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

Jie Wang, Yan Cai, Hao Xu, Jun Zhao, Xin Xu, Ya Ling Han, Zhi Xiong Xu, Bao Sheng Chen, Hai Hu, Min Wu, Ming Rong Wang

Research output: Contribution to journalArticlepeer-review

30 Scopus citations

Abstract

Migration inhibitory factor-related protein 14 (MRP14) is one of calcium-binding proteins, referred as S100A9. The heterodimeric molecule formed by MRP14 with its partner MRP8 (S100A8) is the major fatty acid carrier in neutrophils. The MRP8/14 complex has been also implicated in the intracellular transport of arachidonic acid and its precursors in keratinocytes. We show here the involvement of MRP14 in human esophageal cancer. In an initial study, mRNA differential display - reverse transcription polymerase chain reaction (DD-PCR) was performed with two esophageal carcinomas, one esophageal adenocarcinoma and matched normal adjacent mucosa. DD-PCR with the arbitrary primer OPA3 showed that one cDNA band was highly expressed in normal tissues, but disappeared or substantially decreased in tumor counterparts. It was later identified to be the 3'-end of migration inhibitory factor-related protein 14 (MRP14). Northern blotting, RT-PCR and Western blotting corroborated the down-regulation of MRP14 in 58/64 squamous cell carcinomas and 2/2 adenocarcinomas as compared with adjacent normal epithelia of the esophagus. MRP14 was undetectable in 3/3 esophageal-carcinoma cell lines. Immunochemistry demonstrated that expression of MRP14 was restricted to normal esophageal epithelia. No mutation was found in the genomic DNA of the MRP14 gene by PCR and directed DNA sequencing. Our finding suggested that the reduction of MRP14 expression is a frequent event in Chinese human esophageal cancer.

Original languageEnglish
Pages (from-to)46-53
Number of pages8
JournalCell Research
Volume14
Issue number1
DOIs
StatePublished - Feb 2004

Keywords

  • Carcinoma
  • Esophagus
  • MRP14
  • S100A9

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