Literature DB >> 17117392

OCT4: biological functions and clinical applications as a marker of germ cell neoplasia.

L Cheng1, M-T Sung, P Cossu-Rocca, T D Jones, G T MacLennan, J De Jong, A Lopez-Beltran, R Montironi, L H J Looijenga.   

Abstract

Germ cell tumours (GCTs) are a heterogeneous group of neoplasms, which develop in the gonads as well as in extragonadal sites, that share morphological patterns and an overall good prognosis, owing to their responsiveness to current surgical, chemotherapeutic, and radiotherapeutic measures. GCTs demonstrate extremely interesting biological features because of their close relationships with normal embryonal development as demonstrated by the pluripotentiality of some undifferentiated GCT variants. The similarities between GCTs and normal germ cell development have made it possible to identify possible pathogenetic pathways in neoplastic transformation and progression of GCTs. Genotypic and immunophenotypic profiles of these tumours are also useful in establishing and narrowing the differential diagnosis in cases of suspected GCTs. Recently, OCT4 (also known as OCT3 or POU5F1), a transcription factor that has been recognized as fundamental in the maintenance of pluripotency in embryonic stem cells and primordial germ cells, has been proposed as a useful marker for GCTs that exhibit features of pluripotentiality, specifically seminoma/dysgerminoma/germinoma and embryonal carcinoma. The development of commercially available OCT4-specific antibodies suitable for immunohistochemistry on paraffin-embedded specimens has generated increasing numbers of reports of OCT4 expression in a wide variety of gonadal and extragonadal GCTs. OCT4 immunostaining has been shown to be a sensitive and specific marker for seminomatous/(dys)germinomatous tumours and in embryonal carcinoma variants of non-seminomatous GCTs, whether in primary gonadal or extragonadal sites or in metastatic lesions. Therefore, OCT4 immunohistochemistry is an additional helpful marker both in the differential diagnosis of specific histological subtypes of GCTs and in establishing a germ cell origin for some metastatic tumours of uncertain primary. OCT4 expression has also been reported in pre-invasive conditions such as intratubular germ cell neoplasia, unclassified (IGCNU) and the germ cell component of gonadoblastoma. Additionally, OCT4 immunostaining shows promise as a useful tool in managing patients known to be at high risk for the development of invasive GCTs. Copyright (c) 2006 Pathological Society of Great Britain and Ireland.

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Year:  2007        PMID: 17117392     DOI: 10.1002/path.2105

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  72 in total

1.  Histological evidence for the existence of germ cell tumor cells showing embryonal carcinoma morphology but lacking OCT4 expression and cisplatin sensitivity.

Authors:  Thomas Mueller; Lutz Peter Mueller; Hans-Juergen Holzhausen; Ralf Witthuhn; Peter Albers; Hans-Joachim Schmoll
Journal:  Histochem Cell Biol       Date:  2010-06-08       Impact factor: 4.304

Review 2.  Advances in reprogramming somatic cells to induced pluripotent stem cells.

Authors:  Minal Patel; Shuying Yang
Journal:  Stem Cell Rev Rep       Date:  2010-09       Impact factor: 5.739

3.  Pure cartilaginous teratoma of the testis: an immunohistochemistry and fluorescence in situ hybridisation study.

Authors:  Ryan Des Jean; John N Eble; Shaobo Zhang; Liang Cheng
Journal:  J Clin Pathol       Date:  2007-06-29       Impact factor: 3.411

4.  A role for the Werner syndrome protein in epigenetic inactivation of the pluripotency factor Oct4.

Authors:  Johanna A Smith; Abibatou M N Ndoye; Kyla Geary; Michael P Lisanti; Olga Igoucheva; René Daniel
Journal:  Aging Cell       Date:  2010-05-10       Impact factor: 9.304

5.  Spontaneous metastasis in mouse models of testicular germ-cell tumours.

Authors:  J L Zechel; G T MacLennan; J D Heaney; J H Nadeau
Journal:  Int J Androl       Date:  2011-06-09

6.  Temporal analysis of neural differentiation using quantitative proteomics.

Authors:  Raghothama Chaerkady; Candace L Kerr; Arivusudar Marimuthu; Dhanashree S Kelkar; Manoj Kumar Kashyap; Marjan Gucek; John D Gearhart; Akhilesh Pandey
Journal:  J Proteome Res       Date:  2009-03       Impact factor: 4.466

7.  SALL4 is a useful marker in the diagnostic work-up of germ cell tumors in extra-testicular locations.

Authors:  Philippe Camparo; Eva Maria Comperat
Journal:  Virchows Arch       Date:  2012-12-09       Impact factor: 4.064

8.  High-level expression of stem cell marker CD133 in clear cell renal cell carcinoma with favorable prognosis.

Authors:  Kyungeun Kim; Hyojin Ihm; Jae Y Ro; Yong Mee Cho
Journal:  Oncol Lett       Date:  2011-08-02       Impact factor: 2.967

9.  A novel SRY missense mutation affecting nuclear import in a 46,XY female patient with bilateral gonadoblastoma.

Authors:  Remko Hersmus; Bertie H C G M de Leeuw; Hans Stoop; Pascal Bernard; Helena C van Doorn; Hennie T Brüggenwirth; Stenvert L S Drop; J Wolter Oosterhuis; Vincent R Harley; Leendert H J Looijenga
Journal:  Eur J Hum Genet       Date:  2009-06-10       Impact factor: 4.246

Review 10.  Concise review: isoforms of OCT4 contribute to the confusing diversity in stem cell biology.

Authors:  Xia Wang; Jianwu Dai
Journal:  Stem Cells       Date:  2010-05       Impact factor: 6.277

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