BNIP3 is essential for mediating 6-thioguanine- and 5-fluorouracil-induced autophagy following DNA mismatch repair processing

Cell Research

Volumn 20, Issue 6, 2010, Pages 665-675

  Zeng, Xuehuo ^a,b   Kinsella, Timothy J ^a,b  

^a Department of Radiation Oncology ^*  (United States)

^b CASE WESTERN RESERVE UNIVERSITY   (United States)

Author keywords

Autophagy; BNIP3; MTOR; Nucleoside analogs; P53

Indexed keywords

ANTINEOPLASTIC ANTIMETABOLITE; BNIP3 PROTEIN, HUMAN; FLUOROURACIL; MAMMALIAN TARGET OF RAPAMYCIN; MEMBRANE PROTEIN; ONCOPROTEIN; PROTEIN BAD; PROTEIN P53; TIOGUANINE;

APOPTOSIS; ARTICLE; AUTOPHAGY; CELL STRAIN HCT116; DNA DAMAGE; DRUG EFFECT; GENETICS; HUMAN; METABOLISM; MISMATCH REPAIR;

ANTIMETABOLITES, ANTINEOPLASTIC; APOPTOSIS; AUTOPHAGY; BCL-ASSOCIATED DEATH PROTEIN; DNA DAMAGE; DNA MISMATCH REPAIR; FLUOROURACIL; HCT116 CELLS; HUMANS; MEMBRANE PROTEINS; PROTO-ONCOGENE PROTEINS; THIOGUANINE; TOR SERINE-THREONINE KINASES; TUMOR SUPPRESSOR PROTEIN P53;

ADENOVIRIDAE;

EID: 77953286298     PISSN: 10010602     EISSN: 17487838     Source Type: Journal    
DOI: 10.1038/cr.2010.40     Document Type: Article

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