The pluripotency homeobox gene NANOG is expressed in human germ cell tumors

被引:221
作者
Hart, AH
Hartley, L
Parker, K
Ibrahim, M
Looijenga, LHJ
Pauchnik, M
Chow, CW
Robb, L
机构
[1] Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
[2] Univ Rotterdam, Dept Pathol, Erasmus MC,Daniel Hoed Canc Ctr, Med Ctr,Josephine Nefkens Inst, Rotterdam, Netherlands
[3] Royal Childrens Hosp, Dept Anat Pathol, Melbourne, Vic, Australia
关键词
germ cells; NANOG protein; pou5f1 transcription factor; neoplasms; germ cell; embryonal;
D O I
10.1002/cncr.21435
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. The NANOG gene, a member of the homenbox family of DNA binding transcription factors, was recently identified in a screen for pluripotency-promoting genes. NANOG overexpression in routine embryonic stem cells is sufficient to maintain self-renewal and to block differentiation. The NANOG gene is located on human chromosome 12p13, a region frequently duplicated in human tumors of germ cell origin and in cultured human embryonic stem cells. Here we investigate the expression and gene copy number of NANOG in human germ cells and tumors of germ cell origin. METHODS. Immunohistochemistry and quantitative polymerase chain reaction (QPCR) were used to examine the expression and gene copy number of the human NANOG gene in germ cell tumors. RESULTS. NANOG protein was detected in germline stem cells (gonocytes) within the developing testis. Immunohistochemistry and quantitative real-time PCR analysis were used to demonstrate that NANOG is highly and specifically expressed in carcinoma in situ (CIS), embryonal carcinomas, and seminomas, but not in teratomas and yolk sac tumors. CONCLUSIONS. NANOG expression in germline stem cells (gonocytes), CIS, embryonal carcinoma, and seminoma reveals a molecular and developmental link between germ cell tumors and the embryonic cells from which they arise. Identification of NANOG as a molecular marker of undifferentiated germ cell tumors provides a novel tool for identifying and classifying tumors of germ cell origin. (c) 2005 American Cancer Society.
引用
收藏
页码:2092 / 2098
页数:7
相关论文
共 37 条
[1]   Embryonic stem cell-like features of testicular carcinoma in situ revealed by genome-wide gene expression profiling [J].
Almstrup, K ;
Hoei-Hansen, CE ;
Wirkner, U ;
Blake, J ;
Schwager, C ;
Ansorge, W ;
Nielsen, JE ;
Skakkebæk, NE ;
Meyts, ERD ;
Leffers, H .
CANCER RESEARCH, 2004, 64 (14) :4736-4743
[2]   Genome-wide gene expression profiling of testicular carcinoma in situ progression into overt tumours [J].
Almstrup, K ;
Hoei-Hansen, CE ;
Nielsen, JE ;
Wirkner, U ;
Ansorge, W ;
Skakkebæk, NE ;
Rajpert-De Meyts, E ;
Leffers, H .
BRITISH JOURNAL OF CANCER, 2005, 92 (10) :1934-1941
[3]   CHROMOSOME 12-CONTAINING MARKERS, INCLUDING 2 DICENTRICS, IN 3 I(12P)-NEGATIVE TESTICULAR GERM-CELL TUMORS [J].
ATKIN, NB ;
FOX, MF ;
BAKER, MC ;
JACKSON, Z .
GENES CHROMOSOMES & CANCER, 1993, 6 (04) :218-221
[4]   Self-renewal of teratocarcinoma and embryonic stem cells [J].
Chambers, I ;
Smith, A .
ONCOGENE, 2004, 23 (43) :7150-7160
[5]   Functional expression cloning of Nanog, a pluripotency sustaining factor in embryonic stem cells [J].
Chambers, I ;
Colby, D ;
Robertson, M ;
Nichols, J ;
Lee, S ;
Tweedie, S ;
Smith, A .
CELL, 2003, 113 (05) :643-655
[6]   Establishing a germ cell origin for metastatic tumors using OCT4 immunohistochemistry [J].
Cheng, L .
CANCER, 2004, 101 (09) :2006-2010
[7]   Expression of interleukin-11 during the human menstrual cycle: coincidence with stromal cell decidualization and relationship to leukaemia inhibitory factor and prolactin [J].
Dimitriadis, E ;
Salamonsen, LA ;
Robb, L .
MOLECULAR HUMAN REPRODUCTION, 2000, 6 (10) :907-914
[8]   Pluripotential stem cells derived from migrating primordial germ cells [J].
Durcova-Hills, G ;
Ainscough, JFX ;
McLaren, A .
DIFFERENTIATION, 2001, 68 (4-5) :220-226
[9]   Immunohistochemical profiling of germ cells within the human fetal testis: Identification of three subpopulations [J].
Gaskell, TL ;
Esnal, A ;
Robinson, LLL ;
Anderson, RA ;
Saunders, PTK .
BIOLOGY OF REPRODUCTION, 2004, 71 (06) :2012-2021
[10]   Identification, cloning and expression analysis of the pluripotency promoting Nanog genes in mouse and human [J].
Hart, AH ;
Hartley, L ;
Ibrahim, M ;
Robb, L .
DEVELOPMENTAL DYNAMICS, 2004, 230 (01) :187-198