alexa Side-population Cells Derived from Non-tumorigenic Rat Endometrial Cells are a Candidate Cell of Origin for Malignant Endometrial Tumors
ISSN: 2157-7633

Journal of Stem Cell Research & Therapy
Open Access

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Commentary

Side-population Cells Derived from Non-tumorigenic Rat Endometrial Cells are a Candidate Cell of Origin for Malignant Endometrial Tumors

Kiyoko Kato1*, Soshi Kusunoki1, Tetsunori Inagaki1, Nurisimangul Yusuf1, Hitomi Okabe1, Shin Suga1, Hiroshi Kaneda1, Yasuhisa Terao1, Takahiro Arima2, Kiyomi Tsukimori3 and Satoru Takeda1

1Department of Obstetrics and Gynecology, Faculty of Medicine, Juntendo University, Hongo 2-1-1, Bunkyo-ku, Tokyo, 113-8431, Japan

2Department of Informative Genetics, Environment and Genome Research Center, Tohoku University Graduate School of Medicine, 2-1 Seiryo-cho, Aoba-ku, Sendai, 980-8575, Japan

3Department of Obstetrics, Fukuoka Children’s Hospital, Tojinmachi 2-5-1, Chuo-ku, Fukuoka 810-0063, Fukuoka, Japan

*Corresponding Author:
Kiyoko Kato
Department of Obstetrics and Gynecology
Faculty of Medicine, Juntendo University
Hongo 2-1-1, Bunkyo-ku, Tokyo, 113-8431, Japan
Tel: 81-3-5802-1100
Fax: 81-3-5689-7460
E-mail: [email protected]

Received date: June 10, 2012; Accepted date: June 28, 2012; Published date: July 01, 2012

Citation: Kato K, Kusunoki S, Inagaki T, Yusuf N, Okabe H, et al. (2012) Sidepopulation Cells Derived from Non-tumorigenic Rat Endometrial Cells are a Candidate Cell of Origin for Malignant Endometrial Tumors. J Stem Cell Res Ther S7:003. doi:10.4172/2157-7633.S7-003

Copyright: © 2012 Kato K, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Abstract

We have previously demonstrated that side population (SP) cells derived from endometrial cancer cells have cancer stem-like cell features. However, the role of stem cell-enriched subpopulations, SP cells in normal endometrium for carcinogenesis is still poorly understood. In the present study, to modeled early carcinogenesis in normal endometrium, we established two cell lines by introducing the oncogenic KRAS gene into SP (RSP) cells and non-SP (RNSP) cells from a rat non-tumorigenic endometrial cell line. Tumorigenicity was enhanced in SP cells harboring mutant KRAS (RSP-K12V cells) compared with that in NSP harboring mutant KRAS gene (RNSP-K12V cells). The primary cultured tumor cells derived from RSP-K12V cells exhibited long-term proliferating capacity in culture and had the capacity to form serial tumors in vivo. In contrast, the primary cultured tumor cells derived from RNSP-K12V cells failed to grow and became senescent. The proportion of SP cells was higher in RSP-K12V cells than in RSP cells and was highest in the RSP-K12V tumor cells and it was correlated with tumorigenicity. The levels of c-Myc and Oct4, and the transcriptional activity of the estrogen receptor were enhanced in RSP-K12V cells and their tumor cells compared with those in RNSP-K12V cells and their tumor cells, respectively. Tumor cells derived RSP-K12V acquired the potential for estrogen-independent proliferation. This is the first report which demonstrates that the occurrence of KRAS gene mutations in SP cells rather than NSP cells derived from nontumorigenic endometrial cells, contributes to the development of malignant endometrial tumors.

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