S2 Subunit of SARS-nCoV-2 spike protein via In Silico Study (simulation) shows interaction with P53 tumor suppressor protein (Guardian of the genome) & BRCA (BRCA-1 & 2) suppressor protein; we can

thus extrapolate to the synthetic spike protein induced by mRNA technology gene injection; is this the reason for the surge in 'TURBO' cancers? surge in metastasis? relapses from cancer remission?

Is this the reason for the surge in 'TURBO' cancers? surge in metastasis? relapses from cancer remission? post COVID gene injection shot?

Some may argue that the in silico model is not as rigorous as comparative effectiveness trial research, even observational designs. Agreed but this is potent research and a serious red flag and we take it.

SOURCE:

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7324311/

p53 and BRCA are the well-known tumor suppressor proteins, that regulate downstream genes in response to numerous cellular stress and are frequently mutated in human cancer [5,6].

Interestingly we found p53, BRCA-1 and BRCA-2 interact with heptic repeat-2 region of S2 subunit through C- terminal domain.

PDB ID of these proteins was extracted from RCSB Protein Data Base (PDB) and details of crystal structure IDs and interacted amino acid residues are mentioned in the figure legend. This short bioinformatic analysis is a first time report and significant since COVID-19 is more fatal in people with underlying conditions specially lung diseases, diabetes and cancer. Therefore, further research is needed to understand COVID-19 effect in cancer patients and the detailed role of these interactions.’