4.7 Article

Reduced expression and growth inhibitory activity of the aging suppressor klotho in epithelial ovarian cancer

Journal

CANCER LETTERS
Volume 362, Issue 2, Pages 149-157

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2015.03.035

Keywords

Ovarian cancer; Klotho; Estrogen receptor; Tumor suppressor

Categories

Funding

  1. Israel Science Foundation (ISF) [1112/09]
  2. Israel Cancer Association Research Grant by Peter & Nancy Brown in memory of Eric Melvin Brown [20120047]
  3. Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
  4. American Cancer Society [RSG-10-252-01-TBG, SIOP-06-258-01-COUN]

Ask authors/readers for more resources

Klotho is an anti-aging transmembrane protein, which can be shed and function as a hormone. Accumulating data indicate klotho as a tumor suppressor in a wide array of malignancies, and we identified klotho as an inhibitor of the insulin-like growth factor (IGF-1) pathway in cancer cells. As this pathway is significant in the development of epithelial ovarian cancer (EOC) we studied klotho expression and activity in this tumor. Klotho mRNA levels were reduced in 16 of 19 EOC cell lines and immunohisto-chemistry analysis revealed high expression in normal ovaries, and reduced expression in 100 of 241 high grade papillary-serous adenocarcinoma of the ovaries, fallopian tubes and peritoneum. Reduced expression was associated with wild-type BRCA status. Klotho reduced EOC cell viability, enhanced cisplatin sensitivity, and reduced expression of mesenchymal markers. Finally, klotho inhibited IGF-1 pathway activation and inhibited transcriptional activity of the estrogen receptor. In conclusion, klotho is silenced in a substantial subset of the tumors and restoring its expression slows growth of EOC cells and inhibits major signaling pathways. As klotho is a hormone, treatment with klotho may serve as a novel treatment for EOC. (C) 2015 Elsevier Ireland Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available