Literature DB >> 9792156

CD44v3 and v6 variant isoform expression correlates with poor prognosis in early-stage vulvar cancer.

C Tempfer1, G Sliutz, G Haeusler, P Speiser, A Reinthaller, G Breitenecker, N Vavra, C Kainz.   

Abstract

Expression of alternatively spliced CD44 isoforms has been reported to correlate with poor prognosis in human squamous cell cancers, i.e. squamous cell cancer of the lung and cervix. The aim of this study was to evaluate whether CD44 isoform expression is a prognostic factor in early-stage squamous cell cancer of the vulva. Seventy cases of squamous cell carcinoma of the vulva International Federation of Gynaecology and Obstetrics (FIGO) stage I were examined immunohistochemically for expression of CD44 isoforms. We used four different variant exon sequence-specific murine monoclonal antibodies to epitopes encoded by exons v3, v5, v6 and v7-8 of human variant CD44. The correlation of CD44 expression with histological grade and disease-free and overall survival was investigated. CD44 isoforms CD44v3, CD44v5, CD44v6 and CD44v7-8 were detected in 28% (20/70), 47% (33/70), 33% (23/70) and 17% (12/70) of the tumour samples respectively. Patients suffering from tumours expressing CD44v6 had a poorer relapse-free (log-rank test, P = 0.02) and overall survival (log-rank test, P = 0.03). Likewise, patients suffering from tumours expressing CD44v3 had a poorer relapse-free (log-rank test, P = 0.04) and overall survival (log-rank test, P = 0.01). Expression of CD44v5 and CD44v7-8 did not compromise the patients' outcome. Histological grade did not correlate with CD44 isoform expression. Immunohistochemically detected expression of CD44 isoforms containing variant exon v6 or v3 is correlated with a poor relapse-free and overall survival in FIGO stage I vulvar cancer patients.

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Year:  1998        PMID: 9792156      PMCID: PMC2063157          DOI: 10.1038/bjc.1998.633

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  17 in total

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Journal:  Lancet       Date:  1995-03-11       Impact factor: 79.321

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Journal:  Int J Cancer       Date:  1995-02-08       Impact factor: 7.396

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Journal:  Br J Cancer       Date:  1993-08       Impact factor: 7.640

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Journal:  J Cell Biol       Date:  1993-07       Impact factor: 10.539

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