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Prognostic impact of the cancer stem cell-related marker NANOG in ovarian serous carcinoma.

Authors
 Lee, Maria  ;  Nam, Eun Ji  ;  Kim, Sang Wun  ;  Kim, Sunghoon  ;  Kim, Jae Hoon  ;  Kim, Young Tae 
Citation
 INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, Vol.22(9) : 1489-1496, 2012 
Journal Title
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER
ISSN
 1048-891X 
Issue Date
2012
MeSH
Adult ; Aged ; Antineoplastic Agents/therapeutic use ; Biomarkers, Tumor/genetics ; Biomarkers, Tumor/metabolism ; Biomarkers, Tumor/physiology ; Cell Line, Tumor ; Cystadenocarcinoma, Serous/diagnosis* ; Cystadenocarcinoma, Serous/genetics ; Cystadenocarcinoma, Serous/mortality ; Cystadenocarcinoma, Serous/pathology ; Drug Resistance, Neoplasm/drug effects ; Drug Resistance, Neoplasm/genetics ; Female ; Gene Expression Regulation, Neoplastic/physiology ; Homeodomain Proteins/genetics* ; Homeodomain Proteins/metabolism ; Homeodomain Proteins/physiology ; Humans ; Middle Aged ; Nanog Homeobox Protein ; Neoplastic Stem Cells/metabolism* ; Neoplastic Stem Cells/pathology ; Ovarian Neoplasms/diagnosis* ; Ovarian Neoplasms/genetics ; Ovarian Neoplasms/mortality ; Ovarian Neoplasms/pathology ; Paclitaxel/therapeutic use ; Prognosis ; Survival Analysis ; Young Adult
Keywords
NANOG ; Cancer stem cell ; Ovarian cancer ; Chemoresistance ; Prognosis
Abstract
OBJECTIVE: The objective of this study was to evaluate the prognostic significance of NANOG expression in ovarian serous carcinoma.

METHODS: The expression of NANOG was evaluated in 6 ovarian carcinoma cell lines, paclitaxel-resistant SKOV3 cells, and SKOV3 spheroid cells with semiquantitative reverse transcription-polymerase chain reaction and Western blotting. NANOG expression was also measured immunohistochemically in a tissue microarray containing ovarian tissues from 74 patients with ovarian serous carcinoma and 24 with ovarian serous cystadenoma. Each sample was scored based on signal intensity and proportion, and a score greater than 4 was considered "positive."

RESULTS: NANOG mRNA expression was variable in different ovarian cancer cell lines. The mRNA level of NANOG was increased in the paclitaxel-resistant SKOV3 cells and SKOV3 spheroid cells compared with that in the SKOV3 cells. NANOG expression was positive in 21.6% of 74 ovarian serous carcinoma tissues, but none of the ovarian serous cystadenoma tissues were positive. Positive NANOG expression was associated with residual tumor size after surgery (P = 0.032). The overall survival of the patients with positive NANOG expression was poorer than that of the patients with negative NANOG expression (P = 0.020). In patients with stage I and II disease, positive NANOG expression was independently associated with shorter overall survival compared with negative NANOG expression (40 vs 120 months, respectively; P = 0.031).

CONCLUSIONS: Positive NANOG expression is associated with poor prognosis of ovarian serous carcinoma. NANOG has potential as a predictor of survival for patients with ovarian carcinomas and may be involved in the mechanism of chemoresistance.
Full Text
http://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&AN=00009577-201211000-00008&LSLINK=80&D=ovft
DOI
23095773
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Obstetrics and Gynecology (산부인과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Sang Wun(김상운) ORCID logo https://orcid.org/0000-0002-8342-8701
Kim, Sung Hoon(김성훈) ORCID logo https://orcid.org/0000-0002-1645-7473
Kim, Young Tae(김영태) ORCID logo https://orcid.org/0000-0002-7347-1052
Kim, Jae Hoon(김재훈) ORCID logo https://orcid.org/0000-0001-6599-7065
Nam, Eun Ji(남은지) ORCID logo https://orcid.org/0000-0003-0189-3560
Lee, Maria(이마리아)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/90474
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