Resveratrol Enhances Chemosensitivity in Mouse Melanoma Model Through Connexin 43 Upregulation

Environmental Toxicology

Volumn 30, Issue 8, 2015, Pages 877-886

  Cheng, Yu Jung ^a   Chang, Meng Ya ^b,c   Chang, Wen Wei ^d,e   Wang, Wei Kuang ^f   Liu, Chi Fan ^g   Lin, Song Tao ^g   Lee, Che Hsin ^g  

^a CHINA MEDICAL UNIVERSITY   (Taiwan)

^b TZU CHI UNIVERSITY   (Taiwan)

^c BUDDHIST TZU CHI GENERAL HOSPITAL   (Taiwan)

^d CHUNG SHAN MEDICAL UNIVERSITY   (Taiwan)

^e CHUNG SHAN MEDICAL UNIVERSITY HOSPITAL   (Taiwan)

^f FENG CHIA UNIVERSITY   (Taiwan)

^g CHINA MEDICAL UNIVERSITY   (Taiwan)

Author keywords

cisplatin; connexin 43; gap junctions; resveratrol

Indexed keywords

CELL DEATH; CHEMOTHERAPY; PROTEINS; TUMORS;

ANTI-TUMOR ACTIVITIES; CIS-PLATIN; COMBINATION THERAPY; CONNEXIN 43; GAP JUNCTION INTERCELLULAR COMMUNICATIONS; GAP JUNCTIONS; MITOGEN ACTIVATED PROTEIN KINASE; THERAPEUTIC EFFECTS;

RESVERATROL;

CISPLATIN; CONNEXIN 43; MITOGEN ACTIVATED PROTEIN KINASE; RESVERATROL; ANTINEOPLASTIC AGENT; GJA1 PROTEIN, MOUSE; STILBENE DERIVATIVE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANTINEOPLASTIC ACTIVITY; ARTICLE; B16-F10 CELL LINE; CANCER COMBINATION CHEMOTHERAPY; CELL COMMUNICATION; CELL PROLIFERATION; CELL VIABILITY; CHEMOSENSITIVITY; CONTROLLED STUDY; DRUG MECHANISM; GAP JUNCTION; MALE; MAPK SIGNALING; MELANOMA; MELANOMA CELL; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEPLETION; PROTEIN EXPRESSION; TUMOR VOLUME; UPREGULATION; ANIMAL; BIOSYNTHESIS; C57BL MOUSE; CELL DEATH; DOSE RESPONSE; DRUG EFFECTS; GENETICS; MELANOMA, EXPERIMENTAL; METABOLISM; SIGNAL TRANSDUCTION; TUMOR CELL LINE;

ANIMALS; ANTINEOPLASTIC AGENTS; ANTINEOPLASTIC AGENTS, PHYTOGENIC; CELL DEATH; CELL LINE, TUMOR; CISPLATIN; CONNEXIN 43; DOSE-RESPONSE RELATIONSHIP, DRUG; GAP JUNCTIONS; MALE; MELANOMA, EXPERIMENTAL; MICE; MICE, INBRED C57BL; MITOGEN-ACTIVATED PROTEIN KINASES; SIGNAL TRANSDUCTION; STILBENES; UP-REGULATION;

EID: 85027940704     PISSN: 15204081     EISSN: 15227278     Source Type: Journal    
DOI: 10.1002/tox.21952     Document Type: Article

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