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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Aug 2016.

Xeroderma pigmentosum, complementation group A

XPA, xeroderma pigmentosum complementation group A
This gene encodes a zinc finger protein involved in DNA excision repair. The encoded protein is part of the NER (nucleotide excision repair) complext which is responsible for repair of UV radiation-induced photoproducts and DNA adducts induced by chemical carcinogens. Mutations in this gene are associated with xeroderma pigmentosum complementation group A. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2009] (from NCBI)
Top mentioned proteins: XPC, CAN, ERCC1, XPG, XPD
Papers on XPA
Association of nucleotide excision repair pathway gene polymorphisms with gastric cancer and atrophic gastritis risks.
Yuan et al., Shenyang, China. In Oncotarget, Feb 2016
XPA rs2808668 and drinking, DDB2 rs326222, rs3781619, rs830083 and smoking demonstrated significant interactions in AG; XPC rs2607775 had significant interaction with smoking in GC.
Base and Nucleotide Excision Repair of Oxidatively Generated Guanine Lesions in DNA.
Geacintov et al., New York City, United States. In J Biol Chem, Feb 2016
The ladders were not observed when NER was inhibited either by mouse monoclonal antibody [5F12] to human XPA, or in XPC(-/-) fibroblast cell extracts.
Covalent DNA-Protein Cross-linking by Phosphoramide Mustard and Nornitrogen Mustard in Human Cells.
Tretyakova et al., In Chem Res Toxicol, Jan 2016
Cys-NOR-N7G adduct numbers were higher in NER-deficient Xeroderma pigmentosum cells (XPA) as compared with repair proficient cells.
TP53 and lacZ mutagenesis induced by 3-nitrobenzanthrone in Xpa-deficient human TP53 knock-in mouse embryo fibroblasts.
Arlt et al., London, United Kingdom. In Dna Repair (amst), Jan 2016
To this end we utilised Xpa -knockout (Xpa-Null) human TP53 knock-in (Hupki) embryo fibroblasts (HUFs).
The ERCC1 and ERCC4 (XPF) genes and gene products.
Wood et al., United States. In Gene, Oct 2015
ERCC1-XPF interacts with other proteins including XPA, RPA, SLX4 and TRF2 to perform its functions.
Xeroderma pigmentosa: three new cases with an in depth review of the genetic and clinical characteristics of the disease.
Shehata et al., Atlanta, United States. In Fetal Pediatr Pathol, Apr 2015
Seven genes (XPA-XPG) have a defect in Nucletoide Excision Repair (NER), while the eighth gene XPV has a defect in polymerase η, which is responsible for replication of UV-damaged DNA to produce corrected daughter strands.
Overview of xeroderma pigmentosum proteins architecture, mutations and post-translational modifications.
Bonatto et al., Porto Alegre, Brazil. In Mutat Res Rev Mutat Res, 2015
The xeroderma pigmentosum complementation group proteins (XPs), which include XPA through XPG, play a critical role in coordinating and promoting global genome and transcription-coupled nucleotide excision repair (GG-NER and TC-NER, respectively) pathways in eukaryotic cells.
Defective mitophagy in XPA via PARP-1 hyperactivation and NAD(+)/SIRT1 reduction.
Bohr et al., Baltimore, United States. In Cell, 2014
We identify mitochondrial dysfunction in xeroderma pigmentosum group A (XPA), a nucleotide excision DNA repair disorder with severe neurodegeneration, in silico and in vivo.
Polymorphisms in DNA repair genes of XRCC1, XPA, XPC, XPD and associations with lung cancer risk in Chinese people.
Zhou et al., Tianjin, China. In Thorac Cancer, 2014
RESULTS: In single tag SNP analysis, XPA rs2808668, XPC rs2733533, and XPD rs1799787 were significantly associated with lung cancer susceptibility.
Cadmium and cancer.
Hartwig, Karlsruhe, Germany. In Met Ions Life Sci, 2012
Particularly sensitive targets appear to be proteins with zinc-binding structures, present in DNA repair proteins such as XPA, PARP-1 as well as in the tumor suppressor protein p53.
XPA A23G polymorphism and susceptibility to cancer: a meta-analysis.
Pan et al., Jinan, China. In Mol Biol Rep, 2012
The XPA A23G G allele is a low-penetrant risk factor for cancer development. [Meta-analysis]
Delayed neuromotor recovery and increased memory acquisition dysfunction following experimental brain trauma in mice lacking the DNA repair gene XPA.
McIntosh et al., Lund, Sweden. In J Neurosurg, 2012
The authors' results suggest that lack of the DNA repair factor XPA may delay neurobehavioral recovery after TBI
HIF1α regulated expression of XPA contributes to cisplatin resistance in lung cancer.
Belinsky et al., Albuquerque, United States. In Carcinogenesis, 2012
studies identify HIF1alpha as a key protein in regulating transcription of XPA in lung cancer cell lines and primary tumors contributing to cisplatin resistance
Platelet-activating factor receptor agonists mediate xeroderma pigmentosum A photosensitivity.
Travers et al., Indianapolis, United States. In J Biol Chem, 2012
Oxidized glycerophosphocholines play a pivotal role in the photosensitivity associated with the deficiency of XPA.
DNA-damage accumulation and replicative arrest in Hutchinson-Gilford progeria syndrome.
Zou et al., Johnson City, United States. In Biochem Soc Trans, 2011
We propose that progerin accumulation results in disruption of functions of some replication and repair factors, causing the mislocalization of XPA (xeroderma pigmentosum group A) protein to the replication forks, replication fork stalling and, subsequently, DNA DSBs.
[The relationship between polymorphism of genes XPA, XPC, XPD, XRCC1 and susceptibility to acute lymphoblastic leukemia].
Xu et al., Nanjing, China. In Zhonghua Nei Ke Za Zhi, 2011
XPA A23G and XPC C499T polymorphisms may contribute to the risk of developing acute lymphoblastic leukemia.
Pharmacogenetic analyses of a phase III trial in metastatic gastroesophageal adenocarcinoma with fluorouracil and leucovorin plus either oxaliplatin or cisplatin: a study of the arbeitsgemeinschaft internistische onkologie.
Stoehlmacher et al., Dresden, Germany. In J Clin Oncol, 2009
Polymorphisms within genes of TS, MTHFR, MTR, OPRT, XPD, ERCC1, XRCC1, XPA, GSTP1, GSTT1, and GSTM1 were genotyped using polymerase chain reaction-based techniques.
Premature aging in mice deficient in DNA repair and transcription.
Hoeijmakers et al., Rotterdam, Netherlands. In Science, 2002
TTD mice carrying an additional mutation in XPA, which enhances the DNA repair defect, showed a greatly accelerated aging phenotype, which correlated with an increased cellular sensitivity to oxidative DNA damage.
Antiproliferative activity of ecteinascidin 743 is dependent upon transcription-coupled nucleotide-excision repair.
Pommier et al., Bethesda, United States. In Nat Med, 2001
Xeroderma pigmentosum cells deficient in the NER genes XPG, XPA, XPD or XPF were resistant to Et743, and sensitivity was restored by complementation with wild-type genes.
Structural basis for the recognition of DNA repair proteins UNG2, XPA, and RAD52 by replication factor RPA.
Chazin et al., Los Angeles, United States. In Cell, 2000
We have shown that a globular domain at the C terminus of subunit RPA32 contains a specific surface that interacts in a similar manner with the DNA repair enzyme UNG2 and repair factors XPA and RAD52, each of which functions in a different repair pathway.
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