Histotype-specific copy-number alterations in ovarian cancer

Ruby YunJu Huang, Geng Bo Chen, Noriomi Matsumura, Hung Cheng Lai, Seiichi Mori, Jingjing Li, Meng Kang Wong, Ikuo Konishi, Jean Paul Thiery, Liang K. Goh

Research output: Contribution to journalArticle

26 Citations (Scopus)

Abstract

Background: Epithelial ovarian cancer is characterized by multiple genomic alterations; most are passenger alterations which do not confer tumor growth. Like many cancers, it is a heterogeneous disease and can be broadly categorized into 4 main histotypes of clear cell, endometrioid, mucinous, and serous. To date, histotype-specific copy number alterations have been difficult to elucidate. The difficulty lies in having sufficient sample size in each histotype for statistical analyses. Methods: To dissect the heterogeneity of ovarian cancer and identify histotypes-specific alterations, we used an in silico hypothesis-driven approach on multiple datasets of epithelial ovarian cancer. Results: In concordance with previous studies on global copy number alterations landscape, the study showed similar alterations. However, when the landscape was de-convoluted into histotypes, distinct alterations were observed. We report here significant histotype-specific copy number alterations in ovarian cancer and showed that there is genomic diversity amongst the histotypes. 76 cancer genes were found to be significantly altered with several as potential copy number drivers, including ERBB2 in mucinous, and TPM3 in endometrioid histotypes. ERBB2 was found to have preferential alterations, where it was amplified in mucinous (28.6%) but deleted in serous tumors (15.1%). Validation of ERBB2 expression showed significant correlation with microarray data (p=0.007). There also appeared to be reciprocal relationship between KRAS mutation and copy number alterations. In mucinous tumors where KRAS mutation is common, the gene was not significantly altered. However, KRAS was significantly amplified in serous tumors where mutations are rare in high grade tumors. Conclusions: The study demonstrates that the copy number landscape is specific to the histotypes and identification of these alterations can pave the way for targeted drug therapy specific to the histotypes.

Original languageEnglish
Pages (from-to)47
Number of pages1
JournalBMC Medical Genomics
Volume5
DOIs
Publication statusAccepted/In press - Oct 18 2012
Externally publishedYes

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Ovarian Neoplasms
Neoplasms
Mutation
Neoplasm Genes
Computer Simulation
Sample Size
Drug Therapy
Growth
Genes
Ovarian epithelial cancer

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Huang, R. Y., Chen, G. B., Matsumura, N., Lai, H. C., Mori, S., Li, J., ... Goh, L. K. (Accepted/In press). Histotype-specific copy-number alterations in ovarian cancer. BMC Medical Genomics, 5, 47. https://doi.org/10.1186/1755-8794-5-47

Histotype-specific copy-number alterations in ovarian cancer. / Huang, Ruby YunJu; Chen, Geng Bo; Matsumura, Noriomi; Lai, Hung Cheng; Mori, Seiichi; Li, Jingjing; Wong, Meng Kang; Konishi, Ikuo; Thiery, Jean Paul; Goh, Liang K.

In: BMC Medical Genomics, Vol. 5, 18.10.2012, p. 47.

Research output: Contribution to journalArticle

Huang, RY, Chen, GB, Matsumura, N, Lai, HC, Mori, S, Li, J, Wong, MK, Konishi, I, Thiery, JP & Goh, LK 2012, 'Histotype-specific copy-number alterations in ovarian cancer', BMC Medical Genomics, vol. 5, pp. 47. https://doi.org/10.1186/1755-8794-5-47
Huang, Ruby YunJu ; Chen, Geng Bo ; Matsumura, Noriomi ; Lai, Hung Cheng ; Mori, Seiichi ; Li, Jingjing ; Wong, Meng Kang ; Konishi, Ikuo ; Thiery, Jean Paul ; Goh, Liang K. / Histotype-specific copy-number alterations in ovarian cancer. In: BMC Medical Genomics. 2012 ; Vol. 5. pp. 47.
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