Dual Function Research: The Spike Protein, Universal ACE2 Expression and the Quest to Create a Universal “Therapy” to Induce Cancer, Neurodegeneration and Fibrosis
ACE2 Gains a New Function when Interacting with the Spike Protein: It Becomes a LETHAL TRANSMITTER!
I nearly collapsed on my walk today when the implications of what you are about to read hit me. This is my most important work to date. I believe it is now possible to prove that the Spike Protein is a protein developed to have universal invasion and fatal pathological effects – ones that can easily be dismissed as “natural.” The only evidence we would see would be a dramatic rise in excess deaths due to cancer or fibrotic disease processes. And yes, we have that.
One of the major issues with gain-of-function research is that there are two sides to every coin. If you can develop a cure or treatment for a condition, the opposite effect can be discovered by studying the very same research. I believe this may be at the core of the Spike Protein of SARS-CoV-2.
What needs to be understood is that ACE2 is NOT, I repeat is NOT a transmembrane protein that is meant to signal within the cell. ACE2 is meant to cleave ANG II (overexpression of this is dangerous in and of itself) into ANG (1-7). However, something very interesting happens when the Spike Protein interacts with ACE2. ACE2 becomes a transmitter of CELL SIGNALING. In other words, it GIVES INSTRUCTIONS TO THE CELL. And, these instructions are BAD. VERY BAD. They tell the cell to upregulate cancer causing genes, downregulate cancer prevention genes and induce neurodegeneration and fibrosis.
Now, this is horrific enough, indeed. But what turns it into a nightmare beyond comprehension is that ACE2 is EVERYWHERE! It is in EVERY MAJOR ORGAN and the REPRODUCTIVE SYSTEM!
So, if you were to create a protein that could cause cancer and fibrotic disease, you would want it to be able to attach to something that was everywhere to cause maximum damage. This is war. Plain and simple. You wouldn’t want a protein that would just attach to certain cells, like liver cells or kidney cells, or CD4 T-Cells (as in the case of HIV). No. This protein attaches to cells in EVERY MAJOR ORGAN and the REPRODUCTIVE SYSTEM. And then it signals death.
Body Localization of ACE-2: On the Trail of the Keyhole of SARS-CoV-2
We now have ample evidence that the Spike Protein is indeed highly capable of and causing cancer and fibrotic disease:
The COVID-19 Cell Signalling Problem: Spike, RAGE, PKC, p38, NFκB & IL-6 Hyper-Expression and the Human Ezrin Peptide, VIP, PKA-CREB Solution
S2 subunit of SARS-nCoV-2 interacts with tumor suppressor protein p53 and BRCA: an in silico study
Mitogen Activated Protein Kinase (MAPK) Activation, p53, and Autophagy Inhibition Characterize the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Spike Protein Induced Neurotoxicity
The intersection of COVID-19 and cancer: signaling pathways and treatment implications
This possibility has actually been warned of before, but the authors of the study didn’t quite understand the big picture. Now we do.
SARS-CoV-2 Spike Protein Elicits Cell Signaling in Human Host Cells: Implications for Possible Consequences of COVID-19 Vaccines
I cannot emphasize this enough: SPIKE is the issue. REGARDLESS OF SOURCE. Reexposures or reinfections, it matters not. The effects appear to be cumulative. All I can say is direct production within the body should be more of a concern than the virus knocking at the door of our respiratory and digestive systems.
I would not be able to continue to work without your support. I will keep searching for ways to mitigate this devastating pathogen - which didn’t have to be here. Think about that. Given the recent findings by the Senate, NONE of this had to happen. NONE OF IT!
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