Title:
P53 gene: Mutation and immunohistochemical analysis in patients with invasive ductal carcinoma of breast

dc.contributor.authorShinjini Singh
dc.contributor.authorSandeep Kumar Rajput
dc.contributor.authorMritunjai Singh
dc.contributor.authorPravas Kumar Misra
dc.contributor.authorGyanendra Mohan
dc.contributor.authorMohan Kumar
dc.contributor.authorRakesh Kumar Singh
dc.contributor.authorIndrajeet Singh Gambhir
dc.date.accessioned2026-02-07T05:40:04Z
dc.date.issued2013
dc.description.abstractThe p53 tumor suppressor gene is the most commonly mutated gene in cancer. In breast cancer, the presence of p53 gene alterations has been associated with worse prognosis. This study was attempted to associate p53 gene mutations with its protein expression in North Eastern Indian population. We used single-stranded conformation polymorphism to screen samples for mutations in five conserved regions, exons 4, 5, 6, 7 and 8, of the p53 gene. Mutations were confirmed by direct DNA sequencing. Samples were also analyzed for expression of p53 immunohistochemically. We found two critical mutations in the exon 4. A well known missense mutation at codon 72 (pro to arg) with a frequency of 47% was found which was significantly correlated with the immunohistochemical analysis of p53 protein in such patients. A novel nonsense mutation at codon 107 which leads to stop codon was also found. Although the occurrence of this mutation was very less, we did not find expression of p53 protein immunohistochemicaly. We support that mutation in p53 gene can be exploited as a prognostic marker for the early diagnosis of breast cancer, although more clinical and epidemiological data is required to establish this claim. © 2013 Science Publication.
dc.identifier.doi10.3844/ajbbsp.2013.395.403
dc.identifier.issn15533468
dc.identifier.urihttps://doi.org/10.3844/ajbbsp.2013.395.403
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/24732
dc.subjectBreast cancer
dc.subjectER
dc.subjectHER2
dc.subjectp53
dc.subjectPR
dc.titleP53 gene: Mutation and immunohistochemical analysis in patients with invasive ductal carcinoma of breast
dc.typePublication
dspace.entity.typeArticle

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