ArticleSaudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association
Molecular gate keepers succumb to gene aberrations in colorectal cancer in Kashmiri population, revealing a high incidence area.
Article in Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
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14 citing papers in PubMed, 27 citations in OpenAlex.
- Squamous cell carcinoma of the sigmoid colon: a rare case report.Journal of surgical case reports · 2025Article
- Non-conventional mucosal lesions (serrated epithelial change, villous hypermucinous change) are frequent in patients with inflammatory bowel disease-results of molecular and immunohistochemical single institutional study.Virchows Archiv : an international journal of pathology · 2020Article
- Coexistence ofCell journal · 2017Article
- Role of genetic & environment risk factors in the aetiology of colorectal cancer in Malaysia.The Indian journal of medical research · 2014Article
- Genetic unraveling of colorectal cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014Review
- Colorectal cancer: a researcher's perspective of the molecular angel's gone eccentric in the Vale of Kashmir.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2013Review
- Coexistence of two different mutations in codon 12 of the Kras gene in colorectal cancer: Report of a case supporting the concept of tumoral heterogeneity.Oncology letters · 2013Article
- KRAS gene mutations in correlation with clinicopathological features of colorectal carcinomas in Indian patient cohort.Medical oncology (Northwood, London, England) · 2013Article
- Role of CYP2E1 genotypes in susceptibility to colorectal cancer in the Kashmiri population.Human genomics · 2011Article
- Multiple mutations in the Kras gene in colorectal cancer: review of the literature with two case reports.International journal of colorectal disease · 2011Review
- Mutations of p53 and K-ras correlate TF expression in human colorectal carcinomas: TF downregulation as a marker of poor prognosis.International journal of colorectal disease · 2011Article
- Squamous cell carcinoma of rectum presenting in a man: a case report.Journal of medical case reports · 2010Article
- Article
- KRAS and TP53 mutations in colorectal carcinoma.Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology AssociationArticle
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8 authors at 1 institution in 1 country.
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Abstract
BACKGROUND/
aimColorectal cancer (CRC) is one of the leading malignancies worldwide and has been reported to show geographical variation in its incidence, even within areas of ethnic homogeneity. The aim of this study was to identify p53 and K-ras gene mutations in CRC patients in a Kashmiri population, and to assess whether these mutations are linked with clinicopathological parameters. MATERIALS AND
methodsPaired tumor and normal tissue samples from a consecutive series of 53 patients undergoing resective surgery for CRC were prospectively studied for p53 and K-ras gene mutations by PCR/single strand conformation polymorphism (SSCP).
resultsLess than half (45%, 19/42) of the patients presented mutations in the p53 gene. Twenty eight mutations were found in the p53 gene, which comprised of 23 substitutions (17 transitions + 6 transversions), and five insertions. The 23 substitutions constituted 18 missense mutations, two nonsense mutations, and three silent mutations. Of the 28 mutations (7.14%) observed in this study, 2 were not previously reported for CRC samples and were identified as novel p53 mutations. A few patients (22.64%, 12/53) presented with mutations in K-ras, constituting 13 missense mutations, out of which 11 were G-->A transitions, one was a G-->C transversion, and one a G-->T transversion. More than half (61.5%) of the mutations occurred in codon 12 whereas a few (38.5%) occurred in codon 13. One tumor contained missense mutations in both codons. Comparison of the mutation profiles of our patients with those of other ethnic populations and regions reflected both differences and similarities, indicating co-exposure to a unique set of risk factors.
conclusionMutations of the p53 and K-ras genes are some of the most common genetic changes in the development of human CRC. The high frequency of p53 gene mutations implicates p53 as a predominant factor for CRC in the high-risk ethnic Kashmiri population.
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