The TP53 gene, encoding the P53 protein which is the GUARDIAN of the geneome, has a potent role in tumour-suppressing activity in the cellular response to stress; majority of the human cancer cells

exhibit inactivation of P53 pathway; along with inactivation of P53 guardian of the geneome tumor suppressor protein & toll-like (TL)receptors 7 & 8; does the mRNA technology jab subvert P53, TL 7& 8?

I find this paper to be very information on the P53 pathway and the role in cancer and thus the potentially devastating role of the mRNA technology injections on P53 and TL receptors 7 & 8 based on the TURBO cancers we are witnessing; what do you think?

SOURCE:

https://jmhg.springeropen.com/articles/10.1186/s43042-020-00089-x

‘Cells have evolved balanced mechanisms to protect themselves by initiating a specific response to a variety of stress. The TP53 gene, encoding P53 protein, is one of the many widely studied genes in human cells owing to its multifaceted functions and complex dynamics. The tumour-suppressing activity of P53 plays a principal role in the cellular response to stress. The majority of the human cancer cells exhibit the inactivation of the P53 pathway. In this review, we discuss the recent advancements in P53 research with particular focus on the role of P53 in DNA damage responses, apoptosis, autophagy, and cellular metabolism. We also discussed important P53-reactivation strategies that can play a crucial role in cancer therapy and the role of P53 in various diseases.’

‘In response to a variety of cellular stress such as genotoxic stress, ischemic stress, oncogenic expression, P53 acts as a sensor, and suppresses tumour development by promoting cell death or permanent inhibition of cell proliferation. It controls several genes that play a role in the arrest of the cell cycle, cellular senescence, DNA repair system, and apoptosis. P53 plays a crucial role in supporting DNA repair by arresting the cell cycle to purchase time for the repair system to restore genome stability. Apoptosis is essential for maintaining tissue homeostasis and tumour suppression. P53 can induce apoptosis in a genetically unstable cell by interacting with many pro-apoptotic and anti-apoptotic factors.

Furthermore, P53 can activate autophagy, which also plays a role in tumour suppression. P53 also regulates many metabolic pathways of glucose, lipid, and amino acid metabolism. Thus under mild metabolic stress, P53 contributes to the cell’s ability to adapt to and survive the stress.’