Diallyl disulfide inhibits the proliferation of HT-29 human colon cancer cells by inducing differentially expressed genes

Molecular Medicine Reports

Volumn 4, Issue 3, 2011, Pages 553-559

  Huang, You Sheng ^a,b   Xie, Na ^a,b   Su, Qi ^a   Su, Jian ^a   Huang, Chen ^a   Liao, Qian Jin ^a  

^a UNIVERSITY OF SOUTH CHINA   (China)

^b HAINAN MEDICAL UNIVERSITY   (China)

Author keywords

Colon cancer; Diallyl disulfide; Gene expression; HT 29 cells; Suppression subtractive hybridization

Indexed keywords

3 (4,5 DIMETHYL 2 THIAZOLYL) 2,5 DIPHENYLTETRAZOLIUM BROMIDE; CALCYCLIN; CELL PROTEIN; CITRATE SYNTHASE; COMPLEMENTARY DNA; COPPER ZINC SUPEROXIDE DISMUTASE; DIALLYL DISULFIDE; G PROTEIN COUPLED RECEPTOR; G PROTEIN COUPLED RECEPTOR 175; GALECTIN 8; HEAT SHOCK PROTEIN 90; MESSENGER RNA; PROTEIN ANKRD39; PROTEIN ARPC3; PROTEIN DNCL1; PROTEIN FTH1; PROTEIN GNB1; PROTEIN HNRPAB; PROTEIN KRT80; PROTEIN MM1; PROTEIN P21; PROTEIN PABPC1; PROTEIN PSMD12; PROTEIN RPL35A; PROTEIN SPINT2; PROTEIN TACSTD2; PROTEIN UBA52; RAC1 PROTEIN; RIBOSOMAL PROTEIN S3; SCLEROPROTEIN; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; APOPTOSIS; ARTICLE; CANCER CELL; CANCER INHIBITION; CELL ASSAY; CELL CYCLE; CELL GROWTH; CELL METABOLISM; CELL PROLIFERATION; COLON CANCER; COLON CARCINOGENESIS; CONTROLLED STUDY; DNA LIBRARY; DOSE TIME EFFECT RELATION; DOWN REGULATION; DRUG CYTOTOXICITY; DRUG MECHANISM; FLOW CYTOMETRY; GENE EXPRESSION; GENETIC IDENTIFICATION; GENETIC SCREENING; GENETIC TRANSDUCTION; HUMAN; HUMAN CELL; MITOSIS INHIBITION; NUCLEOTIDE SEQUENCE; QUANTITATIVE ANALYSIS; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SUPPRESSION SUBTRACTIVE HYBRIDIZATION; UPREGULATION;

ALLYL COMPOUNDS; CELL CYCLE; CELL DEATH; CELL PROLIFERATION; COLONIC NEOPLASMS; DISULFIDES; DOWN-REGULATION; DRUG SCREENING ASSAYS, ANTITUMOR; FLOW CYTOMETRY; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION, NEOPLASTIC; HT29 CELLS; HUMANS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER; TIME FACTORS; UP-REGULATION;

ALLIUM SATIVUM; RODENTIA;

EID: 79953780994     PISSN: 17912997     EISSN: 17913004     Source Type: Journal    
DOI: 10.3892/mmr.2011.453     Document Type: Article

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