Family studies in chronic lymphocytic leukaemia and other lymphoproliferative tumours

British Journal of Haematology

Volumn 139, Issue 5, 2007, Pages 774-779

  Goldin, Lynn R ^a   Caporaso, Neil E ^a  

^a NATIONAL CANCER INSTITUTE   (United States)

Author keywords

Candidate genes; Chronic lymphocytic leukaemia; Familial aggregation; Familial linkage; Susceptibility genes

Indexed keywords

ARTICLE; B LYMPHOCYTE; CASE CONTROL STUDY; CHRONIC LYMPHATIC LEUKEMIA; CLINICAL ASSESSMENT; COHORT ANALYSIS; FAMILIAL DISEASE; FAMILY STUDY; GENE IDENTIFICATION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC SCREENING; GENETIC SUSCEPTIBILITY; HIGH RISK POPULATION; HODGKIN DISEASE; HUMAN; IMMUNITY; LYMPHOCYTOSIS; LYMPHOPROLIFERATIVE DISEASE; MONOCLONAL B CELL LYMPHOCYTOSIS; MULTIPLE MYELOMA; NONHODGKIN LYMPHOMA; POPULATION RESEARCH; PRIORITY JOURNAL;

GENES, NEOPLASM; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LEUKEMIA, LYMPHOCYTIC, CHRONIC, B-CELL; LYMPHOPROLIFERATIVE DISORDERS; PEDIGREE;

EID: 36148999479     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2007.06810.x     Document Type: Article

References (48)

1. Calin, G.A., Ferracin, M., Cimmino, A., Di Leva, G., Shimizu, M., Wojcik, S.E., Iorio, M.V., Visone, R., Sever, N.I., Fabbri, M., Iuliano, R., Palumbo, T., Pichiorri, F., Roldo, C., Garzon, R., Sevignani, C., Rassenti, L., Alder, H., Volinia, S., Liu, C.G., Kipps, T.J., Negrini, M. Croce, C.M. (2005) A MicroRNA signature associated with prognosis and progression in chronic lymphocytic leukemia. New England Journal of Medicine, 353, 1793 1801.
2. Caporaso, N., Marti, G.E. Goldin, L. (2004) Perspectives on familial chronic lymphocytic leukemia: genes and the environment. Seminars in Hematology, 41, 201 206.
3. 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.
4. Cordano, P., Lake, A., Shield, L., Taylor, G.M., Alexander, F.E., Taylor, P.R., White, J. Jarrett, R.F. (2005) Effect of IL-6 promoter polymorphism on incidence and outcome in Hodgkin's lymphoma. British Journal of Haematology, 128, 493 495.
5. Cozen, W., Gill, P.S., Ingles, S.A., Masood, R., Martinez-Maza, O., Cockburn, M.G., Gauderman, W.J., Pike, M.C., Bernstein, L., Nathwani, B.N., Salam, M.T., Danley, K.L., Wang, W., Gage, J., Gundell-Miller, S. Mack, T.M. (2004) IL-6 levels and genotype are associated with risk of young adult Hodgkin lymphoma. Blood, 103, 3216 3221.
6. Daugherty, S.E., Pfeiffer, R.M., Mellemkjaer, L., Hemminki, K. Goldin, L.R. (2005) No evidence for anticipation in lymphoproliferative tumors in population-based samples. Cancer Epidemiology, Biomarkers and Prevention, 14, 1245 1250.
7. Fraumeni, Jr., J.F., Vogel, C.L. DeVita, V.T. (1969) Familial chronic lymphocytic leukemia. Annals of Internal Medicine, 71, 279 284.
8. Ghia, P., Prato, G., Scielzo, C., Stella, S., Geuna, M., Guida, G. Caligaris-Cappio, F. (2004) Monoclonal CD5+ and CD5- B-lymphocyte expansions are frequent in the peripheral blood of the elderly. Blood, 103, 2337 2342.
9. Goldin, L.R., Sgambati, M., Marti, G.E., Fontaine, L., Ishibe, N. Caporaso, N. (1999) Anticipation in familial chronic lymphocytic leukemia. American Journal of Human Genetics, 65, 265 269.
10. Goldin, L.R., Ishibe, N., Sgambati, M., Marti, G.E., Fontaine, L., Lee, M.P., Kelley, J.M., Scherpbier, T., Buetow, K.H. Caporaso, N.E. (2003) A genome scan of 18 families with chronic lymphocytic leukaemia. British Journal of Haematology, 121, 866 873.
11. Goldin, L.R., Pfeiffer, R.M., Gridley, G., Gail, M.H., Li, X., Mellemkjaer, L., Olsen, J.H., Hemminki, K. Linet, M.S. (2004a) Familial aggregation of Hodgkin lymphoma and related tumors. Cancer, 100, 1902 1908.
12. Goldin, L.R., Pfeiffer, R.M., Li, X. Hemminki, K. (2004b) Familial risk of lymphoproliferative tumors in families of patients with chronic lymphocytic leukemia: results from the Swedish Family-Cancer Database. Blood, 104, 1850 1854.
13. Goldin, L.R., Landgren, O., McMaster, M.L., Gridley, G., Hemminki, K., Li, X., Mellemkjaer, L., Olsen, J.H. Linet, M.S. (2005a) Familial aggregation and heterogeneity of non-Hodgkin lymphoma in population-based samples. Cancer Epidemiology, Biomarkers and Prevention, 14, 2402 2406.
14. Goldin, L.R., McMaster, M.L., Ter-Minassian, M., Saddlemire, S., Harmsen, B., Lalonde, G. Tucker, M.A. (2005b) A genome screen of families at high risk for Hodgkin lymphoma: evidence for a susceptibility gene on chromosome 4. Journal of Medical Genetics, 42, 595 601.
15. Houlston, R.S. Peto, J. (2004) The search for low-penetrance cancer susceptibility alleles. Oncogene, 23, 6471 6476.
16. Ishibe, N., Sgambati, M.T., Fontaine, L., Goldin, L.R., Jain, N., Weissman, N., Marti, G.E. Caporaso, N.E. (2001) Clinical characteristics of familial B-CLL in the National Cancer Institute Familial Registry. Leukemia & Lymphoma, 42, 99 108.
17. Ishibe, N., Prieto, D., Hosack, D.A., Lempicki, R.A., Goldin, L.R., Raffeld, M., Marti, G.E. Caporaso, N.E. (2002a) Telomere length and heavy-chain mutation status in familial chronic lymphocytic leukemia. Leukemia Research, 26, 791 794.
18. Ishibe, N., Albitar, M., Jilani, I.B., Goldin, L.R., Marti, G.E. Caporaso, N.E. (2002b) CXCR4 expression is associated with survival in familial chronic lymphocytic leukemia, but CD38 expression is not. Blood, 100, 1100 1101.
19. Jaffe, E.S., Harris, N.L., Stein, H. Vardiman, J.W., eds. (2001) Pathology and genetics of tumours of haematopoietic and lymphoid tissues. IARC Press, Lyon.
20. Lan, Q., Zheng, T., Rothman, N., Zhang, Y., Wang, S.S., Shen, M., Berndt, S.I., Zahm, S.H., Holford, T.R., Leaderer, B., Yeager, M., Welch, R., Boyle, P., Zhang, B., Zou, K., Zhu, Y. Chanock, S. (2006) Cytokine polymorphisms in the Th1/Th2 pathway and susceptibility to non-Hodgkin lymphoma. Blood, 107, 4101 4108.
21. Landgren, O., Linet, M.S., McMaster, M.L., Gridley, G., Hemminki, K. Goldin, L.R. (2006a) Familial characteristics of autoimmune and hematologic disorders in 8,406 multiple myeloma patients: a population-based case-control study. International Journal of Cancer, 118, 3095 3098.
22. Landgren, O., Engels, E.A., Caporaso, N.E., Gridley, G., Mellemkjaer, L., Hemminki, K., Linet, M.S. Goldin, L.R. (2006b) Patterns of autoimmunity and subsequent chronic lymphocytic leukemia in Nordic countries. Blood, 108, 292 296.
23. Lesnick, T.G., Papapetropoulos, S., Mash, D.C., Ffrench-Mullen, J., Shehadeh, L., de Andrade, M., Henley, J.R., Rocca, W.A., Ahlskog, J.E. Maraganore, D.M. (2007) A genomic pathway approach to a complex disease: axon guidance and parkinson disease. PLoS Genetics, 3, e98.
24. Marti, G.E., Carter, P., Abbasi, F., Washington, G.C., Jain, N., Zenger, V.E., Ishibe, N., Goldin, L., Fontaine, L., Weissman, N., Sgambati, M., Fauget, G., Bertin, P., Vogt, Jr., R.F., Slade, B., Noguchi, P.D., Stetler-Stevenson, M.A. Caporaso, N. (2003) B-cell monoclonal lymphocytosis and B-cell abnormalities in the setting of familial B-cell chronic lymphocytic leukemia. Cytometry Part B Clinical Cytometry, 52, 1 12.
25. Mauro, F.R., Giammartini, E., Gentile, M., Sperduti, I., Valle, V., Pizzuti, A., Guarini, A., Giannarelli, D. Foa, R. (2006) Clinical features and outcome of familial chronic lymphocytic leukemia. Haematologica, 91, 1117 1120.
26. McMaster, M.L., Goldin, L.R., Bai, Y., Ter-Minassian, M., Boehringer, S., Giambarresi, T.R., Vasquez, L.G. Tucker, M.A. (2006) Genomewide linkage screen for Waldenstrom macroglobulinemia susceptibility loci in high-risk families. American Journal of Human Genetics, 79, 695 701.
27. Ng, D., Marti, G.E., Fontaine, L., Toro, J.R., Caporaso, N. Goldin, L.R. (2006) High-density mapping and follow-up studies on chromosomal regions 1, 3, 6, 12, 13 and 17 in 28 families with chronic lymphocytic leukaemia. British Journal of Haematology, 133, 59 61.
28. Ng, D., Toure, O., Wei, M.H., Arthur, D.C., Abbasi, F., Fontaine, L., Marti, G.E., Fraumeni, Jr., J.F., Goldin, L.R., Caporaso, N. Toro, J.R. (2007) Identification of a novel chromosome region, 13q21.33-q22.2, for susceptibility genes in familial chronic lymphocytic leukemia. Blood, 109, 916 925.
29. Novak, A.J., Grote, D.M., Ziesmer, S.C., Kline, M.P., Manske, M.K., Slager, S., Witzig, T.E., Shanafelt, T., Call, T.G., Kay, N.E., Jelinek, D.F., Cerhan, J.R., Gross, J.A., Harder, B., Dillon, S.R. Ansell, S.M. (2006) Elevated serum B-lymphocyte stimulator levels in patients with familial lymphoproliferative disorders. Journal of Clinical Oncology, 24, 983 987.
30. Packham, G. Stevenson, F.K. (2005) Bodyguards and assassins: Bcl-2 family proteins and apoptosis control in chronic lymphocytic leukaemia. Immunology, 114, 441 449.
31. Pfeiffer, R.M., Goldin, L.R., Chatterjee, N., Daugherty, S., Hemminki, K., Pee, D., X, L.I., Gail, M.H. (2004) Methods for testing familial aggregation of diseases in population-based samples: application to Hodgkin lymphoma in Swedish registry data. Annals of Human Genetics, 68, 498 508.
32. Purdue, M.P., Lan, Q., Kricker, A., Grulich, A.E., Vajdic, C.M., Turner, J., Whitby, D., Chanock, S., Rothman, N. Armstrong, B.K. (2007) Polymorphisms in immune function genes and risk of non-Hodgkin lymphoma: findings from the New South Wales non-Hodgkin Lymphoma Study. Carcinogenesis, 28, 704 712.
33. Raval, A., Tanner, S.M., Byrd, J.C., Angerman, E.B., Perko, J.D., Chen, S.S., Hackanson, B., Grever, M.R., Lucas, D.M., Matkovic, J.J., Lin, T.S., Kipps, T.J., Murray, F., Weisenburger, D., Sanger, W., Lynch, J., Watson, P., Jansen, M., Yoshinaga, Y., Rosenquist, R., de Jong, P.J., Coggill, P., Beck, S., Lynch, H., de la Chapelle, A. Plass, C. (2007) Downregulation of death-associated protein kinase 1 (DAPK1) in chronic lymphocytic leukemia. Cell, 129, 879 890.
34. Rawstron, A.C., Green, M.J., Kuzmicki, A., Kennedy, B., Fenton, J.A., Evans, P.A., O'Connor, S.J., Richards, S.J., Morgan, G.J., Jack, A.S. Hillmen, P. (2002a) Monoclonal B lymphocytes with the characteristics of ''indolent'' chronic lymphocytic leukemia are present in 3.5% of adults with normal blood counts. Blood, 100, 635 639.
35. Rawstron, A.C., Yuille, M.R., Fuller, J., Cullen, M., Kennedy, B., Richards, S.J., Jack, A.S., Matutes, E., Catovsky, D., Hillmen, P. Houlston, R.S. (2002b) Inherited predisposition to CLL is detectable as subclinical monoclonal B-lymphocyte expansion. Blood, 100, 2289 2290.
36. Rawstron, A.C., de Tute, R., O'Connor, S.J.M., Richards, S.J., Jack, A.S. Hillmen, P. (2003) The natural history of ''early CLL''. Blood, 102, 188a.
37. Ries, L.A.G., Melbert, D., Krapcho, M., Mariotto, A., Miller, B.A., Feuer, E.J., Clegg, L., Horner, M.J., Howlader, N., Eisner, M.P., Reichman, M. Edwards, B.K. (2007) Cancer Statistics Review, 1975-2004, National Cancer Institute. In, Vol. 2007, Bethesda, MD http://seer.cancer.gov/csr/1975_2004/.
38. Rothman, N., Skibola, C.F., Wang, S.S., Morgan, G., Lan, Q., Smith, M.T., Spinelli, J.J., Willett, E., De Sanjose, S., Cocco, P., Berndt, S.I., Brennan, P., Brooks-Wilson, A., Wacholder, S., Becker, N., Hartge, P., Zheng, T., Roman, E., Holly, E.A., Boffetta, P., Armstrong, B., Cozen, W., Linet, M., Bosch, F.X., Ennas, M.G., Holford, T.R., Gallagher, R.P., Rollinson, S., Bracci, P.M., Cerhan, J.R., Whitby, D., Moore, P.S., Leaderer, B., Lai, A., Spink, C., Davis, S., Bosch, R., Scarpa, A., Zhang, Y., Severson, R.K., Yeager, M., Chanock, S. Nieters, A. (2006) Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: a report from the InterLymph Consortium. Lancet Oncology, 7, 27 38.
39. Rudd, M.F., Sellick, G.S., Webb, E.L., Catovsky, D. Houlston, R.S. (2006) Variants in the ATM-BRCA2-CHEK2 axis predispose to chronic lymphocytic leukemia. Blood, 108, 638 644.
40. Sakai, A., Marti, G.E., Caporaso, N., Pittaluga, S., Touchman, J.W., Fend, F. Raffeld, M. (2000) Analysis of expressed immunoglobulin heavy chain genes in familial B-CLL. Blood, 95, 1413 1419.
41. Sellick, G.S., Webb, E.L., Allinson, R., Matutes, E., Dyer, M.J., Jonsson, V., Langerak, A.W., Mauro, F.R., Fuller, S., Wiley, J., Lyttelton, M., Callea, V., Yuille, M., Catovsky, D. Houlston, R.S. (2005) A high-density SNP genomewide linkage scan for chronic lymphocytic leukemia-susceptibility loci. American Journal of Human Genetics, 77, 420 429.
42. Sellick, G.S., Catovsky, D. Houlston, R.S. (2006) Familial chronic lymphocytic leukemia. Seminars in Oncology, 33, 195 201.
43. Seymour, J.F., Talpaz, M., Hagemeister, F.B., Cabanillas, F. Kurzrock, R. (1997) Clinical correlates of elevated serum levels of interleukin 6 in patients with untreated Hodgkin's disease. American Journal of Medicine, 102, 21 28.
44. Sgambati, M., Linet, M.S. Devesa, S.S. (2001) Chronic lymphocytic leukemia epidemiological, familial, and genetic aspects. In : Chronic Lymphoid Leukemias Basic and clinical oncology; 26 (ed. by B.D. Cheson pp. 33 62. Marcel Dekker, New York, NY.
45. Slager, S.L., Kay, N.E., Frederiksen, Z.S., Wang, A.H., Liebow, M., Cunningham, J.M., Vachon, C.M., Call, T.G. Cerhan, J.R. (2007) Susceptibility genes and B-chronic lymphocytic leukaemia. British Journal of Haematology, 139, 762 771.
46. Wang, S.S., Cerhan, J.R., Hartge, P., Davis, S., Cozen, W., Severson, R.K., Chatterjee, N., Yeager, M., Chanock, S.J. Rothman, N. (2006) Common genetic variants in proinflammatory and other immunoregulatory genes and risk for non-Hodgkin lymphoma. Cancer Research, 66, 9771 9780.
47. Wang, S.S., Slager, S.L., Brennan, P., Holly, E.A., De Sanjose, S., Bernstein, L., Boffetta, P., Cerhan, J.R., Maynadie, M., Spinelli, J.J., Chiu, B.C., Cocco, P.L., Mensah, F., Zhang, Y., Nieters, A., Dal Maso, L., Bracci, P.M., Costantini, A.S., Vineis, P., Severson, R.K., Roman, E., Cozen, W., Weisenburger, D., Davis, S., Franceschi, S., La Vecchia, C., Foretova, L., Becker, N., Staines, A., Vornanen, M., Zheng, T. Hartge, P. (2007) Family history of hematopoietic malignancies and risk of non-Hodgkin lymphoma (NHL): a pooled analysis of 10 211 cases and 11 905 controls from the International Lymphoma Epidemiology Consortium (InterLymph). Blood, 109, 3479 3488.
48. Yeager, M., Orr, N., Hayes, R.B., Jacobs, K.B., Kraft, P., Wacholder, S., Minichiello, M.J., Fearnhead, P., Yu, K., Chatterjee, N., Wang, Z., Welch, R., Staats, B.J., Calle, E.E., Feigelson, H.S., Thun, M.J., Rodriguez, C., Albanes, D., Virtamo, J., Weinstein, S., Schumacher, F.R., Giovannucci, E., Willett, W.C., Cancel-Tassin, G., Cussenot, O., Valeri, A., Andriole, G.L., Gelmann, E.P., Tucker, M., Gerhard, D.S., Fraumeni, Jr., J.F., Hoover, R., Hunter, D.J., Chanock, S.J. Thomas, G. (2007) Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. Nature Genetics, 39, 645 649.