Expression of MRP14 gene is frequently down-regulated in Chinese human esophageal cancer

Jie Wang1, Yan Cai, Hao Xu

  • 1National Laboratory of Molecular Oncology, Cancer Institute (Hospital), Chinese Academy of Medical Sciences, Peking University of Medical School, Beijing 100021, China.

Cell Research
|March 26, 2004
PubMed

Insights

Migration inhibitory factor-related protein 14 (MRP14) expression is significantly reduced in human esophageal cancer. This down-regulation of MRP14 suggests its potential role as a biomarker in esophageal cancer development.

Area of Science:

  • Oncology
  • Molecular Biology
  • Biochemistry

Background:

  • Migration inhibitory factor-related protein 14 (MRP14), also known as S100A9, is a calcium-binding protein.
  • The MRP8/14 complex functions as a major fatty acid carrier in neutrophils and is involved in arachidonic acid transport in keratinocytes.

Purpose of the Study:

  • To investigate the involvement of MRP14 in human esophageal cancer.
  • To determine the expression levels of MRP14 in esophageal tumors compared to normal tissues.

Main Methods:

  • Differential display-reverse transcription polymerase chain reaction (DD-PCR) for initial screening.
  • Northern blotting, RT-PCR, and Western blotting to corroborate MRP14 down-regulation.
  • Immunohistochemistry and DNA sequencing to assess protein localization and gene mutations.

Main Results:

  • MRP14 expression was significantly decreased or undetectable in 58/64 squamous cell carcinomas and 2/2 adenocarcinomas.
  • MRP14 was absent in all tested esophageal carcinoma cell lines.
  • Immunohistochemistry confirmed MRP14 expression restricted to normal esophageal epithelia, with no mutations found in the MRP14 gene.

Conclusions:

  • Reduced expression of MRP14 is a frequent event in Chinese human esophageal cancer.
  • The down-regulation of MRP14 suggests its potential role in esophageal tumorigenesis.
  • MRP14 may serve as a potential diagnostic or prognostic biomarker for esophageal cancer.

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