Evidence map›Paper›PMID 22116280›Full record

ArticleJournal of biosciences2011

TP53 gene polymorphism: importance to cancer, ethnicity and birth weight in a Brazilian cohort.

Helena S Thurow, Ricardo Haack, Fernando P Hartwig, Isabel O De Oliveira, Odir A Dellagostin, Denise P Gigante, Bernardo L Horta, Tiago Collares, Fabiana K Seixas

Abstract read
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In one paragraph

Article in Journal of biosciences, 2011. 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
1.0field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. The role of p53 in developmental syndromes.Journal of molecular cell biology · 2019
    Review
  3. Article
  4. High incidence of oncogenic HPV genotypes found in women from Southern Brazil.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2014
    Article
  5. Article
  6. Article
  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

9 authors at 2 institutions in 1 country.

Helena S ThurowFunctional Genomics Laboratory, Technology Development Centre (CDTec), Federal University of Pelotas (UFPel), Pelotas, RS, 96010-900, Brazil.
Ricardo Haack
Fernando P Hartwig
Isabel O De Oliveira
Odir A Dellagostin
Denise P Gigante
Bernardo L Horta
Tiago Collares
Fabiana K Seixas
Universidade Federal de Pelotas · BRFederal Center for Technological Education Celso Suckow da Fonseca · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Arg72Pro SNP of p53 has been associated with many types of cancer as well as with survival and longevity. We evaluated the Arg72Pro SNP frequencies of a Brazilian birth cohort and their association with current, demographic and birth epidemiological parameters available. In 1982, all hospital births of Pelotas, southern Brazil, were identified and studied prospectively. In 2004-5, blood samples were collected and DNA extracted. PCR-RFLP was used to genotype the Arg72Pro SNP in 3794 individual samples of the Brazil birth cohort and DNA sequencing was performed to confirm the genotypes. The genotype distribution, which was in Hardy-Weinberg equilibrium, showed a predominance of the arginine amino acid with a frequency of 46.9% Arg/Arg, 42.2% Arg/Pro and 10.9% Pro/Pro. The allele frequency was 0.68 of Arginine and 0.32 of Proline. The Arg72Pro SNP genotype and allelic frequency were related to skin colour where proline amino acid was observed more among black subjects, while arginine amino acid was observed more among white subjects. The individuals without family history of cancer and those with low birth weight were associated with arginine amino acid. The Arg72Pro SNP was strongly associated with important epidemiological variables confirming that genetic profiles on cohort studies can improve our understanding of the susceptibility of diseases and its risk factors.

Indexed as

Polymorphism, Single NucleotideAmino Acid SubstitutionBirth WeightBlack PeopleBrazilCohort StudiesFemaleGene FrequencyGenetic Association StudiesGenotypeHumansMaleNeoplasmsSequence Analysis, DNATumor Suppressor Protein p53White PeopleTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID22116280
OpenAlexW1964784370

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.