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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.
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Journal ArticleDOI
MAP kinase and autophagy pathways cooperate to maintain RAS mutant cancer cell survival
Chih-Shia Lee,Liam C. Lee,Tina L. Yuan,Sirisha Chakka,Christof Fellmann,Scott W. Lowe,Scott W. Lowe,Scott W. Lowe,Natasha J. Caplen,Frank McCormick,Ji Luo +10 more
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.
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High-throughput screening with nucleosome substrate identifies small-molecule inhibitors of the human histone lysine methyltransferase NSD2.
Nathan P. Coussens,Stephen C. Kales,Mark J. Henderson,Olivia W. Lee,Kurumi Y. Horiuchi,Yuren Wang,Qing Chen,Ekaterina Kuznetsova,Jianghong Wu,Sirisha Chakka,Dorian M. Cheff,Ken Chih-Chien Cheng,Paul Shinn,Kyle R. Brimacombe,Min Shen,Anton Simeonov,Madhu Lal-Nag,Haiching Ma,Ajit Jadhav,Matthew D. Hall +19 more
TL;DR: It is found that all five N SD2 inhibitors bind the catalytic SET domain and one exhibited apparent activity in cells, validating the workflow and providing a template for identifying selective NSD2 inhibitors.
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Identification of novel molecular regulators of tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-induced apoptosis in breast cancer cells by RNAi screening
Sireesha V. Garimella,Kristie Gehlhaus,Jennifer L Dine,Jason J. Pitt,Magdalena Grandin,Sirisha Chakka,Marion M. Nau,Natasha J. Caplen,Stanley Lipkowitz +8 more
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.
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SLFN11 promotes CDT1 degradation by CUL4 in response to replicative DNA damage, while its absence leads to synthetic lethality with ATR/CHK1 inhibitors.
Ukhyun Jo,Yasuhisa Murai,Sirisha Chakka,Lu Chen,Ken Cheng,Junko Murai,Liton Kumar Saha,Lisa M. Miller Jenkins,Yves Pommier +8 more
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).
Georgios Pongas,Marianne K. Kim,Dong J. Min,Carrie D. House,Elizabeth Jordan,Natasha J. Caplen,Sirisha Chakka,Joyce C. Ohiri,Michael J. Kruhlak,Christina M. Annunziata +9 more
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.