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Published in: Cancer and Metastasis Reviews 3-4/2009

01-12-2009

Genome-wide association studies of bladder cancer risk: a field synopsis of progress and potential applications

Authors: Xifeng Wu, Michelle A. T. Hildebrandt, David W. Chang

Published in: Cancer and Metastasis Reviews | Issue 3-4/2009

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Abstract

The advent of the genome era after the completion of the Human Genome Project has resulted in intensive efforts to identify all genetic variants that modify human health and disease, including cancer. The development of genome-wide association study (GWAS) approach has facilitated this goal by unbiased examination of the entire human genome for disease association. Here, we review some of the GWAS data, particularly for bladder cancer, and assess their significance in risk prediction and prognosis. A mechanistic understanding of the risk association through functional studies and phenotypic assays is also discussed. The ultimate goal is the development of a comprehensive risk prediction model which integrates genetic, environment, and person risk factors to benefit disease diagnosis, prevention, and treatment.
Literature
1.
go back to reference Hindorff, L. A., Sethupathy, P., Junkins, H. A., Ramos, E. M., Mehta, J. P., Collins, F. S., et al. (2009). Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proceedings of the National Academy of Sciences of the United States of America, 106, 9362–9367.CrossRefPubMed Hindorff, L. A., Sethupathy, P., Junkins, H. A., Ramos, E. M., Mehta, J. P., Collins, F. S., et al. (2009). Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proceedings of the National Academy of Sciences of the United States of America, 106, 9362–9367.CrossRefPubMed
2.
go back to reference Khoury, M. J., Bertram, L., Boffetta, P., Butterworth, A. S., Chanock, S. J., Dolan, S. M., et al. (2009). Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases. American Journal of Epidemiology, 170, 269–279.CrossRefPubMed Khoury, M. J., Bertram, L., Boffetta, P., Butterworth, A. S., Chanock, S. J., Dolan, S. M., et al. (2009). Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases. American Journal of Epidemiology, 170, 269–279.CrossRefPubMed
3.
go back to reference Topol, E. J., Murray, S. S., & Frazer, K. A. (2007). The geonomics gold rush. JAMA, 298, 218–221.CrossRefPubMed Topol, E. J., Murray, S. S., & Frazer, K. A. (2007). The geonomics gold rush. JAMA, 298, 218–221.CrossRefPubMed
5.
go back to reference Easton, D. F., Pooley, K. A., Dunning, A. M., Pharoah, P. D., Thompson, D., Ballinger, D. G., et al. (2007). Genome-wide association study identifies novel breast cancer susceptibility loci. Nature, 447, 1087–1093.CrossRefPubMed Easton, D. F., Pooley, K. A., Dunning, A. M., Pharoah, P. D., Thompson, D., Ballinger, D. G., et al. (2007). Genome-wide association study identifies novel breast cancer susceptibility loci. Nature, 447, 1087–1093.CrossRefPubMed
6.
go back to reference Tomlinson, I., Webb, E., Carvajal-Carmona, L., Broderick, P., Kemp, Z., Spain, S., et al. (2007). A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21. Nature Genetics, 39, 984–988.CrossRefPubMed Tomlinson, I., Webb, E., Carvajal-Carmona, L., Broderick, P., Kemp, Z., Spain, S., et al. (2007). A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21. Nature Genetics, 39, 984–988.CrossRefPubMed
7.
go back to reference Zanke, B. W., Greenwood, C. M., Rangrej, J., Kustra, R., Tenesa, A., Farrington, S. M., et al. (2007). Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24. Nature Genetics, 39, 989–994.CrossRefPubMed Zanke, B. W., Greenwood, C. M., Rangrej, J., Kustra, R., Tenesa, A., Farrington, S. M., et al. (2007). Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24. Nature Genetics, 39, 989–994.CrossRefPubMed
8.
go back to reference Hung, R. J., McKay, J. D., Gaborieau, V., Boffetta, P., Hashibe, M., Zaridze, D., et al. (2008). A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25. Nature, 452, 633–637.CrossRefPubMed Hung, R. J., McKay, J. D., Gaborieau, V., Boffetta, P., Hashibe, M., Zaridze, D., et al. (2008). A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25. Nature, 452, 633–637.CrossRefPubMed
9.
go back to reference Amos, C. I., Wu, X., Broderick, P., Gorlov, I. P., Gu, J., Eisen, T., et al. (2008). Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. Nature Genetics, 40, 616–622.CrossRefPubMed Amos, C. I., Wu, X., Broderick, P., Gorlov, I. P., Gu, J., Eisen, T., et al. (2008). Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. Nature Genetics, 40, 616–622.CrossRefPubMed
10.
go back to reference Amundadottir, L. T., Sulem, P., Gudmundsson, J., Helgason, A., Baker, A., Agnarsson, B. A., et al. (2006). A common variant associated with prostate cancer in European and African populations. Nature Genetics, 38, 652–658.CrossRefPubMed Amundadottir, L. T., Sulem, P., Gudmundsson, J., Helgason, A., Baker, A., Agnarsson, B. A., et al. (2006). A common variant associated with prostate cancer in European and African populations. Nature Genetics, 38, 652–658.CrossRefPubMed
11.
go back to reference Yeager, M., Chatterjee, N., Ciampa, J., Jacobs, K. B., Gonzalez-Bosquet, J., Hayes, R. B., et al. (2009). Identification of a new prostate cancer susceptibility locus on chromosome 8q24. Nature Genetics, 41, 1055–1057.CrossRefPubMed Yeager, M., Chatterjee, N., Ciampa, J., Jacobs, K. B., Gonzalez-Bosquet, J., Hayes, R. B., et al. (2009). Identification of a new prostate cancer susceptibility locus on chromosome 8q24. Nature Genetics, 41, 1055–1057.CrossRefPubMed
12.
go back to reference Wu, X., Ye, Y., Kiemeney, L. A., Sulem, P., Rafnar, T., Matullo, G., et al. (2009). Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer. Nature Genetics, 41, 991–995.CrossRefPubMed Wu, X., Ye, Y., Kiemeney, L. A., Sulem, P., Rafnar, T., Matullo, G., et al. (2009). Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer. Nature Genetics, 41, 991–995.CrossRefPubMed
13.
go back to reference Song, H., Ramus, S. J., Tyrer, J., Bolton, K. L., Gentry-Maharaj, A., Wozniak, E., et al. (2009). A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2. Nature Genetics, 41, 996–1000.CrossRefPubMed Song, H., Ramus, S. J., Tyrer, J., Bolton, K. L., Gentry-Maharaj, A., Wozniak, E., et al. (2009). A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2. Nature Genetics, 41, 996–1000.CrossRefPubMed
14.
go back to reference Amundadottir, L., Kraft, P., Stolzenberg-Solomon, R. Z., Fuchs, C. S., Petersen, G. M., Arslan, A. A., et al. (2009). Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer. Nature Genetics, 41, 986–990.CrossRefPubMed Amundadottir, L., Kraft, P., Stolzenberg-Solomon, R. Z., Fuchs, C. S., Petersen, G. M., Arslan, A. A., et al. (2009). Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer. Nature Genetics, 41, 986–990.CrossRefPubMed
15.
go back to reference Kiemeney, L. A., Thorlacius, S., Sulem, P., Geller, F., Aben, K. K., Stacey, S. N., et al. (2008). Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. Nature Genetics, 40, 1307–1312.CrossRefPubMed Kiemeney, L. A., Thorlacius, S., Sulem, P., Geller, F., Aben, K. K., Stacey, S. N., et al. (2008). Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. Nature Genetics, 40, 1307–1312.CrossRefPubMed
16.
go back to reference International Human Genome Sequencing Consortium, Lander, E. S., Linton, L. M., Birren, B., Nusbaum, C., Zody, M. C., et al. (2001). Initial sequencing and analysis of the human genome. Nature, 409, 860–921.CrossRefPubMed International Human Genome Sequencing Consortium, Lander, E. S., Linton, L. M., Birren, B., Nusbaum, C., Zody, M. C., et al. (2001). Initial sequencing and analysis of the human genome. Nature, 409, 860–921.CrossRefPubMed
17.
go back to reference Venter, J. C., Adams, M. D., Myers, E. W., Li, P. W., Mural, R. J., Sutton, G. G., et al. (2001). The sequence of the human genome. Science, 291, 1304–1351.CrossRefPubMed Venter, J. C., Adams, M. D., Myers, E. W., Li, P. W., Mural, R. J., Sutton, G. G., et al. (2001). The sequence of the human genome. Science, 291, 1304–1351.CrossRefPubMed
18.
go back to reference Malkin, D., Li, F. P., Strong, L. C., Fraumeni, J. F., Jr., Nelson, C. E., Kim, D. H., et al. (1990). Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. Science, 250, 1233–1238.CrossRefPubMed Malkin, D., Li, F. P., Strong, L. C., Fraumeni, J. F., Jr., Nelson, C. E., Kim, D. H., et al. (1990). Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. Science, 250, 1233–1238.CrossRefPubMed
19.
go back to reference Dalla-Favera, R., Bregni, M., Erikson, J., Patterson, D., Gallo, R. C., & Croce, C. M. (1982). Human c-myc onc gene is located on the region of chromosome 8 that is translocated in Burkitt lymphoma cells. Proceedings of the National Academy of Sciences of the United States of America, 79, 7824–7827.CrossRefPubMed Dalla-Favera, R., Bregni, M., Erikson, J., Patterson, D., Gallo, R. C., & Croce, C. M. (1982). Human c-myc onc gene is located on the region of chromosome 8 that is translocated in Burkitt lymphoma cells. Proceedings of the National Academy of Sciences of the United States of America, 79, 7824–7827.CrossRefPubMed
20.
go back to reference Suzuki, H., Watkins, D. N., Jair, K. W., Schuebel, K. E., Markowitz, S. D., Chen, W. D., et al. (2004). Epigenetic inactivation of SFRP genes allows constitutive WNT signaling in colorectal cancer. Nature Genetics, 36, 417–422.CrossRefPubMed Suzuki, H., Watkins, D. N., Jair, K. W., Schuebel, K. E., Markowitz, S. D., Chen, W. D., et al. (2004). Epigenetic inactivation of SFRP genes allows constitutive WNT signaling in colorectal cancer. Nature Genetics, 36, 417–422.CrossRefPubMed
21.
go back to reference The International HapMap Consortium. (2005). A haplotype map of the human genome. Nature, 437, 1299–1320.CrossRef The International HapMap Consortium. (2005). A haplotype map of the human genome. Nature, 437, 1299–1320.CrossRef
22.
go back to reference The International HapMap Consortium. (2007). A second generation human haplotype map of over 3.1 million SNPs. Nature, 449, 851–861.CrossRef The International HapMap Consortium. (2007). A second generation human haplotype map of over 3.1 million SNPs. Nature, 449, 851–861.CrossRef
23.
go back to reference Reich, D. E., & Lander, E. S. (2001). On the allelic spectrum of human disease. Trends in Genetics, 17, 502–510.CrossRefPubMed Reich, D. E., & Lander, E. S. (2001). On the allelic spectrum of human disease. Trends in Genetics, 17, 502–510.CrossRefPubMed
24.
go back to reference Kiemeney, L. A., Grotenhuis, A. J., Vermeulen, S. H., & Wu, X. (2009). Genome-wide association studies in bladder cancer: First results and potential relevance. Current Opinion in Urology, 19, 540–546.CrossRefPubMed Kiemeney, L. A., Grotenhuis, A. J., Vermeulen, S. H., & Wu, X. (2009). Genome-wide association studies in bladder cancer: First results and potential relevance. Current Opinion in Urology, 19, 540–546.CrossRefPubMed
25.
go back to reference Easton, D. F., & Eeles, R. A. (2008). Genome-wide association studies in cancer. Human Molecular Genetics, 17, R109–R115.CrossRefPubMed Easton, D. F., & Eeles, R. A. (2008). Genome-wide association studies in cancer. Human Molecular Genetics, 17, R109–R115.CrossRefPubMed
26.
go back to reference Panagopoulos, I., Möller, E., Collin, A., & Mertens, F. (2008). The POU5F1P1 pseudogene encodes a putative protein similar to POU5F1 isoform 1. Oncology Reports, 20, 1029–1033.PubMed Panagopoulos, I., Möller, E., Collin, A., & Mertens, F. (2008). The POU5F1P1 pseudogene encodes a putative protein similar to POU5F1 isoform 1. Oncology Reports, 20, 1029–1033.PubMed
27.
go back to reference Wang, M., Wang, M., Zhang, W., Yuan, L., Fu, G., Wei, Q., et al. (2009). Common genetic variants on 8q24 contribute to susceptibility to bladder cancer in a Chinese population. Carcinogenesis, 30, 991–996.CrossRefPubMed Wang, M., Wang, M., Zhang, W., Yuan, L., Fu, G., Wei, Q., et al. (2009). Common genetic variants on 8q24 contribute to susceptibility to bladder cancer in a Chinese population. Carcinogenesis, 30, 991–996.CrossRefPubMed
28.
go back to reference Stern, M. C., Van Den Berg, D., Yuan, J. M., Conti, D. V., Gago-Dominguez, M., Pike, M. C., et al. (2009). Sequence variant on 3q28 and urinary bladder cancer risk: Findings from the Los Angeles–Shanghai bladder case–control study. Cancer Epidemiology, Biomarkers and Prevention, 18, 3057–3061.CrossRefPubMed Stern, M. C., Van Den Berg, D., Yuan, J. M., Conti, D. V., Gago-Dominguez, M., Pike, M. C., et al. (2009). Sequence variant on 3q28 and urinary bladder cancer risk: Findings from the Los Angeles–Shanghai bladder case–control study. Cancer Epidemiology, Biomarkers and Prevention, 18, 3057–3061.CrossRefPubMed
29.
go back to reference Park, B. J., Lee, S. J., Kim, J. I., Lee, S. J., Lee, C. H., Chang, S. G., et al. (2000). Frequent alteration of p63 expression in human primary bladder carcinomas. Cancer Research, 60, 3370–3374.PubMed Park, B. J., Lee, S. J., Kim, J. I., Lee, S. J., Lee, C. H., Chang, S. G., et al. (2000). Frequent alteration of p63 expression in human primary bladder carcinomas. Cancer Research, 60, 3370–3374.PubMed
30.
go back to reference Urist, M. J., Di Como, C. J., Lu, M. L., Charytonowicz, E., Verbel, D., Crum, C. P., et al. (2002). Loss of p63 expression is associated with tumor progression in bladder cancer. American Journal of Pathology, 161, 1199–1206.PubMed Urist, M. J., Di Como, C. J., Lu, M. L., Charytonowicz, E., Verbel, D., Crum, C. P., et al. (2002). Loss of p63 expression is associated with tumor progression in bladder cancer. American Journal of Pathology, 161, 1199–1206.PubMed
31.
go back to reference Koga, F., Kawakami, S., Fuji, Y., Saito, K., Ohtsuka, Y., Iwai, A., et al. (2003). Impaired p63 expression associates with poor prognosis and uroplakin III expression in invasive urothelial carcinoma of the bladder. Clinical Cancer Research, 9, 5501–5507.PubMed Koga, F., Kawakami, S., Fuji, Y., Saito, K., Ohtsuka, Y., Iwai, A., et al. (2003). Impaired p63 expression associates with poor prognosis and uroplakin III expression in invasive urothelial carcinoma of the bladder. Clinical Cancer Research, 9, 5501–5507.PubMed
32.
go back to reference Reiter, R. E., Gu, Z., Watabe, T., Thomas, G., Szigeti, K., Davis, E., et al. (1998). Prostate stem cell antigen: A cell surface marker overexpressed in prostate cancer. Proceedings of the National Academy of Sciences of the United States of America, 95, 1735–1740.CrossRefPubMed Reiter, R. E., Gu, Z., Watabe, T., Thomas, G., Szigeti, K., Davis, E., et al. (1998). Prostate stem cell antigen: A cell surface marker overexpressed in prostate cancer. Proceedings of the National Academy of Sciences of the United States of America, 95, 1735–1740.CrossRefPubMed
33.
go back to reference Amara, N., Palapattu, G. S., Schrage, M., Gu, Z., Thomas, G. V., Dorey, F., et al. (2001). Prostate stem cell antigen is overexpressed in human transitional cell carcinoma. Cancer Research, 61, 4660–4665.PubMed Amara, N., Palapattu, G. S., Schrage, M., Gu, Z., Thomas, G. V., Dorey, F., et al. (2001). Prostate stem cell antigen is overexpressed in human transitional cell carcinoma. Cancer Research, 61, 4660–4665.PubMed
34.
go back to reference Elsamman, E. M., Fukumori, T., Tanimoto, S., Nakanishi, R., Takahashi, M., Toida, K., et al. (2006). The expression of prostate stem cell antigen in human clear cell renal cell carcinoma: A quantitative reverse transcriptase-polymerase chain reaction analysis. BJU International, 98, 668–673.CrossRefPubMed Elsamman, E. M., Fukumori, T., Tanimoto, S., Nakanishi, R., Takahashi, M., Toida, K., et al. (2006). The expression of prostate stem cell antigen in human clear cell renal cell carcinoma: A quantitative reverse transcriptase-polymerase chain reaction analysis. BJU International, 98, 668–673.CrossRefPubMed
35.
go back to reference Argani, P., Rosty, C., Reiter, R. E., Wilentz, R. E., Murugesan, S. R., Leach, S. D., et al. (2001). Discovery of new markers of cancer through serial analysis of gene expression: Prostate stem cell antigen is overexpressed in pancreatic adenocarcinoma. Cancer Research, 61, 4320–4324.PubMed Argani, P., Rosty, C., Reiter, R. E., Wilentz, R. E., Murugesan, S. R., Leach, S. D., et al. (2001). Discovery of new markers of cancer through serial analysis of gene expression: Prostate stem cell antigen is overexpressed in pancreatic adenocarcinoma. Cancer Research, 61, 4320–4324.PubMed
36.
go back to reference Gu, Z., Thomas, G., Yamashiro, J., Shintaku, I. P., Dorey, F., Raitano, A., et al. (2000). Prostate stem cell antigen (PSCA) expression increases with high Gleason score, advanced stage and bone metastasis in prostate cancer. Oncogene, 19, 1288–1296.CrossRefPubMed Gu, Z., Thomas, G., Yamashiro, J., Shintaku, I. P., Dorey, F., Raitano, A., et al. (2000). Prostate stem cell antigen (PSCA) expression increases with high Gleason score, advanced stage and bone metastasis in prostate cancer. Oncogene, 19, 1288–1296.CrossRefPubMed
37.
go back to reference Cheng, L., Reiter, R. E., Jin, Y., Sharon, H., Wieder, J., Lane, T. F., et al. (2003). Immunocytochemical analysis of prostate stem cell antigen as adjunct marker for detection of urothelial transitional cell carcinoma in voided urine specimens. Journal of Urology, 169, 2094–2100.CrossRefPubMed Cheng, L., Reiter, R. E., Jin, Y., Sharon, H., Wieder, J., Lane, T. F., et al. (2003). Immunocytochemical analysis of prostate stem cell antigen as adjunct marker for detection of urothelial transitional cell carcinoma in voided urine specimens. Journal of Urology, 169, 2094–2100.CrossRefPubMed
38.
go back to reference Study Group of Millennium Genome Project for Cancer, Sakamoto, H., Yoshimura, K., Saeki, N., Katai, H., Shimoda, T., et al. (2008). Genetic variation in PSCA is associated with susceptibility to diffuse-type gastric cancer. Nature Genetics, 40, 730–740.CrossRefPubMed Study Group of Millennium Genome Project for Cancer, Sakamoto, H., Yoshimura, K., Saeki, N., Katai, H., Shimoda, T., et al. (2008). Genetic variation in PSCA is associated with susceptibility to diffuse-type gastric cancer. Nature Genetics, 40, 730–740.CrossRefPubMed
39.
go back to reference Moore, M. L., Teitell, M. A., Kim, Y., Watabe, T., Reiter, R. E., Witte, O. N., et al. (2008). Deletion of PSCA increases metastasis of TRAMP-induced prostate tumors without altering primary tumor formation. Prostate, 68, 139–151.CrossRefPubMed Moore, M. L., Teitell, M. A., Kim, Y., Watabe, T., Reiter, R. E., Witte, O. N., et al. (2008). Deletion of PSCA increases metastasis of TRAMP-induced prostate tumors without altering primary tumor formation. Prostate, 68, 139–151.CrossRefPubMed
40.
go back to reference Rafnar, T., Sulem, P., Stacey, S. N., Geller, F., Gudmundsson, J., Sigurdsson, A., et al. (2009). Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. Nature Genetics, 41, 221–227.CrossRefPubMed Rafnar, T., Sulem, P., Stacey, S. N., Geller, F., Gudmundsson, J., Sigurdsson, A., et al. (2009). Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. Nature Genetics, 41, 221–227.CrossRefPubMed
41.
go back to reference Hunter, D. J., Kraft, P., Jacobs, K. B., Cox, D. G., Yeager, M., Hankinson, S. E., et al. (2007). A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nature Genetics, 39, 870–874.CrossRefPubMed Hunter, D. J., Kraft, P., Jacobs, K. B., Cox, D. G., Yeager, M., Hankinson, S. E., et al. (2007). A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nature Genetics, 39, 870–874.CrossRefPubMed
42.
go back to reference Gold, B., Kirchhoff, T., Stefanov, S., Lautenberger, J., Viale, A., Garber, J., et al. (2008). Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33. Proceedings of the National Academy of Sciences of the United States of America, 105, 4340–4345.CrossRefPubMed Gold, B., Kirchhoff, T., Stefanov, S., Lautenberger, J., Viale, A., Garber, J., et al. (2008). Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33. Proceedings of the National Academy of Sciences of the United States of America, 105, 4340–4345.CrossRefPubMed
43.
go back to reference Gail, M. H. (2008). Discriminatory accuracy from single-nucleotide polymorphisms in models to predict breast cancer risk. Journal of the National Cancer Institute, 100, 1037–1041.CrossRefPubMed Gail, M. H. (2008). Discriminatory accuracy from single-nucleotide polymorphisms in models to predict breast cancer risk. Journal of the National Cancer Institute, 100, 1037–1041.CrossRefPubMed
44.
go back to reference Gail, M. H. (2009). Value of adding single-nucleotide polymorphism genotypes to a breast cancer risk model. Journal of the National Cancer Institute, 101, 959–963.CrossRefPubMed Gail, M. H. (2009). Value of adding single-nucleotide polymorphism genotypes to a breast cancer risk model. Journal of the National Cancer Institute, 101, 959–963.CrossRefPubMed
45.
go back to reference Leibovici, D., Grossman, H. B., Dinney, C. P., Millikan, R. E., Lerner, S., Wang, Y., et al. (2005). Polymorphisms in inflammation genes and bladder cancer: From initiation to recurrence, progression, and survival. Journal of Clinical Oncology, 23, 5746–5756.CrossRefPubMed Leibovici, D., Grossman, H. B., Dinney, C. P., Millikan, R. E., Lerner, S., Wang, Y., et al. (2005). Polymorphisms in inflammation genes and bladder cancer: From initiation to recurrence, progression, and survival. Journal of Clinical Oncology, 23, 5746–5756.CrossRefPubMed
46.
go back to reference Hsu, T. C., Johnston, D. A., Cherry, L. M., Ramkissoon, D., Schantz, S. P., Jessup, J. M., et al. (1989). Sensitivity to genotoxic effects of bleomycin in humans: Possible relationship to environmental carcinogenesis. International Journal of Cancer, 43, 403–409.CrossRef Hsu, T. C., Johnston, D. A., Cherry, L. M., Ramkissoon, D., Schantz, S. P., Jessup, J. M., et al. (1989). Sensitivity to genotoxic effects of bleomycin in humans: Possible relationship to environmental carcinogenesis. International Journal of Cancer, 43, 403–409.CrossRef
47.
go back to reference Ziegler, A., König, I. R., & Thompson, J. R. (2008). Biostatistical aspects of genome-wide association studies. Biometrical Journal, 50, 8–28.CrossRefPubMed Ziegler, A., König, I. R., & Thompson, J. R. (2008). Biostatistical aspects of genome-wide association studies. Biometrical Journal, 50, 8–28.CrossRefPubMed
48.
go back to reference Wu, X., Lin, J., Grossman, H. B., Huang, M., Gu, J., Etzel, C. J., et al. (2007). Projecting individualized probabilities of developing bladder cancer in white individuals. Journal of Clinical Oncology, 25, 4974–4981.CrossRefPubMed Wu, X., Lin, J., Grossman, H. B., Huang, M., Gu, J., Etzel, C. J., et al. (2007). Projecting individualized probabilities of developing bladder cancer in white individuals. Journal of Clinical Oncology, 25, 4974–4981.CrossRefPubMed
Metadata
Title
Genome-wide association studies of bladder cancer risk: a field synopsis of progress and potential applications
Authors
Xifeng Wu
Michelle A. T. Hildebrandt
David W. Chang
Publication date
01-12-2009
Publisher
Springer US
Published in
Cancer and Metastasis Reviews / Issue 3-4/2009
Print ISSN: 0167-7659
Electronic ISSN: 1573-7233
DOI
https://doi.org/10.1007/s10555-009-9190-y

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