Abstract

BackgroundGenomic deletion at tumor suppressor loci is a common genetic aberration in human cancers. The study aimed to explore candidate tumor suppressor genes at chromosome 4q25-q28.2 and to delineate novel prognostic biomarkers associated with colorectal cancer (CRC).MethodsDeletion mapping of chromosome 4q25-q28.2 was conducted in 114 sporadic CRC by loss of heterozygosity study with 11 microsatellite markers. A novel candidate tumor suppressor gene, namely NDST4, was identified at 4q26. Gene expression of NDST4 was investigated in 52 pairs of primary CRC tissues by quantitative reverse transcription-polymerase chain reaction. Allelic loss of NDST4 gene was further determined in 174 colorectal carcinomas by loss of heterozygosity analysis, and then was assessed for clinical relevance.ResultsOne minimal deletion region was delineated between D4S2297 and D4S2303 loci at 4q26, where NDST4 was the only gene that had markedly been downregulated in CRC tumors. By laser capture microdissection, NDST4 RNA expression was demonstrated in colonic epithelial cells, but was undetectable in tumor cells. In total, 30 (57.7%) of 52 colorectal carcinomas showed a dramatic reduction in NDST4 gene expression compared with matched normal mucosae. The genetic loss of NDST4 was significantly associated with advanced pathological stage (P = 0.039) and poorer overall survival of patients (P = 0.036).Conclusions NDST4 gene is a novel candidate tumor suppressor gene in human cancer, and the loss of its function might be involved in CRC progression. In addition, the loss of heterozygosity assay, which was established to determine the allelic loss of NDST4 gene, could be a cost-effective tool for providing a useful biomarker of adverse prognosis in CRC.

Highlights

  • Colorectal cancer (CRC) is one of the most common causes of cancer deaths worldwide, and most tumors arise sporadically by a combination of discrete mutations and chromosomal alterations [1,2,3]

  • Substantial studies have revealed that allelic losses on multiple regions of chromosome 4 are associated with stage progression, tumor metastasis, and shorter survival in many human cancers, indicating the presence of one or more tumor suppressor gene (TSG) loci [10,11,12,13,14,15]

  • One minimal deletion region with a genetic length of 1.4 Mb was delineated between D4S2297 and D4S2303, which was involved in 80.0% (40/50) of the tumors with loss of heterozygosity (LOH)

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Summary

Introduction

Colorectal cancer (CRC) is one of the most common causes of cancer deaths worldwide, and most tumors arise sporadically by a combination of discrete mutations and chromosomal alterations [1,2,3]. Despite aggressive operations supplemented with various adjuvant therapies and an increased understanding of the genetic mechanisms underlying this disorder, there has been little improvement in the survival of patients with invasive CRC [4,5]. Substantial studies have revealed that allelic losses on multiple regions of chromosome 4 are associated with stage progression, tumor metastasis, and shorter survival in many human cancers, indicating the presence of one or more tumor suppressor gene (TSG) loci [10,11,12,13,14,15]. Genomic deletion at tumor suppressor loci is a common genetic aberration in human cancers. The study aimed to explore candidate tumor suppressor genes at chromosome 4q25-q28.2 and to delineate novel prognostic biomarkers associated with colorectal cancer (CRC)

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