HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Suppression of REV7 enhances cisplatin sensitivity in ovarian clear cell carcinoma cells.

Abstract
Human REV7 (also known as MAD2L2 and MAD2B) is involved in DNA repair, cell cycle regulation, gene transcription, and carcinogenesis. In this study, we evaluated the expression of REV7 in epithelial ovarian cancer (EOC) and analyzed the association between its expression and chemosensitivity in ovarian clear cell carcinoma (CCC) cells. Expression of REV7 in human EOC tissues was assessed by immunohistochemical staining. Expression was detected in the majority of EOCs (92.0%) with especially high levels of expression frequently observed in CCCs (73.5%) compared with that of non-CCCs (53.4%). Enhanced immunoreactivity to REV7 was associated with poor prognosis represented by reduced progression-free survival in advanced stage (stage II-IV) EOC as assessed using Kaplan-Meier curves and log-rank tests. The effects of REV7 knockdown on cell proliferation and chemosensitivity in CCC cells were also analyzed in vitro and in vivo. Knockdown of REV7 in CCC cells decreased cell proliferation without affecting cell cycle distribution. Additionally, the number of apoptotic cells and DNA damaged cells were increased after cisplatin treatment. In a nude mouse tumor xenograft model, inoculated REV7-knockdown tumors showed significantly reduced tumor volumes after cisplatin treatment compared with those of the control group. These findings indicate that depletion of REV7 enhances sensitivity to cisplatin treatment in CCC, suggesting that REV7 is a candidate molecular target in CCC management.
AuthorsKaoru Niimi, Yoshiki Murakumo, Naoki Watanabe, Takuya Kato, Shinji Mii, Atsushi Enomoto, Masato Asai, Naoya Asai, Eiko Yamamoto, Hiroaki Kajiyama, Kiyosumi Shibata, Fumitaka Kikkawa, Masahide Takahashi
JournalCancer science (Cancer Sci) Vol. 105 Issue 5 Pg. 545-52 (May 2014) ISSN: 1349-7006 [Electronic] England
PMID24597627 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2014 The Authors. Cancer Science published by Wiley Publishing Asia Pty Ltd on behalf of Japanese Cancer Association.
Chemical References
  • Antineoplastic Agents
  • MAD2L2 protein, human
  • Mad2 Proteins
  • RNA, Small Interfering
  • Cisplatin
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • Antineoplastic Agents (pharmacology)
  • Apoptosis (genetics)
  • Carcinoma, Ovarian Epithelial
  • Cell Cycle (genetics)
  • Cell Proliferation
  • Cisplatin (pharmacology, therapeutic use)
  • DNA Repair (genetics)
  • Drug Resistance, Neoplasm (genetics)
  • Female
  • Humans
  • Mad2 Proteins (genetics)
  • Male
  • Mice
  • Mice, Nude
  • Middle Aged
  • Neoplasms, Glandular and Epithelial (drug therapy)
  • Ovarian Neoplasms (drug therapy)
  • RNA Interference
  • RNA, Small Interfering
  • Tumor Cells, Cultured
  • Xenograft Model Antitumor Assays
  • Young Adult

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: