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PMID: 16144934 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, P.H.S.

Gene expression profiles associated with response to chemotherapy in epithelial ovarian cancers.

Jazaeri AA, Awtrey CS, Chandramouli GV, Chuang YE, Khan J, Sotiriou C, Aprelikova O, Yee CJ, Zorn KK, Birrer MJ, Barrett JC, Boyd J

Abstract

The goal of this study was to determine whether distinct gene expression profiles are associated with intrinsic and/or acquired chemoresistance in epithelial ovarian carcinoma. Gene expression profiles were generated from 21 primary chemosensitive tumors and 24 primary chemo-resistant tumors using cDNA-based microarrays. Gene expression profiles of both groups of primary tumors were then compared with those of 15 ovarian carcinomas obtained following platinum-based chemotherapy ("post-chemotherapy" tumors). A theme discovery tool was used to identify functional categories of genes involved in drug resistance. Comparison of primary chemosensitive and chemo-resistant tumors revealed differential expression of 85 genes (P < 0.001). Comparison of gene expression profiles of primary chemosensitive tumors and post-chemotherapy tumors revealed more robust differences with 760 genes differentiating the two groups (P < 0.001). In contrast, only 230 genes were differentially expressed between primary chemo-resistant and post-chemotherapy groups (P < 0.001). Common to both gene lists were 178 genes representing transcripts differentially expressed between post-chemotherapy tumors and all primary tumors irrespective of intrinsic chemosensitivity. The gene expression profile of post-chemotherapy tumors compared with that of primary tumors revealed statistically significant overrepresentation of genes encoding extracellular matrix-related proteins. These data show that gene expression profiling can discriminate primary chemo-resistant from primary chemosensitive ovarian cancers. Gene expression profiles were also identified that correlate with states of intrinsic and acquired chemoresistance and that represent targets for future investigation and potential therapeutic interventions.

MeSH Terms
Adult Aged Aged, 80 and over Antineoplastic Agents/therapeutic use Biomarkers, Tumor/genetics Carcinoma, Endometrioid/drug therapy,genetics Cystadenocarcinoma, Serous/drug therapy,genetics Female Gene Expression Profiling Gene Expression Regulation, Neoplastic Humans Immunoenzyme Techniques Middle Aged Neoplasm Proteins/genetics Neoplasm Staging Oligonucleotide Array Sequence Analysis Ovarian Neoplasms/drug therapy,genetics RNA, Neoplasm/genetics,metabolism Reverse Transcriptase Polymerase Chain Reaction
Chemicals
Antineoplastic Agents Biomarkers, Tumor Neoplasm Proteins RNA, Neoplasm
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Jazaeri Amir A
Laboratory of Biosystems and Cancer, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA.
Awtrey Christopher S
Chandramouli Gadisetti V R
Chuang Yao Eric
Khan Javed
Sotiriou Christos
Aprelikova Olga
Yee Cindy J
Zorn Kristin K
Birrer Michael J
Barrett J Carl
Boyd Jeff
Article Info
Journal
Clinical cancer research : an official journal of the American Association for Cancer Research
Abbr.
Clin Cancer Res
ISSN
1078-0432
Published
2005-09-01
Pages
6300-10
Language
English
Region
United States
NLM ID
9502500
Subset
IM
Grants
NCI NIH HHS · U01 CA88175 · United States
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