Differential gene expression identified in complete hydatidiform mole by combining suppression subtractive hybridization and cDNA microarray

被引:8
|
作者
Feng, HC
Tsao, SW
Ngan, HYS
Kwan, HS
Shih, SM
Xue, WC
Chiu, PM
Chan, KW
Cheung, ANY
机构
[1] Univ Hong Kong, Queen Mary Hosp, Dept Pathol, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, Queen Mary Hosp, Dept Anat, Hong Kong, Hong Kong, Peoples R China
[3] Univ Hong Kong, Queen Mary Hosp, Dept Obstet & Gynaecol, Hong Kong, Hong Kong, Peoples R China
[4] Univ Hong Kong, Queen Mary Hosp, Hong Kong Jockey Club Clin Res Ctr, Hong Kong, Hong Kong, Peoples R China
[5] Chinese Univ Hong Kong, Dept Biol, Hong Kong, Hong Kong, Peoples R China
关键词
differential gene expression; hydatidiform mole; suppression subtractive hybridization; cDNA microarray;
D O I
10.1016/j.placenta.2005.05.005
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Complete hydatidiform mole (CHM) is a type of gestational trophoblastic disease with pure paternal chromosome contribution and unpredictable malignant potential. As an attempt to assess the molecular pathogenesis of CHM, suppression subtractive hybridization (SSH) combined with cDNA microarray was used to compare the gene expression pattern of CHM compared with normal first-trimester placenta of similar gestational ages. cDNA microarray analysis using tissue-specific chips constructed with subtracted cDNA libraries identified 13 differentially expressed gene transcripts. Quantitative real-time polymerase chain reaction (PCR) confirmed up-regulation of human chorionic gonadotropin subunit (CGB) (P = 0.0008) and KIAA1200 (P = 0.0005), a G-protein regulator, as well as down-regulation of osteopontin (SPP1) (P < 0.0001) in 14 genotyped CHM when compared with 15 normal placentas. These candidate genes may contribute toward understanding the mechanism involved with the development and progression of CHM.
引用
收藏
页码:521 / 526
页数:6
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