Evidence map›Paper›PMID 28208862›Full record

ArticleJournal of clinical and diagnostic research : JCDR2016

Correlation of p53 Overexpression with the Clinicopathological Prognostic Factors in Colorectal Adenocarcinoma.

Akshatha C, Vijaya Mysorekar, Arundhathi S, Arul P, Adithi Raj, Smitha Shetty

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical and diagnostic research : JCDR, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 8 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Akshatha CAssistant Professor, Department of Pathology, Dhanalakshmi Srinivasan Medical College and Hospital , Perambalur, Tamilnadu, India .
Vijaya MysorekarProfessor and HOD, Department of Pathology, MS Ramaiah Medical College and Hospital , Bengaluru, Karnataka, India .
Arundhathi SLecturer, Department of Pathology, Sanjay Gandhi Institute of Trauma and Orthopedics , Bengaluru, Karnataka, India .
Arul PAssistant Professor, Department of Pathology, Dhanalakshmi Srinivasan Medical College and Hospital , Perambalur, Tamilnadu, India .
Adithi RajSenior resident, Department of Pathology, Indira Gandhi Institute of Child Health , Banglore, Bengaluru, Karnataka, India .
Smitha ShettyAssistant Professor, Department of Pathology, Dhanalakshmi Srinivasan Medical College and Hospital , Perambalur, Tamilnadu, India .
Dhanalakshmi Srinivasan Group of Institutions · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMutation in p53 gene and accumulation of p53 protein is a common genetic event in colorectal carcinomas. p53 mutation can be detected by various techniques such as DNA sequencing, polymerase chain reaction and immunohistochemistry (IHC). However, IHC is simple and is consistent with other techniques.

aimTo establish a correlation between overexpression of p53 with the clinical features, tumour histopathology and stage of Colorectal Carcinoma (CRC). MATERIALS AND

methodsThis prospective and retrospective study of clinical, histopathological and IHC features of CRC was conducted on colectomy and abdomino-perineal resection specimens received from January 2008 to June 2013. For each case, the clinical features, tumour morphology and p53 status (by IHC) were evaluated.

resultsThe most common histologic type of CRC was Non-Specific Type (NST) and grade II tumours were seen predominantly (60%). Overall, 67.5% of CRCs showed p53 positivity on IHC. Intense p53 positivity was observed in 37.5% of CRCs of NST type and 33.3% of mucinous adenocarcinomas showed moderate positivity. Grade III tumours showed variable p53 positivity and those with lymph node metastasis showed moderate (55.6%) or intense positivity (53.8%). But there was no statistically significant correlation of p53 status and various clinicopathological prognostic factors.

conclusionAs p53 protein overexpression is seen in a relatively high percentage of CRCs, it seems that p53 mutation plays an important role in development of CRC. However, no direct correlation could be established between p53 results and the patients' age, sex, tumour site, size, histological type, grade, lymph node status, or TNM stage. A prolonged follow up is necessary to conclude whether p53 status has any influence on the long, term prognosis and patient survival.

Indexed as

Genetic AlterationsGradeImmunohistochemistryp53TNM stage

Identifiers

PMID28208862
PMCPMC5296435
OpenAlexW2565551442

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Registered trials

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