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Working in mouse models, it was also shown that whilst mice lacking p21 were healthy, spontaneous tumours developed and G1 checkpoint control was compromised in cells derived from these mice. [27] [13] Taken together, these studies thus defined p21 as the primary mediator of p53-dependent cell cycle arrest in response to DNA damage.
The p53 upregulated modulator of apoptosis (PUMA) also known as Bcl-2-binding component 3 (BBC3), is a pro-apoptotic protein, member of the Bcl-2 protein family. [5] [6] In humans, the Bcl-2-binding component 3 protein is encoded by the BBC3 gene. [5] [6] The expression of PUMA is regulated by the tumor suppressor p53.
p53, also known as Tumor protein P53, cellular tumor antigen p53 (UniProt name), or transformation-related protein 53 (TRP53) is a regulatory protein that is often mutated in human cancers. The p53 proteins (originally thought to be, and often spoken of as, a single protein) are crucial in vertebrates , where they prevent cancer formation. [ 5 ]
Chk1/2 phosphorylate cdc25 which, in addition to being inhibited, is also sequestered in the cytoplasm by the 14-3-3 proteins. 14-3-3 are upregulated by p53, which, as previously mentioned, is activated by Chk1 and ATM/ATR. p53 also transactivates p21, and both p21 and the 14-3-3 in turn inhibit cyclin B-cdc2 complexes through the ...
[56] [57] Proteins p53, p21, p16ink4a, [58] and Bmi-1 have been termed as major senescence signalling factors, allowing them to serve as markers. [59] Other markers register morphology changes, reorganization of chromatin , apoptosis resistance, altered metabolism, enlarged cytoplasm or abnormal shape of the nucleus . [ 60 ]
p21 activated kinases (PAKs) are members of a family of enzymes. [1] They serve as targets for the small GTP binding proteins CDC42 and Rac and have been implicated in a wide range of biological activities. Members include: PAK1, regulating cell motility and morphology [2] PAK2, possibly playing a role in apoptosis [3]
The discovery of the first CKIs in yeast and P21 in mammals has led to research on family of molecules. [8] Further research has demonstrates that Cdks, cyclins and CKIs play essential roles in processes such as transcription , epigenetic regulation , metabolism , stem cell self-renewal, neuronal functions and spermatogenesis .
An important downstream target of ATM and ATR is p53, as it is required for inducing apoptosis following DNA damage. [60] The cyclin-dependent kinase inhibitor p21 is induced by both p53-dependent and p53-independent mechanisms and can arrest the cell cycle at the G1/S and G2/M checkpoints by deactivating cyclin/cyclin-dependent kinase ...