Evidence map›Paper›PMID 21621504›Full record

ArticleArchives of biochemistry and biophysics2011

Upregulation of the mitochondrial transport protein, Tim50, by mutant p53 contributes to cell growth and chemoresistance.

Heidi Sankala, Catherine Vaughan, Jing Wang, Sumitra Deb, Paul R Graves

Abstract read
In one paragraph

Article in Archives of biochemistry and biophysics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Proteogenomic Analysis of Surgically Resected Lung Adenocarcinoma.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2018
    Article
  10. Review
  11. Article
  12. Article
  13. The consequence of oncomorphic TP53 mutations in ovarian cancer.International journal of molecular sciences · 2013
    Review
  14. Article
  15. Mutant p53: one name, many proteins.Genes & development · 2012
    Review
  16. Article
  17. 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

5 authors at 1 institution in 1 country.

Heidi SankalaDepartment of Radiation Oncology, Massey Cancer Center, Virginia Commonwealth University, Richmond, VA 23298-0058, USA.
Catherine Vaughan
Jing Wang
Sumitra Deb
Paul R Graves
Virginia Commonwealth University · US

Funding

POSTDOCTORAL TRAINING PROGRAM IN CANCER BIOLOGYT32CA085159 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI GINDER, GORDON D · 2000 to 2011
$2.0M
Chemoresistance and Motility: Role of Mutant p53 and NF-kB2 in CancerR01CA121144 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI DEB, SUMITRA · 2008 to 2011
$1.0M
BREAST CANCER ETIOLOGY--P53 GAIN OF FUNCTION MUTATIONSR01CA070712 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI DEB, SUMITRA · 1996 to 2000
$223k
NCI NIH HHS CA121144NCI NIH HHS CA70712NCI NIH HHS R01 CA070712NCI NIH HHS R01 CA121144NCI NIH HHS T32 CA085159NCI NIH HHS T32-CA085159-7
6 · The paper itself

Abstract

The p53 gene is one of the most frequently mutated genes in human cancer. Some p53 mutations impart additional functions that promote oncogenesis. To investigate how these p53 mutants function, a proteomic analysis was performed. The protein, translocator of the inner mitochondrial membrane 50 (Tim50), was upregulated in a non-small cell lung carcinoma cell line (H1299) that expressed the p53 mutants R175H and R273H compared to cells lacking p53. Tim50 was also elevated in the breast cancer cell lines MDA-MB-468 and SK-BR-3, that endogenously express the p53 mutants R175H and R273H, respectively, compared to MCF-10A. The p53 mutants R175H and R273H, but not WT p53, upregulated the expression of a Tim50 promoter construct and chromatin immunoprecipitation (ChIP) analysis indicated increased histone acetylation and increased interaction of the transcription factors Ets-1, CREB and CREB-binding protein (CBP) with the Tim50 promoter in the presence of mutant p53. Finally, reduction of Tim50 expression reduced the growth rate and chemoresistance of cells harboring mutant p53 but had no effect upon cells lacking p53. Taken together, these findings identify the Tim50 gene as a transcriptional target of mutant p53 and suggest a novel mechanism by which p53 mutants enhance cell growth and chemoresistance.

Indexed as

Gene Expression Regulation, NeoplasticMutationBreast NeoplasmsCarcinoma, Non-Small-Cell LungCell Line, TumorCell ProliferationFemaleHumansLung NeoplasmsMembrane Transport ProteinsMitochondriaMitochondrial Precursor Protein Import Complex ProteinsNeoplasmsTumor Suppressor Protein p53Up-RegulationMembrane Transport ProteinsMitochondrial Precursor Protein Import Complex ProteinsTIMM50 protein, humanTumor Suppressor Protein p53

Identifiers

PMID21621504
PMCPMC3129659
OpenAlexW2053972778

What OpenQuestion holds

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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.