Evidence map›Paper›PMID 15107491›Full record

ArticleNucleic acids research2004

The initiative role of XPC protein in cisplatin DNA damaging treatment-mediated cell cycle regulation.

Gan Wang, Lynn Chuang, Xiaohong Zhang, Stephanie Colton, Alan Dombkowski, John Reiners, Amy Diakiw, Xiaoxin Susan Xu

Open access · bronzeAbstract read
In one paragraph

Article in Nucleic acids research, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 19% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

  1. Associations between polymorphisms of the XPC gene and lung cancer susceptibility: a meta-analysis.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Pooled it
  2. Article
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  4. Review
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  6. TheHeliyon · 2021
    Article
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  8. Effect ofOncoTargets and therapy · 2019
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  20. Effect of eIF3a on response of lung cancer patients to platinum-based chemotherapy by regulating DNA repair.Clinical cancer research : an official journal of the American Association for Cancer Research · 2011
    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 at 1 institution in 1 country.

Gan WangInstitute of Environmental Health Sciences, Wayne State University, 2727 Second Avenue, Room 4325, Detroit, MI 48201, USA. g.wang@wayne.edu
Lynn Chuang
Xiaohong Zhang
Stephanie Colton
Alan Dombkowski
John Reiners
Amy Diakiw
Xiaoxin Susan Xu
Wayne State University · US

Funding

RESEARCH CORE-- SIGNAL TRANSDUCTIONP30ES006639 · NIEHS · WAYNE STATE UNIVERSITY · PI DERESKI, MARY O · 1994 to 2008
$13.1M
TRANCRIPTION-COUPLED DNA REPAIR AND GENETIC INSTABILITYR01ES009699 · NIEHS · WAYNE STATE UNIVERSITY · PI WANG, GAN · 2000 to 2004
$1.1M
NIEHS NIH HHS P30 ES006639NIEHS NIH HHS P30 ES06639NIEHS NIH HHS R01 ES009699NIEHS NIH HHS R01ES09699
6 · The paper itself

Abstract

XPC is an important DNA damage recognition protein involved in DNA nucleotide excision repair. We have studied the role of the XPC protein in cisplatin treatment-mediated cell cycle regulation. Through the comparison of microarray data obtained from human normal fibroblasts and two individual XPC-defective cell lines, 486 genes were identified as XPC-responsive genes in the cisplatin treatment (with a minimal 1.5-fold change) and 297 of these genes were further mapped to biological pathways and gene ontologies. The cell cycle and cell proliferation-related genes were the most affected genes by the XPC defect in the cisplatin treatment. Many other cellular function genes were also affected by the XPC defect in the treatment. Western blot hybridization results revealed that the XPC defect reduced the p53 responses to the cisplatin treatment. The ability to activate caspase-3 was also attenuated in the XPC cells with the treatment. These results suggest that the XPC protein plays a critical role in initiating the cisplatin DNA damaging treatment-mediated signal transduction process, resulting in activation of the p53 pathway and cell cycle arrest that allow DNA repair and apoptosis to take place. These results reveal an important role of the XPC protein in the cancer prevention.

Indexed as

ApoptosisCaspase 3CaspasesCell CycleCell LineCisplatinCyclin-Dependent Kinase Inhibitor p21CyclinsDNA-Binding ProteinsDNA DamageDNA RepairEnzyme ActivationGene Expression ProfilingGene Expression RegulationGenes, cdcHumansCASP3 protein, humanCaspase 3CaspasesCDKN1A protein, humanCisplatinCyclin-Dependent Kinase Inhibitor p21CyclinsDNA-Binding ProteinsRNA, MessengerTumor Suppressor Protein p53XPC protein, human

Identifiers

PMID15107491
PMCPMC407824
OpenAlexW2082054147

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.