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PMID: 15330191 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The expression and prognostic value of alpha-, beta- and gamma-catenins in renal cell carcinoma.

Anticancer research ·Vol. 24 ·No. 4 ·2004-00-00 ·Pages 2407-13

Aaltomaa S, Lipponen P, Kärjä V, Lundstedt S, Lappi J, Kosma VM

Abstract

Catenins have prognostic value in several human tumours. The aim of the study was to analyse the prognostic value of catenin expression in a prospectively followed series of renal cell carcinoma. One hundred and twenty-four renal cell carcinomas were prospectively followed-up for a mean of 3.5 years and the survival data of patients were related to standard prognostic factors and to the results of alpha-, beta- and gamma-catenin immunohistochemistry. The data of catenin immunohistochemistry were also related to the clinical and histopathological characteristics of the tumours. Low cytoplasmic alpha-catenin expression was related to lymphatic tumour growth (p=0.02) and to tumour necrosis (p=0.02). The weak expression intensity of beta-catenin on cell membranes was related to venous growth inside the tumour (p=0.02), extratumoural venous growth (p=0.03) and to perineural growth (p<0.001). Nuclear gamma-catenin expression was strongly associated with clear cell type (p=0.0001) and high WHO grade (p=0.038). Short recurrence-free survival was predicted by weak membranous alpha-catenin (p=0.015) and beta-catenin (p=0.006) expression intensity, while their cytoplasmic expression was of lower significance (p=0.07 and 0.045, respectively). All the conventional prognostic factors predicted short recurrence-free survival: Fuhrman classification (p=0.02), WHO grade (p=0.026), perineural growth (p=0.013), venous invasion (p=0.0024), tumour size (p=0.004) and T-category (p=0.0001). Independent predictors of short recurrence-free survival were weak membranous expression intensity of beta-catenin (RR=0.15, p=0.004), high T-category (RR=2.70, p=0.0001) and high WHO grade (RR=2.24, p=0.025). The results show that immunohistochemical analysis of beta-catenin expression may be used as an indicator of aggressiveness in renal cell carcinoma.

MeSH Terms
Adult Aged Aged, 80 and over Carcinoma, Renal Cell/blood supply,metabolism,pathology Cytoskeletal Proteins/biosynthesis Desmoplakins Female Follow-Up Studies Humans Kidney Neoplasms/blood supply,metabolism,pathology Male Middle Aged Prognosis Prospective Studies Trans-Activators/biosynthesis alpha Catenin beta Catenin gamma Catenin
Chemicals
CTNNA1 protein, human CTNNB1 protein, human Cytoskeletal Proteins Desmoplakins JUP protein, human Trans-Activators alpha Catenin beta Catenin gamma Catenin
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Aaltomaa Sirpa
Department of Surgery and Urology, Kuopio University Hospital, Kuopio, Finland. sirpa.aaltomaa@kuh.fi
Lipponen Pertti
Kärjä Vesa
Lundstedt Seppo
Lappi Jani
Kosma Veli-Matti
Article Info
Journal
Anticancer research
Abbr.
Anticancer Res
ISSN
0250-7005
Published
2004-00-00
Pages
2407-13
Language
English
Region
Greece
NLM ID
8102988
Subset
IM
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