Both ERK1 and ERK2 kinases promote G2/M arrest in etoposide-treated MCF7 cells by facilitating ATM activation

Cellular Signalling

Volumn 22, Issue 11, 2010, Pages 1783-1789

  Wei, Fengxiang ^a,b,c   Xie, Yanyun ^a,b,d   Tao, Lijian ^d   Tang, Damu ^a,b  

^a MCMASTER UNIVERSITY   (Canada)

^b ST JOSEPH S HOSPITAL   (Canada)

^c GUANGDONG PHARMACEUTICAL UNIVERSITY   (China)

^d CENTRAL SOUTH UNIVERSITY   (China)

Author keywords

ATM; CDC25C; CHK2; DNA damage response (DDR); ERK1 2 kinases; G2 M arrest

Indexed keywords

ATM PROTEIN; CHECKPOINT KINASE 2; ETOPOSIDE; MITOGEN ACTIVATED PROTEIN KINASE 1; MITOGEN ACTIVATED PROTEIN KINASE 3; PROTEIN TYROSINE PHOSPHATASE; SERINE; SMALL INTERFERING RNA; THREONINE;

ARTICLE; CELL CYCLE ARREST; CELL CYCLE G2 PHASE; CELL CYCLE M PHASE; CELL STRAIN MCF 7; CONTROLLED STUDY; DNA DAMAGE; ENZYME ACTIVATION; ENZYME PHOSPHORYLATION; ENZYME SUBSTRATE; PRIORITY JOURNAL;

CDC25 PHOSPHATASES; CELL CYCLE PROTEINS; CELL DIVISION; CELL LINE, TUMOR; DNA DAMAGE; DNA-BINDING PROTEINS; ETOPOSIDE; G2 PHASE; HISTONES; HUMANS; MITOGEN-ACTIVATED PROTEIN KINASE 1; MITOGEN-ACTIVATED PROTEIN KINASE 3; PHOSPHORYLATION; PROTEIN-SERINE-THREONINE KINASES; RNA INTERFERENCE; RNA, SMALL INTERFERING; TUMOR SUPPRESSOR PROTEINS;

ATAXIA TELANGIECTASIA;

EID: 77955655466     PISSN: 08986568     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cellsig.2010.07.007     Document Type: Article

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