Literature DB >> 23330005

Expression of XPG protein in human normal and tumor tissues.

Miguel Aracil1, Lisa M Dauffenbach, Marta Martínez Diez, Rana Richeh, Victoria Moneo, Juan Fernando Martínez Leal, Luis Francisco García Fernández, Christopher A Kerfoot, Carlos M Galmarini.   

Abstract

XPG (Xeroderma pigmentosum group G complementing factor) is a protein associated with DNA repair and transcription. Point mutations in ERCC5, the gene coding for XPG, cause the cancer-prone disorder xeroderma pigmentosum (XP) while truncation mutations give rise to individuals with the combined clinical features of XP and Cockayne syndrome. Polymorphisms of ERCC5 or alterations in XPG mRNA expression were also associated to an increase risk of different cancers types and to prognosis of cancer patients. However, the expression of XPG protein in different normal or tumor human tissues is not well known. In the present work, we have validated an immunohistochemistry (IHC) assay for detection of expression levels of XPG protein in FFPE human tissue samples. We have also tested this IHC assay in different normal and tumor human tissues. On a microarray containing 28 normal cores, positive staining was observed in 60% of the samples. The highest staining was detected in adrenal gland, breast, colon, heart, kidney, thyroid and tongue. In tumors, positive staining was observed in 9 of 10 breast cancer samples and in all 5 ovarian cancer and 5 sarcomas samples. Subcellular localization was predominantly nuclear. The use of this validated methodology would help to interpret the role of XPG in tumorogenesis and its use as a possible prognostic or predictive factor.

Entities:  

Keywords:  XPG; immunohistochemistry; tumor tissue

Mesh:

Substances:

Year:  2013        PMID: 23330005      PMCID: PMC3544242     

Source DB:  PubMed          Journal:  Int J Clin Exp Pathol        ISSN: 1936-2625


  44 in total

1.  Structural determinants for substrate binding and catalysis by the structure-specific endonuclease XPG.

Authors:  Marcel Hohl; Fabrizio Thorel; Stuart G Clarkson; Orlando D Schärer
Journal:  J Biol Chem       Date:  2003-03-18       Impact factor: 5.157

Review 2.  Xeroderma pigmentosum/cockayne syndrome complex: first neuropathological study and review of eight other cases.

Authors:  Y Lindenbaum; D Dickson; P Rosenbaum; K Kraemer; I Robbins; I Rapin
Journal:  Eur J Paediatr Neurol       Date:  2001       Impact factor: 3.140

Review 3.  Xeroderma pigmentosum and related disorders: defects in DNA repair and transcription.

Authors:  M Berneburg; A R Lehmann
Journal:  Adv Genet       Date:  2001       Impact factor: 1.944

4.  Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5.

Authors:  A O'Donovan; R D Wood
Journal:  Nature       Date:  1993-05-13       Impact factor: 49.962

Review 5.  XPG: its products and biological roles.

Authors:  Orlando D Schärer
Journal:  Adv Exp Med Biol       Date:  2008       Impact factor: 2.622

6.  Relationship between XPG codon 1104 polymorphism and risk of primary lung cancer.

Authors:  Hyo-Sung Jeon; Kyung Mee Kim; Sun Ha Park; Su Yeon Lee; Jin Eun Choi; Ga Young Lee; Sin Kam; Rang Woon Park; In-San Kim; Chang Ho Kim; Tae Hoon Jung; Jae Yong Park
Journal:  Carcinogenesis       Date:  2003-07-17       Impact factor: 4.944

Review 7.  DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy.

Authors:  Alan R Lehmann
Journal:  Biochimie       Date:  2003-11       Impact factor: 4.079

Review 8.  The eukaryotic nucleotide excision repair pathway.

Authors:  Renata M A Costa; Vanessa Chiganças; Rodrigo da Silva Galhardo; Helotonio Carvalho; Carlos F M Menck
Journal:  Biochimie       Date:  2003-11       Impact factor: 4.079

9.  Requirement of yeast RAD2, a homolog of human XPG gene, for efficient RNA polymerase II transcription. implications for Cockayne syndrome.

Authors:  Sung-Keun Lee; Sung-Lim Yu; Louise Prakash; Satya Prakash
Journal:  Cell       Date:  2002-06-28       Impact factor: 41.582

10.  Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients.

Authors:  Steffen Emmert; Hanoch Slor; David B Busch; Sima Batko; Roberta B Albert; Donna Coleman; Sikandar G Khan; Bassam Abu-Libdeh; John J DiGiovanna; Bari B Cunningham; Myung-Moo Lee; Jill Crollick; Hiroki Inui; Takahiro Ueda; Mohammad Hedayati; Lawrence Grossman; Tala Shahlavi; James E Cleaver; Kenneth H Kraemer
Journal:  J Invest Dermatol       Date:  2002-06       Impact factor: 8.551

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  4 in total

1.  Elucidation of Increased Cervical Cancer Risk Due to Polymorphisms in XRCC1 (R399Q and R194W), ERCC5 (D1104H), and NQO1 (P187S).

Authors:  Shrishty Tyagi; Nisha Chaudhary; Agneesh Pratim Das; Sandeep Saini; Subhash Mohan Agarwal
Journal:  Reprod Sci       Date:  2022-10-04       Impact factor: 2.924

2.  Expression of XPG protein in the development, progression and prognosis of gastric cancer.

Authors:  Na Deng; Jing-wei Liu; Li-ping Sun; Qian Xu; Zhi-Peng Duan; Nan-Nan Dong; Yuan Yuan
Journal:  PLoS One       Date:  2014-09-30       Impact factor: 3.240

3.  Identification of a Splenic Marginal Zone Lymphoma Signature: Preliminary Findings With Diagnostic Potential.

Authors:  Jacob E Robinson; Timothy C Greiner; Alyssa C Bouska; Javeed Iqbal; Christine E Cutucache
Journal:  Front Oncol       Date:  2020-05-08       Impact factor: 6.244

4.  Splice variants of the endonucleases XPF and XPG contain residual DNA repair capabilities and could be a valuable tool for personalized medicine.

Authors:  Janin Lehmann; Steffen Schubert; Christina Seebode; Antje Apel; Andreas Ohlenbusch; Steffen Emmert
Journal:  Oncotarget       Date:  2017-12-08
  4 in total

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