Splice Site and Germline Variations of the MGMT Gene in Esophageal Cancer from Kashmir Valley : India
Author(s) -
Mohd Amin Shah,
Sheikh Shaffi,
Ghulam Nabi Lone
Publication year - 2013
Publication title -
international journal of health sciences
Language(s) - English
Resource type - Journals
eISSN - 1658-7774
pISSN - 1658-3639
DOI - 10.12816/0006055
Subject(s) - esophageal cancer , genotyping , exon , germline mutation , germline , genetics , gene , biology , genotype , coding region , genetic variation , cancer , intron , medicine , cancer research , mutation
OBJECTIVESThe aim of our investigation was to detect mutation or genetic polymorphisms in MGMT gene of esophageal cancer patients from Kashmir Valley (India).METHODOLOGYThe genetic polymorphisms or mutations in the coding exons 2, 3, 4 and 5 of MGMT gene were searched for in DNA samples from the frozen tumor tissues of 30 esophageal cancer patients from Kashmir. The PCR products were sequenced with fluorescently labelled terminators and separated on automatic sequencer. We developed a new PCR based RFLP approach for genotyping c.459A>G (p.Gly153Gly) variation in 71 esophageal cancer patients and 60 healthy controls.RESULTSTwo somatic variations c.274 +4G>A and c.274 + 22G>A were identified in Exon3-intron 4 boundary. A novel germline variation c.459A>G (p.Gly153Gly) was found in the exon 5 of an esophageal cancer patient. This germline variation was not found in any of the studied esophageal cancer patients and healthy controls except the patient where it has been found by direct sequencing.CONCLUSIONWe identified novel sequence variants of the MGMT gene in esophageal cancer patients from Kashmir valley-India.
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