Evidence map›Paper›PMID 26005655›Full record

ArticleIranian journal of public health2014

The TP53 Codon 72 Polymorphism and Risk of Sporadic Prostate Cancer among Iranian Patients.

Farhad Babaei, Seyed Ali Ahmadi, Ramin Abiri, Farhad Rezaei, Maryam Naseri, Mahmoud Mahmoudi, Rakhshande Nategh, Talat Mokhtari Azad

Abstract read
In one paragraph

Article in Iranian journal of public health, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Association ofBioMed research international · 2022
    Article
  5. Article
  6. Review
  7. Article
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

8 authors.

Farhad Babaei1. Dept. of Virology, School of Public Health, Tehran University of Medical Sciences , Tehran, Iran.
Seyed Ali Ahmadi2. School of Medicine, Tehran University of Medical Sciences , Tehran, Iran.
Ramin Abiri3. Dept. of Microbiology, School of Medicine, Kermanshah University of Medical Sciences , Kermanshah, Iran.
Farhad Rezaei1. Dept. of Virology, School of Public Health, Tehran University of Medical Sciences , Tehran, Iran.
Maryam Naseri1. Dept. of Virology, School of Public Health, Tehran University of Medical Sciences , Tehran, Iran.
Mahmoud Mahmoudi4. Dept. of Epidemiology and Biostatistics, School of Public Health, Tehran University of Medical Sciences , Tehran, Iran.
Rakhshande Nategh1. Dept. of Virology, School of Public Health, Tehran University of Medical Sciences , Tehran, Iran.
Talat Mokhtari Azad1. Dept. of Virology, School of Public Health, Tehran University of Medical Sciences , Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe TP53 gene is one of the most frequently mutated genes amongst human malignancies, particularly TP53 codon 72 polymorphism. Furthermore, an association between the TP53 codon 72 variants and prostate cancer has been reported in several studies. Although some studies have indicated an association between the TP53 Arg/Arg variant and an increased risk for prostate cancer, other studies have shown a positive correlation between the TP53 Pro/Pro genotype instead. Therefore, to clarify if this polymorphism is associated with an increased risk of prostate cancer in Iranian men, we conducted a case-control study of 40 sporadic prostate cancer patients and 80 benign prostate hyperplasia cases.

methodsThe TP53 codon 72 was genotyped using an allele specific PCR.

resultsA significant association between the TP53 codon 72 genotype and prostate cancer risk was found (OR = 6.8, 95% CI = [1.8-25.1], P = 0.005). However, the results of this study did not support an association between age, the Gleason score nor TP53 genotype at codon 72 in prostate cancer patients.

conclusionsTP53 codon 72 polymorphism may have a great impact in the development of prostate cancer.

Indexed as

Benign prostate hyperplasiaSporadic prostate cancerTP53 codon 72 polymorphism

Identifiers

PMID26005655
PMCPMC4433726

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.