Polymorphisms in DNA repair genes and risk of non-hodgkin lymphoma in a pooled analysis of three studies

British Journal of Haematology

Volumn 151, Issue 3, 2010, Pages 239-244

  Shen, Min ^a   Menashe, Idan ^a   Morton, Lindsay M ^a   Zhang, Yawei ^b   Armstrong, Bruce ^c   Wang, Sophia S ^a   Lan, Qing ^a   Hartge, Patricia ^a   Purdue, Mark P ^a   Cerhan, James R ^d   Grulich, Andrew ^e   Cozen, Wendy ^f   Yeager, Meredith ^a   Holford, Theodore R ^b   Vajdic, Claire M ^g   Davis, Scott ^h   Leaderer, Brian ^b   Kricker, Anne ^c   Severson, Richard K ⁱ   Zahm, Shelia H ^a   Chatterjee, Nilanjan ^a   Rothman, Nathaniel ^a   Chanock, Stephen J ^a   Zheng, Tongzhang ^b   more..

^a NATIONAL CANCER INSTITUTE   (United States)

^b YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF SYDNEY   (Australia)

^d MAYO CLINIC   (United States)

^e UNIVERSITY OF NEW SOUTH WALES   (Australia)

^f UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^g UNIVERSITY OF NEW SOUTH WALES   (Australia)

^h Fred Hutchinson Cancer Research Center   (United States)

ⁱ WAYNE STATE UNIVERSITY   (United States)

Author keywords

DNA repair; Non hodgkin lymphoma; pooled analysis; single nucleotide polymorphism

Indexed keywords

BLOOM SYNDROME HELICASE; RAD50 PROTEIN; XRCC4 PROTEIN; DNA;

ARTICLE; AUSTRALIA; BLM GENE; CANCER RISK; CHRONIC LYMPHATIC LEUKEMIA; DNA REPAIR; DOUBLE STRANDED DNA BREAK; ERCC3 GENE; EXCISION REPAIR; FAM82A2 GENE; FOLLICULAR LYMPHOMA; GENETIC RISK; GENOTYPE; HUMAN; LARGE CELL LYMPHOMA; MARGINAL ZONE LYMPHOMA; NONHODGKIN LYMPHOMA; POPULATION BASED CASE CONTROL STUDY; PRIORITY JOURNAL; RAD50 GENE; SINGLE NUCLEOTIDE POLYMORPHISM; SMALL LYMPHOCYTIC LYMPHOMA; UNITED STATES; XRCC4 GENE; ADULT; AGED; CASE CONTROL STUDY; FEMALE; GENETIC PREDISPOSITION; GENETICS; MALE; META ANALYSIS; MIDDLE AGED;

ADULT; AGED; CASE-CONTROL STUDIES; DNA REPAIR; DNA, NEOPLASM; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; LYMPHOMA, NON-HODGKIN; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 78651468484     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2010.08364.x     Document Type: Article

References (14)

1. Chen, B.E., Sakoda, L.C., Hsing, A.W. & Rosenberg, P.S. (2006) Resampling-based multiple hypothesis testing procedures for genetic case-control association studies. Genetic Epidemiology, 30, 495-507.
2. Gao, Y., Ferguson, D.O., Xie, W., Manis, J.P., Sekiguchi, J., Frank, K.M., Chaudhuri, J., Horner, J., DePinho, R.A. & Alt, F.W. (2000) Interplay of p53 and DNA-repair protein XRCC4 in tumorigenesis, genomic stability and development. Nature, 404, 897-900.
3. Hill, D.A., Wang, S.S., Cerhan, J.R., Davis, S., Cozen, W., Severson, R.K., Hartge, P., Wacholder, S., Yeager, M., Chanock, S.J. & Rothman, N. (2006) Risk of non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair and related genes. Blood, 108, 3161-3167.
4. Jaffe, E.S. (ed.) (2001) Pathology and Genetics of Tumours of Haematopoietic and Lymphoid Tissues. International Agency for Research on Cancer (IARC) Press, Lyon, France.
5. Kaneko, H. & Kondo, N. (2004) Clinical features of Bloom syndrome and function of the causative gene, BLM helicase. Expert Review of Molecular Diagnostics, 4, 393-401.
6. Lv, B.F., Yu, C.F., Chen, Y.Y., Lu, Y., Guo, J.H., Song, Q.S., Ma, D.L., Shi, T.P. & Wang, L. (2006) Protein tyrosine phosphatase interacting protein 51 (PTPIP51) is a novel mitochondria protein with an N-terminal mitochondrial targeting sequence and induces apoptosis. Apoptosis, 11, 1489-1501.
7. Morton, L.M., Turner, J.J., Cerhan, J.R., Linet, M.S., Treseler, P.A., Clarke, C.A., Jack, A., Cozen, W., Maynadie, M., Spinelli, J.J., Costantini, A.S., Rudiger, T., Scarpa, A., Zheng, T. & Weisenburger, D.D. (2007) Proposed classification of lymphoid neoplasms for epidemiologic research from the Pathology Working Group of the International Lymphoma Epidemiology Consortium (InterLymph). Blood, 110, 695-708.
8. Palitti, F. (2004) Mechanisms of formation of chromosomal aberrations: insights from studies with DNA repair-deficient cells. Cytogenetic and Genome Research, 104, 95-99.
9. Shen, M., Zheng, T., Lan, Q., Zhang, Y., Zahm, S.H., Wang, S.S., Holford, T.R., Leaderer, B., Yeager, M., Welch, R., Kang, D., Boyle, P., Zhang, B., Zou, K., Zhu, Y., Chanock, S. & Rothman, N. (2006) Polymorphisms in DNA repair genes and risk of non-Hodgkin lymphoma among women in Connecticut. Human Genetics, 119, 659-668.
10. Shen, M., Purdue, M.P., Kricker, A., Lan, Q., Grulich, A.E., Vajdic, C.M., Turner, J., Whitby, D., Chanock, S., Rothman, N. & Armstrong, B.K. (2007) Polymorphisms in DNA repair genes and risk of non-Hodgkin's lymphoma in New South Wales, Australia. Haematologica, 92, 1180-1185.
11. Sibanda, B.L., Critchlow, S.E., Begun, J., Pei, X.Y., Jackson, S.P., Blundell, T.L. & Pellegrini, L. (2001) Crystal structure of an Xrcc4-DNA ligase IV complex. Nature Structural Biology, 8, 1015-1019.
12. So, S., Adachi, N., Lieber, M.R. & Koyama, H. (2004) Genetic interactions between BLM and DNA ligase IV in human cells. Journal of Biological Chemistry, 279, 55433-55442.
13. Taylor, J. & Tibshirani, R. (2006) A tail strength measure for assessing the overall univariate significance in a dataset. Biostatistics, 7, 167-181.
14. Thacker, J. (2005) The RAD51 gene family, genetic instability and cancer. Cancer Letters, 219, 125-135.