Skip to main content
Erschienen in: Tumor Biology 4/2014

01.04.2014 | Research Article

Study on the association between the Arg194Trp polymorphism in the XRCC1 gene and the risk of hematological malignancies

verfasst von: Lizhi Tang, Tianyuan Xiong, Qingyi Jia, Qing He, Xiang Tong, Yuanling Peng, Jiani Shen, Jiqiao Yang, Yonggang Zhang

Erschienen in: Tumor Biology | Ausgabe 4/2014

Einloggen, um Zugang zu erhalten

Abstract

The association between the Arg194Trp polymorphism in the XRCC1 gene and the risk of hematological malignancies has been extensively investigated. However, the results were inconsistent. The objective of the current study is to investigate the association by meta-analysis. We searched the PubMed, Embase, CNKI, Wanfang, and Weipu databases, covering all studies until Aug. 7, 2013. Statistical analysis was performed by using the RevMan4.2 software and the Stata10.0 software. A total of 20 case–control studies concerning the Arg194Trp polymorphism were indentified from 19 articles. In total analysis, our results suggested that the Arg194Trp polymorphism was not associated with an increased/decreased risk of hematological malignancies (odds ratio (OR) = 1.01, 95 % confidence interval (CI) = 0.85–1.22, P = 0.87 for Arg/Trp+Trp/Trp vs. Arg/Arg). In the subgroup analysis by ethnicity, no significant association was found either among Asians (OR = 1.04, 95 % CI = 0.84–1.29, P = 0.72) or among Europeans (OR = 1.04, 95 % CI = 0.72–1.49, P = 0.83); in the subgroup analyses by cancer types, no significant association was found either among leukemia (OR = 1.10, 95 % CI = 0.89–1.35, P = 0.39) or in lymphoma (OR = 0.83, 95 % CI = 0.57–1.22, P = 0.35). The current meta-analysis indicated that the Arg194Trp polymorphism in the XRCC1 gene might be not a risk factor for hematological malignancies. In the future, more large-scale case–control studies are needed to validate these results.
Literatur
5.
Zurück zum Zitat Simons A, Sikkema-Raddatz B, de Leeuw N, Konrad NC, Hastings RJ, Schoumans J. Genome-wide arrays in routine diagnostics of hematological malignancies. Hum Mutat. 2012;33(6):941–8. doi:10.1002/humu.22057.PubMedCrossRef Simons A, Sikkema-Raddatz B, de Leeuw N, Konrad NC, Hastings RJ, Schoumans J. Genome-wide arrays in routine diagnostics of hematological malignancies. Hum Mutat. 2012;33(6):941–8. doi:10.​1002/​humu.​22057.PubMedCrossRef
6.
Zurück zum Zitat Kroeze LI, Nikoloski G, da Silva-Coelho P, van Hoogen P, Stevens-Linders E, Kuiper RP, et al. Genetic defects in PRC2 components other than EZH2 are not common in myeloid malignancies. Blood. 2012;119(5):1318–9. doi:10.1182/blood-2011-07-365213.PubMedCrossRef Kroeze LI, Nikoloski G, da Silva-Coelho P, van Hoogen P, Stevens-Linders E, Kuiper RP, et al. Genetic defects in PRC2 components other than EZH2 are not common in myeloid malignancies. Blood. 2012;119(5):1318–9. doi:10.​1182/​blood-2011-07-365213.PubMedCrossRef
7.
Zurück zum Zitat Jagasia M, Clark WB, Brown-Gentry KD, Crawford DC, Fan KH, Chen H, et al. Genetic variation in donor CTLA-4 regulatory region is a strong predictor of outcome after allogeneic hematopoietic cell transplantation for hematologic malignancies. Biol Blood marrow Transplant J Am Soc Blood Marrow Transplant. 2012;18(7):1069–75. doi:10.1016/j.bbmt.2011.12.518.CrossRef Jagasia M, Clark WB, Brown-Gentry KD, Crawford DC, Fan KH, Chen H, et al. Genetic variation in donor CTLA-4 regulatory region is a strong predictor of outcome after allogeneic hematopoietic cell transplantation for hematologic malignancies. Biol Blood marrow Transplant J Am Soc Blood Marrow Transplant. 2012;18(7):1069–75. doi:10.​1016/​j.​bbmt.​2011.​12.​518.CrossRef
11.
Zurück zum Zitat Canalle R, Silveira VS, Scrideli CA, Queiroz RG, Lopes LF, Tone LG. Impact of thymidylate synthase promoter and DNA repair gene polymorphisms on susceptibility to childhood acute lymphoblastic leukemia. Leuk Lymphoma. 2011;52(6):1118–26. doi:10.3109/10428194.2011.559672.PubMedCrossRef Canalle R, Silveira VS, Scrideli CA, Queiroz RG, Lopes LF, Tone LG. Impact of thymidylate synthase promoter and DNA repair gene polymorphisms on susceptibility to childhood acute lymphoblastic leukemia. Leuk Lymphoma. 2011;52(6):1118–26. doi:10.​3109/​10428194.​2011.​559672.PubMedCrossRef
12.
Zurück zum Zitat Duman N, Aktan M, Ozturk S, Palanduz S, Cakiris A, Ustek D, et al. Investigation of Arg399Gln and Arg194Trp polymorphisms of the XRCC1 (x-ray cross-complementing group 1) gene and its correlation to sister chromatid exchange frequency in patients with chronic lymphocytic leukemia. Genet Test Mol Biomark. 2012;16(4):287–91. doi:10.1089/gtmb.2011.0152.CrossRef Duman N, Aktan M, Ozturk S, Palanduz S, Cakiris A, Ustek D, et al. Investigation of Arg399Gln and Arg194Trp polymorphisms of the XRCC1 (x-ray cross-complementing group 1) gene and its correlation to sister chromatid exchange frequency in patients with chronic lymphocytic leukemia. Genet Test Mol Biomark. 2012;16(4):287–91. doi:10.​1089/​gtmb.​2011.​0152.CrossRef
19.
20.
Zurück zum Zitat Baris S, Celkan T, Batar B, Guven M, Ozdil M, Ozkan A, et al. Association between genetic polymorphism in DNA repair genes and risk of B-cell lymphoma. Pediatr Hematol Oncol. 2009;26(6):467–72. doi:10.3109/08880010903096201.PubMed Baris S, Celkan T, Batar B, Guven M, Ozdil M, Ozkan A, et al. Association between genetic polymorphism in DNA repair genes and risk of B-cell lymphoma. Pediatr Hematol Oncol. 2009;26(6):467–72. doi:10.​3109/​0888001090309620​1.PubMed
22.
Zurück zum Zitat Li J. Association of XRCC1 polymorphism with leukemia susceptibility in northwest Chinese population. Lanzhou: Lanzhou University. 2011 (in press) Li J. Association of XRCC1 polymorphism with leukemia susceptibility in northwest Chinese population. Lanzhou: Lanzhou University. 2011 (in press)
24.
25.
Zurück zum Zitat Meza-Espinoza JP, Peralta-Leal V, Gutierrez-Angulo M, Macias-Gomez N, Ayala-Madrigal ML, Barros-Nunez P, et al. XRCC1 polymorphisms and haplotypes in Mexican patients with acute lymphoblastic leukemia. Genet Mol Res GMR. 2009;8(4):1451–8. doi:10.4238/vol8-4gmr687.CrossRef Meza-Espinoza JP, Peralta-Leal V, Gutierrez-Angulo M, Macias-Gomez N, Ayala-Madrigal ML, Barros-Nunez P, et al. XRCC1 polymorphisms and haplotypes in Mexican patients with acute lymphoblastic leukemia. Genet Mol Res GMR. 2009;8(4):1451–8. doi:10.​4238/​vol8-4gmr687.CrossRef
27.
Zurück zum Zitat Pakakasama S, Sirirat T, Kanchanachumpol S, Udomsubpayakul U, Mahasirimongkol S, Kitpoka P, et al. Genetic polymorphisms and haplotypes of DNA repair genes in childhood acute lymphoblastic leukemia. Pediatr Blood Cancer. 2007;48(1):16–20. doi:10.1002/pbc.20742.PubMedCrossRef Pakakasama S, Sirirat T, Kanchanachumpol S, Udomsubpayakul U, Mahasirimongkol S, Kitpoka P, et al. Genetic polymorphisms and haplotypes of DNA repair genes in childhood acute lymphoblastic leukemia. Pediatr Blood Cancer. 2007;48(1):16–20. doi:10.​1002/​pbc.​20742.PubMedCrossRef
28.
Zurück zum Zitat Shen M, Purdue MP, Kricker A, Lan Q, Grulich AE, Vajdic CM, et al. Polymorphisms in DNA repair genes and risk of non-Hodgkin’s lymphoma in New South Wales, Australia. Haematologica. 2007;92(9):1180–5.PubMedCrossRef Shen M, Purdue MP, Kricker A, Lan Q, Grulich AE, Vajdic CM, et al. Polymorphisms in DNA repair genes and risk of non-Hodgkin’s lymphoma in New South Wales, Australia. Haematologica. 2007;92(9):1180–5.PubMedCrossRef
29.
Zurück zum Zitat Shi JY, Ren ZH, Jiao B, Xiao R, Yun HY, Chen B, et al. Genetic variations of DNA repair genes and their prognostic significance in patients with acute myeloid leukemia. Int J Cancer J Int du cancer. 2011;128(1):233–8. doi:10.1002/ijc.25318.CrossRef Shi JY, Ren ZH, Jiao B, Xiao R, Yun HY, Chen B, et al. Genetic variations of DNA repair genes and their prognostic significance in patients with acute myeloid leukemia. Int J Cancer J Int du cancer. 2011;128(1):233–8. doi:10.​1002/​ijc.​25318.CrossRef
30.
Zurück zum Zitat Smedby KE, Lindgren CM, Hjalgrim H, Humphreys K, Schollkopf C, Chang ET, et al. Variation in DNA repair genes ERCC2, XRCC1, and XRCC3 and risk of follicular lymphoma. Cancer epidemiology, biomarkers & prevention: a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2006;15(2):258–65. doi:10.1158/1055-9965.EPI-05-0583.CrossRef Smedby KE, Lindgren CM, Hjalgrim H, Humphreys K, Schollkopf C, Chang ET, et al. Variation in DNA repair genes ERCC2, XRCC1, and XRCC3 and risk of follicular lymphoma. Cancer epidemiology, biomarkers & prevention: a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2006;15(2):258–65. doi:10.​1158/​1055-9965.​EPI-05-0583.CrossRef
31.
Zurück zum Zitat Zhu R, Wu Y, Lu FJ, Wang AH, Tang JY, Zhao JC, et al. Polymorphisms and haplotypes of XRCC1 and APE1 and risk of childhood leukaemia in China: a case-control analysis. Eur J Oncol. 2008;13(3):187–92. Zhu R, Wu Y, Lu FJ, Wang AH, Tang JY, Zhao JC, et al. Polymorphisms and haplotypes of XRCC1 and APE1 and risk of childhood leukaemia in China: a case-control analysis. Eur J Oncol. 2008;13(3):187–92.
32.
Metadaten
Titel
Study on the association between the Arg194Trp polymorphism in the XRCC1 gene and the risk of hematological malignancies
verfasst von
Lizhi Tang
Tianyuan Xiong
Qingyi Jia
Qing He
Xiang Tong
Yuanling Peng
Jiani Shen
Jiqiao Yang
Yonggang Zhang
Publikationsdatum
01.04.2014
Verlag
Springer Netherlands
Erschienen in
Tumor Biology / Ausgabe 4/2014
Print ISSN: 1010-4283
Elektronische ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-013-1388-5

Weitere Artikel der Ausgabe 4/2014

Tumor Biology 4/2014 Zur Ausgabe

Adjuvante Immuntherapie verlängert Leben bei RCC

25.04.2024 Nierenkarzinom Nachrichten

Nun gibt es auch Resultate zum Gesamtüberleben: Eine adjuvante Pembrolizumab-Therapie konnte in einer Phase-3-Studie das Leben von Menschen mit Nierenzellkarzinom deutlich verlängern. Die Sterberate war im Vergleich zu Placebo um 38% geringer.

Alectinib verbessert krankheitsfreies Überleben bei ALK-positivem NSCLC

25.04.2024 NSCLC Nachrichten

Das Risiko für Rezidiv oder Tod von Patienten und Patientinnen mit reseziertem ALK-positivem NSCLC ist unter einer adjuvanten Therapie mit dem Tyrosinkinase-Inhibitor Alectinib signifikant geringer als unter platinbasierter Chemotherapie.

Bei Senioren mit Prostatakarzinom auf Anämie achten!

24.04.2024 DGIM 2024 Nachrichten

Patienten, die zur Behandlung ihres Prostatakarzinoms eine Androgendeprivationstherapie erhalten, entwickeln nicht selten eine Anämie. Wer ältere Patienten internistisch mitbetreut, sollte auf diese Nebenwirkung achten.

ICI-Therapie in der Schwangerschaft wird gut toleriert

Müssen sich Schwangere einer Krebstherapie unterziehen, rufen Immuncheckpointinhibitoren offenbar nicht mehr unerwünschte Wirkungen hervor als andere Mittel gegen Krebs.

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.