Serial analysis of gene expression identifies connective tissue growth factor expression as a prognostic biomarker in gallbladder cancer

被引:33
作者
Alvarez, Hector [1 ,5 ]
Corvalan, Alejandro [5 ]
Roa, Juan C. [7 ]
Argani, Pedram [1 ]
Murillo, Francisco [4 ]
Edwards, Jennifer [2 ]
Beaty, Robert [1 ]
Feldmann, Georg [1 ]
Hong, Seung-Mo [1 ]
Mullendore, Michael [1 ]
Roa, Ivan [7 ]
Ibanez, Luis [6 ]
Pimente, Fernando [6 ]
Diaz, Alfonso [8 ]
Riggins, Gregory J. [2 ,3 ]
Maitra, Anirban [1 ,3 ,4 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurosurg, Baltimore, MD 21231 USA
[3] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21231 USA
[4] Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21231 USA
[5] Pontificia Univ Catolica Chile, Dept Pathol, Santiago, Chile
[6] Pontificia Univ Catolica Chile, Dept Surg, Santiago, Chile
[7] Univ La Frontera, Dept Pathol, Temuco, Chile
[8] Hosp Dr Sotero del Rio, Dept Surg, Santiago, Chile
关键词
D O I
10.1158/1078-0432.CCR-07-1991
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: Gallbladder cancer (GBC) is an uncommon neoplasm in the United States, but one with high mortality rates. This malignancy remains largely understudied at the molecular level such that few targeted therapies or predictive biomarkers exist. Experimental Design: We built the first series of serial analysis of gene expression (SAGE) libraries from GBC and nonneoplastic gallbladder mucosa, composed of 21-bp long-SAGE tags. SAGE libraries were generated from three stage-matched GBC patients (representing Hispanic/ Latino, Native American, and Caucasian ethnicities, respectively) and one histologically alithiasic gallbladder. Real-time quantitative PCR was done on microdissected epithelium from five matched GBC and corresponding nonneoplastic gallbladder mucosa. Immunohistochemical analysis was done on a panel of 182 archival GBC in high-throughput tissue microarray format. Results: SAGE tags corresponding to connective tissue growth factor (CTGF) transcripts were identified as differentially overexpressed in all pairwise comparisons of GBC (P < 0.001). Real-time quantitative PCR confirmed significant overexpression of CTGF transcripts in microdissected primary GBC (P < 0.05), but not in metastatic GBC, compared with nonneoplastic gallbladder epithelium. By immunohistochemistry, 66 of 182 (36%) GBC had high CTGF antigen labeling, which was significantly associated with better survival on univariate analysis (P = 0.0069, log-rank test). Conclusions: An unbiased analysis of the GBC transcriptome by SAGE has identified CTGF expression as a predictive biomarker of favorable prognosis in this malignancy. The SAGE libraries from GBC and nonneoplastic gallbladder mucosa are publicly available at the Cancer Genome Anatomy Project web site and should facilitate much needed research into this lethal neoplasm.
引用
收藏
页码:2631 / 2638
页数:8
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