Abstract/References

Differentiation of ovarian serous carcinoma from ovarian clear cell carcinoma using a 10-gene signature selected by comprehensive gene expression analysis

Shinji Nomura, Takafumi Watanabe, Reiko Honma, Susumu Matsukura, Emi Ito, Jun-ichi Imai, Yuichiro Kiko, Osamu Suzuki, Yuko Hashimoto, Manabu Kojima, Shigenori Furukawa, Shu Soeda, Shinya Watanabe, Keiya Fujimori

Author information
  • Shinji Nomura

    Department of Obstetrics and Gynecology, Fukushima Medical University

  • Takafumi Watanabe

    Department of Obstetrics and Gynecology, Fukushima Medical University

  • Reiko Honma

    Nippon Gene Co., Ltd.

  • Susumu Matsukura

    Medicrome Inc.

  • Emi Ito

    Translational Research Center, Fukushima Medical University

  • Jun-ichi Imai

    Translational Research Center, Fukushima Medical University

  • Yuichiro Kiko

    Department of Diagnostic Pathology, Fukushima Medical University

  • Osamu Suzuki

    Department of Diagnostic Pathology, Fukushima Medical University

  • Yuko Hashimoto

    Department of Diagnostic Pathology, Fukushima Medical University

  • Manabu Kojima

    Department of Obstetrics and Gynecology, Fukushima Medical University

  • Shigenori Furukawa

    Department of Obstetrics and Gynecology, Fukushima Medical University

  • Shu Soeda

    Department of Obstetrics and Gynecology, Fukushima Medical University

  • Shinya Watanabe

    Translational Research Center, Fukushima Medical University

  • Keiya Fujimori

    Department of Obstetrics and Gynecology, Fukushima Medical University

Abstract

Aim:Ovarian serous carcinoma (OSC) and ovarian clear cell carcinoma (OCCC) are two major histological types of epithelial ovarian carcinoma (EOC), each with different biological features and clinical behaviors. Although immunostaining is commonly used for differential diagnosis between OSC and OCCC, correct identification of EOC with mixed-type histology is sometimes a diagnostic challenge. The aim of the present study was to explore candidate genes as potential diagnostic biomarkers that distinguish OSC from OCCC.


Methods:A total of 57 surgical specimens were obtained from EOC patients who had previously undergone primary debulking surgery. Total RNAs were extracted from fresh-frozen tissues of EOC patients, and were used for comprehensive gene expression analysis using DNA microarray technology.


Results:Ten candidate genes, FXYD2, TMEM101, GABARAPL1, ARG2, GLRX, RBPMS, GDF15, PPP1R3B, TOB1, and GSTM3 were up-regulated in OCCC compared to OSC. All EOC patients were divided into two groups according to hierarchical clustering using a 10-gene signature.


Conclusion:Our data suggest that the 10 candidate genes would be an excellent marker for distinguishing OSC from OCCC. Furthermore, the molecular signatures of the 10 genes may enlighten us on the differences in carcinogenesis, and provide a theoretical basis for OCCC’s resistance to chemotherapy in the future.


The cintent of reseach paper

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