Open AccessGene expression pattern in apoptotic QGY‐7703 cells induced by homoharringtonine 1
Author(s) -
JIN Wei,
QU Lefeng,
CHEN Qin,
CHANG Xinzhong,
WU Jiong,
SHAO Zhimin
Publication year - 2007
Publication title -
acta pharmacologica sinica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.514
H-Index - 90
eISSN - 1745-7254
pISSN - 1671-4083
DOI - 10.1111/j.1745-7254.2007.00569.x
Subject(s) - homoharringtonine , apoptosis , gene , dna microarray , dna fragmentation , microbiology and biotechnology , biology , gene expression , complementary dna , microarray analysis techniques , cancer research , genetics , programmed cell death , myeloid leukemia
Aim: To classify the genes responsible for apoptosis in QGY‐7703 cells induced by homoharringtonine (HHT). Methods: Apoptosis in QGY‐7703 cells induced by HHT was demonstrated by DNA fragmentation and morphological observation. cDNA microarray technology was used to detect gene transcription, and the result of microarrays for genes was confirmed by RT‐PCR. Results: Seventy‐eight individual mRNA were identified and their transcription levels changed significantly. Those genes, of which 68% were upregulated and 32% were downregulated, were partially related to apoptosis. They were mostly oncogenes, tumor suppressors, enzymes, and kinases. Conclusion: HHT is a potential drug in the treatment of liver cancer. TGF‐β, TNF, FAS, p38 MAP K, and p53 apoptosis signaling pathways were activated during apoptosis in QGY‐7703 cells. Such inducible genes may play important roles in apoptosis and deserve to be further studied.