All Genetic Epidemiology Branch investigations evaluate the contributions of host susceptibility and environmental exposure in the development of cancer. A broad range of study designs are utilized, varying from family studies for linkage analysis, to biochemical epidemiology studies, to more classical case-control and cohort studies. Most investigators included a laboratory component. To facilitate efforts in gene mapping, a formal agreement with the Laboratory of Viral Carcinogenesis has been established and is functioning well. This year, genetic heterogeneity was demonstrated in the melanoma-prone families, with some families linked to 1p36, some to 9p21-22, and some to both. A new familial clustering of tumors, Ewings sarcoma family of tumors, melanoma, brain, and stomach cancers was described. The CYP2D6 phenotype and genotype did not appear to be associated with lung cancer risk in a case-control study of lung cancer. Second lung cancers were linked to continued cigarette smoking, and to a lesser extent, chest irradiation. The risk of myocardial infarction after Hodgkin's disease is 3-fold increased overall and is related to mediastinal radiation. The risk is over 40-fold in- creased in those irradiated before age 20. New investigations of the familiarity of dysplastic nevi and of Beckwith-Wiedemann syndrome were initiated.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Intramural Research (Z01)
Project #
1Z01CP004410-94
Application #
3752597
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
94
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Division of Cancer Epidemiology and Genetics
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Goldin, Lynn R; McMaster, Mary L; Caporaso, Neil E (2013) Precursors to lymphoproliferative malignancies. Cancer Epidemiol Biomarkers Prev 22:533-9
Han, Summer S; Yeager, Meredith; Moore, Lee E et al. (2012) The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma. Hum Mol Genet 21:1190-200
Brau-Javier, Cristina N; Gonzales-Chavez, Jose; Toro, Jorge R (2012) Chronic cutaneous pustulosis due to a 175-kb deletion on chromosome 2q13: excellent response to anakinra. Arch Dermatol 148:301-4
Kristinsson, Sigurdur Y; Goldin, Lynn R; Turesson, Ingemar et al. (2012) Familial aggregation of lymphoplasmacytic lymphoma/Waldenström macroglobulinemia with solid tumors and myeloid malignancies. Acta Haematol 127:173-7
Goldin, Lynn R; Kristinsson, Sigurdur Y; Liang, Xueying Sharon et al. (2012) Familial aggregation of acute myeloid leukemia and myelodysplastic syndromes. J Clin Oncol 30:179-83
Lindqvist, Ebba K; Goldin, Lynn R; Landgren, Ola et al. (2011) Personal and family history of immune-related conditions increase the risk of plasma cell disorders: a population-based study. Blood 118:6284-91
Goldin, Lynn R; Lanasa, Mark C; Slager, Susan L et al. (2010) Common occurrence of monoclonal B-cell lymphocytosis among members of high-risk CLL families. Br J Haematol 151:152-8
Kristinsson, Sigurdur Y; Björkholm, Magnus; Goldin, Lynn R et al. (2009) Patterns of hematologic malignancies and solid tumors among 37,838 first-degree relatives of 13,896 patients with multiple myeloma in Sweden. Int J Cancer 125:2147-50
Bradford, Porcia T; Goldstein, Alisa M; McMaster, Mary L et al. (2009) Acral lentiginous melanoma: incidence and survival patterns in the United States, 1986-2005. Arch Dermatol 145:427-34
Kristinsson, Sigurdur Y; Koshiol, Jill; Goldin, Lynn R et al. (2009) Genetics- and immune-related factors in the pathogenesis of lymphoplasmacytic lymphoma/ Waldenström's macroglobulinemia. Clin Lymphoma Myeloma 9:23-6

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