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The immunohistochemical expression of STAT3, Bcl-xL, and MMP-2 proteins in colon adenoma and adenocarcinoma

  • Seung Woo Lee
  • , Young Yong Ahn
  • , Yon Soo Kim
  • , Sang Beum Kang
  • , Soon Woo Nam
  • , Dong Soo Lee
  • , Hyun Yong Jeong
  • , Jin Man Kim
  • The Catholic University of Korea, College of Medicine
  • Chungnam National University

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

Background/Aims: Signal transducers and activators of transcription (STATs) are a family of transcription factors that are activated in response to cytokines and growth factors. STAT3 activation has been implicated in modulating the activity of downstream mediators, such as Bcl-xL and matrix metalloproteinase-2 (MMP-2). The aim of this study was to investigate the immunohistochemical expression of STAT3, B-cell lymphoma-extra large (Bcl-xL), and MMP-2 proteins according to histopathological parameters in colon adenocarcinomas, including lymph node metastasis, tumor differentiation, the TNM stage and the tumor size. Methods: Immunohistochemical staining with monoclonal STAT3, Bcl-xL, and MMP-2 antibodies was performed on paraffin-embedded specimens from 20 colon adenomas and 39 adenocarcinomas. Results: The expression of STAT3, Bcl-xL, and MMP-2 was increased in the adenocarcinomas as compared with the adenomas (p>0.001). STAT3 expression was stronger in tumors with a distant metastasis than in tumors without a distant metastasis (p=0.012). A larger tumor size was related to an increase in STAT3 expression (p=0.035). Conclusions: STAT3, Bcl-xL, and MMP-2 may play important roles in the tumorigenesis of colorectal carcinoma. STAT3 may be indicative of a poor prognosis due to its correlation with distant metastases and a larger tumor size.

Original languageEnglish
Pages (from-to)45-51
Number of pages7
JournalGut and Liver
Volume6
Issue number1
DOIs
StatePublished - Jan 2012

Keywords

  • B-cell lymphoma-extra large
  • Colon
  • Matrix metalloproteinase-2
  • Signal transducers and activators of transcription 3

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