scispace - formally typeset
S

Sirisha Chakka

Researcher at National Institutes of Health

Publications -  8
Citations -  260

Sirisha Chakka is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Cancer cell & mTORC2. The author has an hindex of 6, co-authored 8 publications receiving 170 citations.

Papers
More filters
Journal ArticleDOI

MAP kinase and autophagy pathways cooperate to maintain RAS mutant cancer cell survival

TL;DR: It is found that RAF node knockdown best differentiated KRAS mutant and KRAS WT cancer cells, suggesting RAF kinases are key oncoeffectors for KRAS addiction, and cotargeting the RAF, RAC, and autophagy pathways can improve the capture of KRAS dependency better than targeting RAF alone.
Journal ArticleDOI

Identification of novel molecular regulators of tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-induced apoptosis in breast cancer cells by RNAi screening

TL;DR: It is confirmed that small-molecule inhibition of SRC or BCL2L1, in combination with TRAIL, sensitizes breast cancer cells to TRAIL-induced apoptosis, including cell lines resistant to TRAil-induced cytotoxicity.
Journal ArticleDOI

SLFN11 promotes CDT1 degradation by CUL4 in response to replicative DNA damage, while its absence leads to synthetic lethality with ATR/CHK1 inhibitors.

TL;DR: In this paper, the authors performed an unbiased genome-wide RNAi screen in SLFN11-WT and -knockout (KO) cells and found that inactivation of Ataxia Telangiectasia- and Rad3-related (ATR), CHK1, BRCA2, and RPA1 overcome chemoresistance to camptothecin (CPT) in cancer cells.
Journal ArticleDOI

BRD4 facilitates DNA damage response and represses CBX5/Heterochromatin protein 1 (HP1).

TL;DR: The results provide a strong rationale for clinical investigation of CHK1 and BRD4 co-inhibition, especially for HGSOC patients withBRD4 overexpression, and increase the anti-tumor activity of this pathway.