Sunday 2 June 2024

 

Spike of SARS-COV-2 BIOWEAPON Promotes CANCER. As the Vaccines One!


VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel

$ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts
Source: Embassy of Israel, Washington, D.C. and US Department of State.

by Fabio Giuseppe Carlo Carisio

VERSIONE IN ITALIANO

«The suppressive effect of SARS-CoV-2 spike on p53-dependent gene activation provides a potential molecular mechanism by which SARS-CoV-2 infection may impact tumorigenesis, tumor progression and chemotherapy sensitivity. In fact, cisplatin-treated tumor cells expressing spike S2 were found to have increased cell viability as compared to control cells. Further observations on γ-H2AX expression in spike S2-expressing cells treated with cisplatin may indicate altered DNA damage sensing in the DNA damage response pathway. The preliminary observations reported here warrant further studies to unravel the impact of SARS-CoV-2 and its various encoded proteins including spike on pathways of tumorigenesis and response to cancer therapeutics».

This is the Abstract of a study by ShengliangZhang (Laboratory of Translational Oncology and Experimental Cancer Therapeutics, Warren Alpert Medical School, Brown University, Providence, Rhode Island, USA) and Wafik S.El-Deiry just published in pre-print onBioRxiv (link in the sources) that has discovered yet another component related to SARS-Cov-2 that can promote cancer. 

The Brown University researchers’ finding is important both for the things it says — that spike subunits can promote cancer survival and growth by blocking a cancer suppressor gene known as p53 (below details) — but also for the things it doesn’t say.

SARS-COV-2 Manipulated in the Laboratory to Test an AIDS Vaccine

In fact, the study was not at all interested in the artificial origin of the COVID-19 virus which was constructed in the laboratory with multiple manipulations and enhancements of the viral load such as to increase the toxicity of the Spike protein, already dangerous in itself for humans.

In fact, HIV sequences were inserted into it which induced professors Luc Montagnier, late biologist, Jean-Claude Perez, biomathematician co-signatory of the research on the artificial origin of SARS-Cov-2 censored for over a year by the scientific community, Pierre Bricage , molecular and biological engineer and former NATO consultant on bacteriological weapons, and finally Joseph Mercola, naturopathic doctor, believed that the AIDS pathogen had been inserted specifically to test the reactions of the world population to a possible vaccine against HIV (promptly developed by Moderna and in the clinical trials phase).

Toxic Protein and Other Ingredients of Cancer-Causing mRNA Serum Genes

On the basis of a similar analysis, it can therefore be hypothesized that SARS-COV-2 was deliberately altered, in its Omicron variant which is less lethal in the short term and with enormous genetic differences from the first Wuhan strain, precisely to experiment on unpaid human guinea pigs the effects of a virus and the resulting vaccines in order to achieve the great mirage of medical science of producing an mRNA genetic serum against cancer.

It is known that Big Pharma is financed by military agencies such as the Pentagon’s DARPA which therefore not only want to develop new bacteriological weapons but also find countermeasures to them, already experimenting with those on which the enemy could be working but which are not yet known.

The agreement between the USA and China signed already in 1998 by presidents Bill Clinton and Jiang Zemin, the obsession of the Obama-Biden administration with coronaviruses (and with the biomedical use of graphene) andexperiments on other pathogens in Georgia and Ukraine, such as the very recent work of some Chinese military doctors who created a prototype of SARS that can be defined as version 3 for 100% lethality.

The business started by Big Pharma on Covid vaccines has proven to be dangerous due to its potential tumor consequences both due to the toxic and inflammatory nanoparticles, both for the diabolical molecule N1-Methylpseudouridine, and for the Spike DNA fragments persistent in the human body, and for the inclusion of the simian vacuolizing virus, abbreviated SV40, whose presence Pfizer has not declared in its Comirnaty vaccineproduced with Biontech.

Before the same Pfizer deciding to invest billions of dollars in the purchase of a pharmaceutical company specialized in vaccines against tumors which have already been tested on an Australian doctor who fell ill with turbo-cancer after the mRNA genetic serum.

Fabio Giuseppe Carlo Carisio
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COVID Spike Proteins Help Cancer Cells Survive, Resist Chemotherapy: Brown University Preprint Paper

by Marina Zhang – originally published by The Epoch Times

All links to previous Gospa News articles have been added aftermaths, for to ties to the topics highlighted

Spike protein from SARS-CoV-2, the virus that causes COVID-19, potentially promotes cancer by interfering with anti-cancer activities, according to a recent preprint cell study from Brown University.

The preprint authors, led by Dr. Wafik El-Deiry, director of the Cancer Center at Brown University, exposed cancer cells to spike protein subunits. They found that the spike subunits may promote cancer survival and growth by blocking a cancer suppressor gene known as p53.

The gene—the most commonly affected by cancer—stops cancer cell growth and encourages DNA repair. “Interfering with p53 can promote cancer development as well as aid cancer growth,” Dr. El-Deiry told The Epoch Times.

When exposed to chemotherapy, cancer cells containing spike protein subunits had a better chance of survival.

“We saw enhanced cancer cell viability in the presence of SARS-CoV-2 spike S2 subunit after treatment with several chemotherapy agents,” said Dr. El-Deiry.

Spike Subunits Block Anti-Cancer Gene

The SARS-CoV-2 spike protein comprises two components: S1 and S2. In this study, the researchers tested the effects of the S2 component in several human cancer cell lines: lung, breast, colorectal, and sarcoma cancer cells.

All cells were modified to include normal p53 genes, and some were introduced to spike protein S2 DNA. The researchers then used chemotherapy drugs to activate the p53 genes and cause cancer cell death.

However, they found that cancer cells with spike protein S2 tended to survive the effects of the anti-cancer gene and chemotherapy. They also observed that p53 activity was reduced in these cells.

It is still unknown why cancer cells with spike protein S2 DNA had better survival rates. Dr. El-Deiry said it could be because S2 proteins seem to interfere with p53 activity. However, S2 proteins may also cause “other effects that promote cell survival” even in the presence of toxic chemotherapy.

COVID-19 Vaccines May Have Similar Effects

Dr. El-Deiry’s study was designed to test whether the SARS-CoV-2 virus or its viral subunits could promote cancer activities.

However, the study further implied that SARS-CoV-2 therapeutics like the COVID-19 mRNA and protein vaccines may yield similar effects.

“Our goal was to study spike protein regardless of its origin,” Dr. El-Deiry told The Epoch Times. “We focused on spike that may come from infection or any other way it can be expressed in human cells … this would also apply to vaccine-made spike.”

Dr. El-Deiry was careful to highlight the many limitations of his study, including that it was a simple cell culture study. Additionally, with differing spike variations in the different viral strains and vaccines, the health consequences they may have require more research.

More Thorough Studies Needed

When asked if human cancers carry the same risks when exposed to spike protein S2, Dr. El-Deiry said their current data are too preliminary to know.

He said additional animal studies would be needed to “more thoroughly [evaluate] cancer susceptibility.”

He would also like to examine the behaviors of normal cell types and their responses to different spike variants.He hopes that the spike proteins generated by future vaccines will not suppress p53 activity.

Dr. El-Deiry added that questions remain to be answered, such as whether these potential cancer-promoting effects are reversible, how long the spike proteins persist in the cells, and whether these risks can be mitigated.

“Some of the questions have relevance to long COVID as well as repeated administration of vaccines with stable RNA that introduces it into normal cells,” he said.

Several Studies Link Cancer to COVID-19 Pandemic

WHOLE ARTICLE CONTINUES HERE

by Marina Zhang – originally published by The Epoch Times


MAIN SOURCES

BIORXIV – SARS-CoV-2 spike S2 subunit inhibits p53 activation of p21(WAF1), TRAIL Death Receptor DR5 and MDM2 proteins in cancer cells

GOSPA NEWS – COVID-19 DOSSIER

GOSPA NEWS – WUHAN-GATES DOSSIER


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