

In 2007, KGK Science, Inc., an independent laboratory in Canada, examined the effects of POLY-MVA on 8 cancer cell lines.
These lines included:
1) Skin melanoma, human (SKMel-5)
2) Liver, hepatocellular carcinoma, human (Hep G2)
3) Lung, malignant melanoma, human (Malme-3M)
4) Mammary gland, ductal carcinoma, human (MDA-MB 435)
5) Prostate, left supraclavicular lymph node carcinoma, human (LNCaP)
6) Colon, colorectal adenocarcinoma, human (HT-29)
7) Human brain, glioblastoma; astrocytoma (U87)
8) Glioblastoma (HT-80)
POLY-MVA was administered at 3 different dosages and the number of cells was examined after 24, 48 and 72 hours following initial application. POLY-MVA was effective, to varying degrees, on the entire group of cell lines tested (melanoma, liver, lung, breast, prostate, colon, astrocytoma and glioblastoma).
The varying effectiveness appears to be a consequence of the particular cell lines used and their associated degree of anaplasia.

The graph above demonstrates the benefit of POLY-MVA after 48 hours of initial exposure: The Y-axis represents the number of cells per mL.

Poly MVA causes significant cell death after 48 Hours of exposure
per mL. SHAPE \* MERGEFORMAT CPM
The table below illustrates the statistically significant level of cell death
(p must be equal to or less than 0.05) induced by POLY-MVA after 48 hours of initial exposure:
Garnett McKeen In vitro Cancer Assays:
Garnett McKeen Laboratory Inc. (GML) chose to mimic the National Cancer Institute’s (NCI) cell screening protocol.
The following cell lines were selected from the NCI repository:
MCF-7 (breast adenocarcinoma), and A549 (lung non-small cell adenocarcinoma).
The data below represents the completion of the Breast Cancer (MCF-7), Ovarian Cancer (OVCAR-5) and Lung Carcinoma (A549) assay.
We have also completed assays using stage IV glioblastoma multiforme (H-80) and astrocytoma (H-4) brain tumor lines.
As noted below, all of the studies demonstrated significant cell death.

CANCER CELL DEATH RATE IN 5 CELL LINES
After 48 hours of exposure




