Evidence map›Paper›PMID 36083231›Full record

ArticleCancer science2022

p53 Arg72Pro polymorphism, adiposity status, and cancer risk: Two case-cohorts within a Japanese prospective study.

Shiori Nakano, Taiki Yamaji, Ryoko Katagiri, Norie Sawada, Manami Inoue, Shoichiro Tsugane, Motoki Iwasaki, Japan Public Health Center-based Prospective Study Group

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 53% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Review
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 at 1 institution in 1 country.

Shiori NakanoDivision of Epidemiology, National Cancer Center Institute for Cancer Control, Tokyo, Japan.ORCID https://orcid.org/0000-0001-5762-850X
Taiki YamajiDivision of Epidemiology, National Cancer Center Institute for Cancer Control, Tokyo, Japan.ORCID https://orcid.org/0000-0002-4799-8782
Ryoko KatagiriDivision of Epidemiology, National Cancer Center Institute for Cancer Control, Tokyo, Japan.
Norie SawadaDivision of Cohort Research, National Cancer Center Institute for Cancer Control, Tokyo, Japan.ORCID https://orcid.org/0000-0002-9936-1476
Manami InoueDivision of Prevention, National Cancer Center Institute for Cancer Control, Tokyo, Japan.ORCID https://orcid.org/0000-0003-1276-2398
Shoichiro TsuganeDivision of Cohort Research, National Cancer Center Institute for Cancer Control, Tokyo, Japan.
Motoki IwasakiDivision of Epidemiology, National Cancer Center Institute for Cancer Control, Tokyo, Japan.ORCID https://orcid.org/0000-0003-3319-4131
Japan Public Health Center-based Prospective Study Group
National Institute of Infectious Diseases · JP

Funding

Japan Agency for Medical Research and Development JP16ck0106095Japan Agency for Medical Research and Development JP19ck0106266Japan Agency for Medical Research and Development JP22ck0106551Ministry of Health, Labour, and Welfare of JapanNational Cancer Center Research and Development Fund 2020-J-4National Cancer Center Research and Development Fund 2022-A-20National Cancer Center Research and Development Fund 23-A-31National Cancer Center Research and Development Fund 26-A-2National Cancer Center Research and Development Fund 28-A-19National Cancer Center Research and Development Fund 29-A-4National Cancer Center Research and Development Fund 31-A-18
6 · The paper itself

Abstract

The tumor suppressor protein, p53, is a critical molecule involved in cancer development. However, the association between p53 Arg72Pro polymorphism and cancer risk remains unclear, possibly due to the pro-tumor potential of p53 under metabolic stress. Here, we hypothesized that the p53 Arg72Pro polymorphism plays different roles during tumorigenesis by adiposity status. We measured baseline body mass index (BMI) and p53 Arg72Pro polymorphism for two case-cohorts, which included 4264 cancers with up to 20 years of follow-up. Multivariable-adjusted hazard ratios (HRs) and confidence intervals (CIs) were estimated using weighted Cox proportional-hazards method. Without consideration of adiposity status, p53 Arg72Pro polymorphism was not associated with cancer risk. However, proline (Pro) homozygous genotype conferred an increased cancer risk for individuals with a BMI <25 kg/m

Indexed as

NeoplasmsObesityTumor Suppressor Protein p53Case-Control StudiesEast Asian PeopleGenetic Predisposition to DiseaseHumansJapanPolymorphism, Single NucleotideProspective StudiesRisk FactorsTP53 protein, humanTumor Suppressor Protein p53adipositycancergene-environment interactionp53p53 Arg72Pro polymorphism

Identifiers

PMID36083231
PMCPMC9746027
OpenAlexW4295049471

What OpenQuestion holds

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LicenceCC BY-NC
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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.