Prognostic significance of microsatellite alterations at 1p36 in cholangiocarcinoma.

World J Gastroenterol

Department of Clinical Chemistry, Center for Research and Development of Medical Diagnostic Laboratories, Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen 40002, Thailand.

Published: July 2006

AI Article Synopsis

  • The study investigates loss of heterozygosity (LOH) and microsatellite instability (MSI) on chromosome 1p36 in cholangiocarcinoma (CCA) patients, linking these genetic alterations to clinical outcomes.
  • Out of 90 patients, 75.6% exhibited LOH at various loci, with specific markers like D1S199 and D1S507 showing the highest frequencies, while 37.8% showed MSI, indicating potential tumor suppressor genes in the region.
  • The research suggests that certain LOH and MSI patterns are associated with clinical features like lymphatic and nerve invasion, and that these genetic changes may serve as useful prognostic indicators for CCA patients.

Article Abstract

Aim: To investigate loss of heterozygosity (LOH) and microsatellite instability (MSI) on the chromosomal region 1p36-pter in cholangiocarcinoma (CCA) patients and determine the association between microsatellite alterations and clinicopathological parameters.

Methods: Ten polymorphic microsatellite markers were determined for LOH and MSI using GS-3000 gel scan fragment autoanalyzer.

Results: Sixty-eight out of 90 cases (75.6%) showed LOH in one or more loci. LOH was found most frequently at D1S199 (40.0%), D1S507 (34.6%), D1S2845 (30.5%), and D1S2734 (30.1%). MSI was found in 34 of 90 cases (37.8%) at one or more loci. Fine mapping at 1p36 showed two distinctive regions of common loss, which were D1S2845 and the 25.5-cM region between D1S507 and D1S2734, indicating the existence of putative tumor suppressor genes that is likely to play important roles in the development of CCA. Patients with LOH at D1S234 showed less lymphatic invasion (P = 0.017), whereas patients with LOH at D1S2676 exhibited more lymphatic invasion than those without (P = 0.031). LOH at D1S2845 showed a significant correlation with nerve invasion (P = 0.029). Moreover, patients who demonstrated MSI at D1S228 showed a poor prognosis (P = 0.0026).

Conclusion: Allelic loss plays a major role in microsatellite alterations at chromosome 1p36, which may contribute to carcinogenesis and pathogenesis of liver fluke related CCA and these alterations can be used as molecular prognostic indicators for CCA patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4087750PMC
http://dx.doi.org/10.3748/wjg.v12.i27.4377DOI Listing

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