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Updated: Aug 25, 2026

Development of Compendium for Esophageal Squamous Cell Carcinoma
Published on: April 12, 2024
Expression of MRP14 gene is frequently down-regulated in Chinese human esophageal cancer
1National Laboratory of Molecular Oncology, Cancer Institute (Hospital), Chinese Academy of Medical Sciences, Peking University of Medical School, Beijing 100021, China.
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.
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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