Evidence map›Paper›PMID 24464128›Full record

ArticleMolecular biology reports2014

Association of mutation and hypermethylation of p21 gene with susceptibility to breast cancer: a study from north India.

Naseem Akhter, Md Salman Akhtar, Md Margoob Ahmad, Shafiul Haque, Sarah Siddiqui, Syed Ikramul Hasan, Nootan K Shukla, Syed Akhtar Husain

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Article in Molecular biology reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 42% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors at 4 institutions in 3 countries.

Naseem AkhterDepartment of Biotechnology, Jamia Millia Islamia, New Delhi, India.
Md Salman Akhtar
Md Margoob Ahmad
Shafiul Haque
Sarah Siddiqui
Syed Ikramul Hasan
Nootan K Shukla
Syed Akhtar Husain
Department of Biotechnology · INJamia Millia Islamia · INAll India Institute of Medical Sciences · INUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

p21 gene located at chromosome 6p21.2 is a possible tumour suppressor gene involved in the pathogenesis of breast cancer. Both genetic and epigenetic alterations in p21 have been implicated in breast carcinoma. In the present study, our main aim was to study the impact of these two kinds of alterations of p21 gene in Indian female breast cancer patients. A total of 150 female breast cancer patients of north India were screened by PCR-SSCP followed by direct sequencing and methylation specific PCR. Mutational screening of p21 gene revealed significant amount of mutations [32.66% (49/150)] in exon 2, whereas p21 promoter was found hypermethylated in 42 of 150 (28%) breast cancer patients in our population. The intriguing feature of the study was the G>T transition (GAG>TAG) at codon 107 and the A>C transition (AGC>CGC) at codon 146 possibly rendering p21 completely ineffective in its anti- proliferative activity. Our results suggest a significant association between the mutational and hypermethylation profile of p21 gene. Therefore, we show for the first time that the significant association of p21 mutation and hypermethylation leads to the complete inactivation of p21 gene in Indian female breast cancer patients. Complete silencing of the p21 gene seems to be the result not only of genetic alterations but also of epigenetic modification.

Indexed as

DNA MethylationGenetic Predisposition to DiseaseMutationBreast NeoplasmsCyclin-Dependent Kinase Inhibitor p21DNA Mutational AnalysisExonsFemaleGene Expression ProfilingHumansIndiaPromoter Regions, GeneticCyclin-Dependent Kinase Inhibitor p21

Identifiers

PMID24464128
OpenAlexW1972368989

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.