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Published in: Cancer and Metastasis Reviews 2/2010

01-06-2010 | NON-THEMATIC REVIEW

Hereditary ovarian cancers: from BRCA mutations to clinical management. A modern appraisal

Authors: Andrea Tinelli, Antonio Malvasi, Giuseppe Leo, Daniele Vergara, Maurizio Pisanò, Mariangela Ciccarese, Vincenzo Emanuele Chiuri, Vito Lorusso

Published in: Cancer and Metastasis Reviews | Issue 2/2010

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Abstract

In the past few years, ovarian cancer research has focused increasingly on disease prevention; but an increasing number of women refer to gynecology and clinical genetics clinics with a family history of ovarian cancer and inherited familial mutations. The interest on the issue has increased also due to the identification of BReast CAncer1 (BRCA1) and BRCA2 genes mutations. The importance of recognizing the characteristics of hereditary ovarian cancer (HOC) and manage women at risk appropriately will provide more accurate care of the high-risk population. Women at risk can be identified by pedigree analysis and may receive counseling from interdisciplinary cancer genetics clinics, while those at high risk need to receive genetic testing. Risk calculation programs define risks and assist in decision-making in clinical options and genetic testing; they provide information on the risks of the disease, mutation status, and the use of genetic testing in the management of high-risk families. Furthermore, while a large number of surrogate preliminary markers have been identified, there are still limited studies on ovarian cancer genomics. Different options for risk management of HOC are available: surveillance, chemoprevention and prophylactic surgery. Surveillance in HOC high-risk patients is still not accurate. Chemoprevention is currently a controversial topic, because a number of major issues still need to be addressed in developing and testing agents for ovarian cancer chemoprevention. Prophylactic surgery has been shown to effectively decrease cancer risk, and it has the possibility to substantially reduce ovarian cancer mortality.
Literature
1.
go back to reference Tinelli, A., Vergara, D., Martignago, R., Leo, G., Pisanò, M., & Malvasi, A. (2009). An outlook on ovarian cancer and borderline ovarian tumors: focus on genomic and proteomic findings. Current Genomics, 4(10), 240–249.CrossRef Tinelli, A., Vergara, D., Martignago, R., Leo, G., Pisanò, M., & Malvasi, A. (2009). An outlook on ovarian cancer and borderline ovarian tumors: focus on genomic and proteomic findings. Current Genomics, 4(10), 240–249.CrossRef
2.
go back to reference Sankaranarayanan, R., & Ferlay, J. (2006). Worldwide burden of gynaecological cancer: the size of the problem. Best Practice & Research Clinical Obstetrics Gynaecology, 20, 207–225.CrossRef Sankaranarayanan, R., & Ferlay, J. (2006). Worldwide burden of gynaecological cancer: the size of the problem. Best Practice & Research Clinical Obstetrics Gynaecology, 20, 207–225.CrossRef
3.
go back to reference Lynch, H. T., Snyder, C. L., Lynch, J. F., Riley, B. D., & Rubinstein, W. S. (2003). Hereditary breast-ovarian cancer at the bedside: role of the medical oncologist. Journal of Clinical Oncology, 21, 740–753.CrossRefPubMed Lynch, H. T., Snyder, C. L., Lynch, J. F., Riley, B. D., & Rubinstein, W. S. (2003). Hereditary breast-ovarian cancer at the bedside: role of the medical oncologist. Journal of Clinical Oncology, 21, 740–753.CrossRefPubMed
4.
go back to reference Lynch, H. T., Krush, A. J., Lemon, H. M., et al. (1972). Tumor variation in families with breast cancer. Jama, 222, 1631–1635.CrossRefPubMed Lynch, H. T., Krush, A. J., Lemon, H. M., et al. (1972). Tumor variation in families with breast cancer. Jama, 222, 1631–1635.CrossRefPubMed
5.
go back to reference Nielsen, F. C., Kruse, T. A., & Gerdes, A. M. (2008). BRCA1 and BRCA2 mutations in Danish families with hereditary breast and/or ovarian cancer. Acta Oncologica, 47(4), 772–777.CrossRefPubMed Nielsen, F. C., Kruse, T. A., & Gerdes, A. M. (2008). BRCA1 and BRCA2 mutations in Danish families with hereditary breast and/or ovarian cancer. Acta Oncologica, 47(4), 772–777.CrossRefPubMed
6.
go back to reference Sinilnikova, O. M., Mazoyer, S., Bonnardel, C., Lynch, H. T., Narod, S. A., & Lenoir, G. M. (2006). BRCA1 and BRCA2 mutations in breast and ovarian cancer syndrome: reflection on the Creighton University historical series of high-risk families. Familial Cancer, 5, 15–20.CrossRefPubMed Sinilnikova, O. M., Mazoyer, S., Bonnardel, C., Lynch, H. T., Narod, S. A., & Lenoir, G. M. (2006). BRCA1 and BRCA2 mutations in breast and ovarian cancer syndrome: reflection on the Creighton University historical series of high-risk families. Familial Cancer, 5, 15–20.CrossRefPubMed
7.
go back to reference Brunet, J., & Pèrez-Segura, P. (2004). Cancer screening and genetic counselling. Reviews in oncology, 6(3), 176–183. Brunet, J., & Pèrez-Segura, P. (2004). Cancer screening and genetic counselling. Reviews in oncology, 6(3), 176–183.
8.
go back to reference Ries LAG, Harkins D, Krapcho M, Mariotto A, Miller BA, Feuer ES, et al. (eds). SEER Cancer Statistics Review, 1975 – 2004, National Cancer Institute, Bethesda, http://seer.cancer.gov/csr/1975_2004/, based on November 2006 SEER data submission, posted to the SEER website 2007 Ries LAG, Harkins D, Krapcho M, Mariotto A, Miller BA, Feuer ES, et al. (eds). SEER Cancer Statistics Review, 1975 – 2004, National Cancer Institute, Bethesda, http://​seer.​cancer.​gov/​csr/​1975_​2004/​, based on November 2006 SEER data submission, posted to the SEER website 2007
9.
go back to reference Kurian, A. W., Balise, R. R., McGuire, V., & Whittemore, A. S. (2005). Histologic types of epithelial ovarian cancer: have they different risk factors? Gynecologic Oncology, 96, 520–530.CrossRefPubMed Kurian, A. W., Balise, R. R., McGuire, V., & Whittemore, A. S. (2005). Histologic types of epithelial ovarian cancer: have they different risk factors? Gynecologic Oncology, 96, 520–530.CrossRefPubMed
10.
go back to reference Chiaffarino, F., Parazzini, F., Bosetti, C., Franceschi, S., Talamini, R., Canzonieri, V., et al. (2007). Risk factors for ovarian cancer histotypes. European Journal of Cancer, 43, 1208–1213.CrossRefPubMed Chiaffarino, F., Parazzini, F., Bosetti, C., Franceschi, S., Talamini, R., Canzonieri, V., et al. (2007). Risk factors for ovarian cancer histotypes. European Journal of Cancer, 43, 1208–1213.CrossRefPubMed
11.
go back to reference Bray, F., Loos, A. H., Tognazzo, S., & La Vecchia, C. (2005). Ovarian cancer in Europe: cross-sectional trends in incidence and mortality in 28 countries, 1953–2000. International Journal of Cancer, 113, 977–990.CrossRef Bray, F., Loos, A. H., Tognazzo, S., & La Vecchia, C. (2005). Ovarian cancer in Europe: cross-sectional trends in incidence and mortality in 28 countries, 1953–2000. International Journal of Cancer, 113, 977–990.CrossRef
12.
go back to reference Negri, E., Pelucchi, C., Franceschi, S., Montella, M., Conti, E., Dal Maso, L., et al. (2003). Family history of cancer and risk of ovarian cancer. European Journal of Cancer, 39, 505–510.CrossRefPubMed Negri, E., Pelucchi, C., Franceschi, S., Montella, M., Conti, E., Dal Maso, L., et al. (2003). Family history of cancer and risk of ovarian cancer. European Journal of Cancer, 39, 505–510.CrossRefPubMed
13.
go back to reference La Vecchia, C. (2001). Epidemiology of ovarian cancer: a summary review. European Journal of Cancer Prevention, 10, 125–129.CrossRefPubMed La Vecchia, C. (2001). Epidemiology of ovarian cancer: a summary review. European Journal of Cancer Prevention, 10, 125–129.CrossRefPubMed
14.
go back to reference Simon, M. S., & Petrucelli, N. (2009). Hereditary breast and ovarian cancer syndrome: the impact of race on uptake of genetic counseling and testing. Methods in Molecular Biology, 471, 487–500.CrossRefPubMed Simon, M. S., & Petrucelli, N. (2009). Hereditary breast and ovarian cancer syndrome: the impact of race on uptake of genetic counseling and testing. Methods in Molecular Biology, 471, 487–500.CrossRefPubMed
15.
go back to reference Chen, Y., Farmer, A. A., Chen, C. F., Jones, D. C., Chen, P. L., & Lee, W. H. (1996). BRCA1 is a 220-kDa nuclear phosphoprotein that is expressed and phosphorylated in a cell cycle-dependent manner. Cancer Research, 56, 3168–3172.PubMed Chen, Y., Farmer, A. A., Chen, C. F., Jones, D. C., Chen, P. L., & Lee, W. H. (1996). BRCA1 is a 220-kDa nuclear phosphoprotein that is expressed and phosphorylated in a cell cycle-dependent manner. Cancer Research, 56, 3168–3172.PubMed
16.
go back to reference Ruffner, H., & Verma, I. M. (1997). BRCA1 is a cell cycle-regulated nuclear phosphoprotein. Proceedings of the National Academy of Sciences of the United States of America, 94, 7138–7143.CrossRefPubMed Ruffner, H., & Verma, I. M. (1997). BRCA1 is a cell cycle-regulated nuclear phosphoprotein. Proceedings of the National Academy of Sciences of the United States of America, 94, 7138–7143.CrossRefPubMed
17.
go back to reference Deng, C. X. (2006). BRCA1: cell cycle checkpoint, genetic instability, DNA damage response and cancer evolution. Nucleic Acids Research, 34(5), 1416–1426.CrossRefPubMed Deng, C. X. (2006). BRCA1: cell cycle checkpoint, genetic instability, DNA damage response and cancer evolution. Nucleic Acids Research, 34(5), 1416–1426.CrossRefPubMed
18.
go back to reference Yu, X. C., CC, He M., Mer, G., & Chen, J. (2003). The BRCT domain is a phospho-protein binding domain. Science, 302, 639–642.CrossRefPubMed Yu, X. C., CC, He M., Mer, G., & Chen, J. (2003). The BRCT domain is a phospho-protein binding domain. Science, 302, 639–642.CrossRefPubMed
19.
go back to reference Manke, I. A., Lowery, D. M., Nguyen, A., & Yaffe, M. B. (2003). BRCT repeats as phosphopeptide-binding modules involved in protein targeting. Science, 302, 636–639.CrossRefPubMed Manke, I. A., Lowery, D. M., Nguyen, A., & Yaffe, M. B. (2003). BRCT repeats as phosphopeptide-binding modules involved in protein targeting. Science, 302, 636–639.CrossRefPubMed
20.
go back to reference Arai, M., Utsunomiya, J., & Miki, Y. (2004). Familial breast and ovarian cancers. International Journal of Clinical Oncology, 9, 270–282.CrossRefPubMed Arai, M., Utsunomiya, J., & Miki, Y. (2004). Familial breast and ovarian cancers. International Journal of Clinical Oncology, 9, 270–282.CrossRefPubMed
21.
go back to reference Ouchi, T., Monteiro, A. N., August, A., Aaronson, S. A., & Hanafusa, H. (1998). BRCA1 regulates p53-dependent gene expression. Proceedings of the National Academy of Sciences of the United States of America, 95(5), 2302–2306.CrossRefPubMed Ouchi, T., Monteiro, A. N., August, A., Aaronson, S. A., & Hanafusa, H. (1998). BRCA1 regulates p53-dependent gene expression. Proceedings of the National Academy of Sciences of the United States of America, 95(5), 2302–2306.CrossRefPubMed
22.
go back to reference Fan, S., Yong, X., Wang, C., Yuan, R. Q., Meng, Q., Wang, J. A., et al. (2001). Role of direct interaction in BRCA1 inhibition of estrogen receptor activity. Oncogene, 20(1), 77–87.CrossRefPubMed Fan, S., Yong, X., Wang, C., Yuan, R. Q., Meng, Q., Wang, J. A., et al. (2001). Role of direct interaction in BRCA1 inhibition of estrogen receptor activity. Oncogene, 20(1), 77–87.CrossRefPubMed
23.
go back to reference Zheng, L., Annab, L. A., Afshari, C. A., Lee, W. H., & Boyer, T. G. (2001). BRCA1 mediates ligand-independent transcriptional repression of the estrogen receptor. Proceedings of the National Academy of Sciences of the United States of America, 98(17), 9587–9592.CrossRefPubMed Zheng, L., Annab, L. A., Afshari, C. A., Lee, W. H., & Boyer, T. G. (2001). BRCA1 mediates ligand-independent transcriptional repression of the estrogen receptor. Proceedings of the National Academy of Sciences of the United States of America, 98(17), 9587–9592.CrossRefPubMed
24.
go back to reference Rajan, J. V., Wang, M., Marquis, S. T., & Chodosh, L. A. (1996). Brca2 is coordinately regulated with Brca1 during proliferation and differentiation in mammary epithelial cells. Proceedings of the National Academy of Sciences, 93, 13078–13083.CrossRef Rajan, J. V., Wang, M., Marquis, S. T., & Chodosh, L. A. (1996). Brca2 is coordinately regulated with Brca1 during proliferation and differentiation in mammary epithelial cells. Proceedings of the National Academy of Sciences, 93, 13078–13083.CrossRef
25.
go back to reference Sharan, S. K., Morimatsu, M., Albrecht, U., Lim, D. S., Regel, E., Dinh, C., et al. (1997). Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2. Nature, 386, 804–810.CrossRefPubMed Sharan, S. K., Morimatsu, M., Albrecht, U., Lim, D. S., Regel, E., Dinh, C., et al. (1997). Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2. Nature, 386, 804–810.CrossRefPubMed
26.
go back to reference Marmorstein, L. Y., Ouchi, T., & Stuart, A. A. (1998). The BRCA2 gene product functionally interacts with p53 and RAD51. Proceedings of the National Academy of Sciences of the United States of America, 95(23), 13869–13874.CrossRefPubMed Marmorstein, L. Y., Ouchi, T., & Stuart, A. A. (1998). The BRCA2 gene product functionally interacts with p53 and RAD51. Proceedings of the National Academy of Sciences of the United States of America, 95(23), 13869–13874.CrossRefPubMed
27.
go back to reference Crotser, C. B., & Boehmke, M. (2009). Survivorship considerations in adults with hereditary breast and ovarian cancer syndrome: state of the science. Journal of Cancer Survival, 3(1), 21–42.CrossRef Crotser, C. B., & Boehmke, M. (2009). Survivorship considerations in adults with hereditary breast and ovarian cancer syndrome: state of the science. Journal of Cancer Survival, 3(1), 21–42.CrossRef
28.
go back to reference Russo, A., Calò, V., Bruno, L., Rizzo, S., Bazan, V., & Di Fede, G. (2009). Hereditary ovarian cancer. Critical Reviews in Oncology/Hematology, 69(1), 28–44.CrossRefPubMed Russo, A., Calò, V., Bruno, L., Rizzo, S., Bazan, V., & Di Fede, G. (2009). Hereditary ovarian cancer. Critical Reviews in Oncology/Hematology, 69(1), 28–44.CrossRefPubMed
29.
go back to reference van der Velde, N. M., Mourits, M. J., Arts, H. J., de Vries, J., Leegte, B. K., Dijkhuis, G., et al. (2009). Time to stop ovarian cancer screening in BRCA1/2 mutation carriers? International Journal of Cancer, 124(4), 919–923.CrossRef van der Velde, N. M., Mourits, M. J., Arts, H. J., de Vries, J., Leegte, B. K., Dijkhuis, G., et al. (2009). Time to stop ovarian cancer screening in BRCA1/2 mutation carriers? International Journal of Cancer, 124(4), 919–923.CrossRef
30.
go back to reference Nelson, H. D., Huffman, L. H., Fu, R., & Harris, E. L. (2005). U.S. Preventive Services Task Force. Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility: systematic evidence review for the U.S. Preventive Services Task Force. Annals of Internal Medicine, 143(5), 362–379. Nelson, H. D., Huffman, L. H., Fu, R., & Harris, E. L. (2005). U.S. Preventive Services Task Force. Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility: systematic evidence review for the U.S. Preventive Services Task Force. Annals of Internal Medicine, 143(5), 362–379.
31.
go back to reference Thomassen, M., Hansen, T. V., Borg, A., Lianee, H. T., Wikman, F., Pedersen, I. S., et al. (2007). Hereditary ovarian cancer—assessing risk and prevention strategies. Obstetrics and Gynecology Clinics of North America, 34(4), 651–665.CrossRef Thomassen, M., Hansen, T. V., Borg, A., Lianee, H. T., Wikman, F., Pedersen, I. S., et al. (2007). Hereditary ovarian cancer—assessing risk and prevention strategies. Obstetrics and Gynecology Clinics of North America, 34(4), 651–665.CrossRef
32.
go back to reference Skinner, C. S., Schildkraut, J. M., Berry, D., Calingaert, B., Marcom, P. K., Sugarman, J., et al. (2002). Pre-counseling education materials for BRCA testing: does tailoring make a difference? Genetis Testing, 6(2), 93–105.CrossRef Skinner, C. S., Schildkraut, J. M., Berry, D., Calingaert, B., Marcom, P. K., Sugarman, J., et al. (2002). Pre-counseling education materials for BRCA testing: does tailoring make a difference? Genetis Testing, 6(2), 93–105.CrossRef
33.
go back to reference Peters, N., Domchek, S. M., Rose, A., Polis, R., Stopfer, J., & Armstrong, K. (2005). Knowledge, attitudes, and utilization of BRCA1/2 testing among women with early onset breast cancer. Genet Test, 9(1), 48–53.CrossRefPubMed Peters, N., Domchek, S. M., Rose, A., Polis, R., Stopfer, J., & Armstrong, K. (2005). Knowledge, attitudes, and utilization of BRCA1/2 testing among women with early onset breast cancer. Genet Test, 9(1), 48–53.CrossRefPubMed
34.
go back to reference Vadaparampil, S. T., Wey, J. P., & Kinney, A. Y. (2004). Psychosocial aspects of genetic counseling and testing. Seminars in Oncology Nursing, 20(3), 186–195.CrossRefPubMed Vadaparampil, S. T., Wey, J. P., & Kinney, A. Y. (2004). Psychosocial aspects of genetic counseling and testing. Seminars in Oncology Nursing, 20(3), 186–195.CrossRefPubMed
35.
go back to reference Kehoe, S. M., & Kauff, N. D. (2007). Screening and prevention of hereditary gynecologic cancers. Seminars in Oncology, 34(5), 406–410.CrossRefPubMed Kehoe, S. M., & Kauff, N. D. (2007). Screening and prevention of hereditary gynecologic cancers. Seminars in Oncology, 34(5), 406–410.CrossRefPubMed
36.
go back to reference Lux, M. P., Fasching, P. A., & Beckmann, M. W. (2006). Hereditary breast and ovarian cancer: review and future perspectives. Journal of Molecular Medicine, 84, 16–28.CrossRefPubMed Lux, M. P., Fasching, P. A., & Beckmann, M. W. (2006). Hereditary breast and ovarian cancer: review and future perspectives. Journal of Molecular Medicine, 84, 16–28.CrossRefPubMed
37.
go back to reference De la Hoya, M., Diez, O., Pérez-Segura, P., et al. (2003). Pre-test prediction models of BRCA1 or BRCA2 mutation in breast/ovarian families attending familial cancer clinics. Journal of Medical Genetics, 40, 503–510.CrossRefPubMed De la Hoya, M., Diez, O., Pérez-Segura, P., et al. (2003). Pre-test prediction models of BRCA1 or BRCA2 mutation in breast/ovarian families attending familial cancer clinics. Journal of Medical Genetics, 40, 503–510.CrossRefPubMed
38.
go back to reference Myers, E. R., Havrilesky, L. J., Kulasingam, S. L., Sanders, G. D., Cline, K. E., Gray, R. N., et al. (2006). Genomic tests for ovarian cancer detection and management. Evidence Report/Technology Assessment (full report), 145, 1–100. Myers, E. R., Havrilesky, L. J., Kulasingam, S. L., Sanders, G. D., Cline, K. E., Gray, R. N., et al. (2006). Genomic tests for ovarian cancer detection and management. Evidence Report/Technology Assessment (full report), 145, 1–100.
39.
go back to reference Low, C. A., Bower, J. E., Kwan, L., & Seldon, J. (2008). Benefit finding in response to BRCA1/2 testing. Annals of Behavioral Medicine, 35(1), 61–69.PubMed Low, C. A., Bower, J. E., Kwan, L., & Seldon, J. (2008). Benefit finding in response to BRCA1/2 testing. Annals of Behavioral Medicine, 35(1), 61–69.PubMed
40.
go back to reference Kieran, S., Loescher, L. J., & Lim, K. H. (2007). The role of financial factors in acceptance of clinical BRCA genetic testing. Genetic Testing, 11(1), 101–110.CrossRefPubMed Kieran, S., Loescher, L. J., & Lim, K. H. (2007). The role of financial factors in acceptance of clinical BRCA genetic testing. Genetic Testing, 11(1), 101–110.CrossRefPubMed
41.
go back to reference Herman, L. M. (2008). Clinical and Scientific Affairs Council of the AAPA. Hereditary breast and ovarian cancers. JAAPA, 21(5), 18–21.PubMed Herman, L. M. (2008). Clinical and Scientific Affairs Council of the AAPA. Hereditary breast and ovarian cancers. JAAPA, 21(5), 18–21.PubMed
42.
go back to reference Lacour, R. A., Daniels, M. S., Westin, S. N., Meyer, L. A., Burke, C. C., Burns, K. A., et al. (2008). What women with ovarian cancer think and know about genetic testing. Gynecologic Oncology, 111(1), 132–136.CrossRefPubMed Lacour, R. A., Daniels, M. S., Westin, S. N., Meyer, L. A., Burke, C. C., Burns, K. A., et al. (2008). What women with ovarian cancer think and know about genetic testing. Gynecologic Oncology, 111(1), 132–136.CrossRefPubMed
43.
go back to reference Bakos, A. D., Hutson, S. P., Loud, J. T., Peters, J. A., Giusti, R. M., & Greene, M. H. (2008). BRCA mutation-negative women from hereditary breast and ovarian cancer families: a qualitative study of the BRCA-negative experience. Health Expectations, 11(3), 220–231.CrossRefPubMed Bakos, A. D., Hutson, S. P., Loud, J. T., Peters, J. A., Giusti, R. M., & Greene, M. H. (2008). BRCA mutation-negative women from hereditary breast and ovarian cancer families: a qualitative study of the BRCA-negative experience. Health Expectations, 11(3), 220–231.CrossRefPubMed
44.
go back to reference Fields, M. M., & Chevlen, E. (2006). Ovarian cancer screening: a look at the evidence. Clinical Journal of Oncology Nursing, 10(1), 77–81.CrossRefPubMed Fields, M. M., & Chevlen, E. (2006). Ovarian cancer screening: a look at the evidence. Clinical Journal of Oncology Nursing, 10(1), 77–81.CrossRefPubMed
45.
go back to reference Wakahara, F., Kikkawa, F., Nawa, A., et al. (2001). Diagnostic efficacy of tumor markers, sonography, and intraoperative frozen section for ovarian tumors. Gynecologic and Obstetric Investigation, 52, 147–152.CrossRefPubMed Wakahara, F., Kikkawa, F., Nawa, A., et al. (2001). Diagnostic efficacy of tumor markers, sonography, and intraoperative frozen section for ovarian tumors. Gynecologic and Obstetric Investigation, 52, 147–152.CrossRefPubMed
46.
go back to reference Woodward, E. R., Sleightholme, H. V., Considine, A. M., Williamson, S., McHugo, J. M., & Cruger, D. G. (2007). Annual surveillance by CA125 and transvaginal ultrasound for ovarian cancer in both high-risk and population risk women is ineffective. BJOG, 114(12), 1500–1509.CrossRefPubMed Woodward, E. R., Sleightholme, H. V., Considine, A. M., Williamson, S., McHugo, J. M., & Cruger, D. G. (2007). Annual surveillance by CA125 and transvaginal ultrasound for ovarian cancer in both high-risk and population risk women is ineffective. BJOG, 114(12), 1500–1509.CrossRefPubMed
47.
go back to reference Bermejo-Pérez, M. J., Márquez-Calderón, S., & Llanos-Méndez, A. (2008). Cancer surveillance based on imaging techniques in carriers of BRCA1/2 gene mutations: a systematic review. British Journal of Radiology, 81(963), 172–179.CrossRefPubMed Bermejo-Pérez, M. J., Márquez-Calderón, S., & Llanos-Méndez, A. (2008). Cancer surveillance based on imaging techniques in carriers of BRCA1/2 gene mutations: a systematic review. British Journal of Radiology, 81(963), 172–179.CrossRefPubMed
48.
go back to reference McInerney-Leo, A., Biesecker, B. B., Hadley, D. W., Kase, R. G., Giambarresi, T. R., Johnson, E., et al. (2005). BRCA1/2 testing in hereditary breast and ovarian cancer families II: impact on relationships. American Journal of Medical Genetics, 133A(2), 165–169.CrossRefPubMed McInerney-Leo, A., Biesecker, B. B., Hadley, D. W., Kase, R. G., Giambarresi, T. R., Johnson, E., et al. (2005). BRCA1/2 testing in hereditary breast and ovarian cancer families II: impact on relationships. American Journal of Medical Genetics, 133A(2), 165–169.CrossRefPubMed
49.
go back to reference Lacey, J. V., Jr., Greene, M. H., Buys, S. S., Reding, D., Riley, T. L., Berg, C. D., et al. (2006). Ovarian cancer screening in women with a family history of breast or ovarian cancer. Obstetrics and Gynecology, 108(5), 1176–1184.PubMed Lacey, J. V., Jr., Greene, M. H., Buys, S. S., Reding, D., Riley, T. L., Berg, C. D., et al. (2006). Ovarian cancer screening in women with a family history of breast or ovarian cancer. Obstetrics and Gynecology, 108(5), 1176–1184.PubMed
50.
go back to reference Myers, E. R., Bastian, L. A., Havrilesky, L. J., Kulasingam, S. L., Terplan, M. S., Cline, K. E., et al. (2006). Management of adnexal mass. Evidence Report/Technology Assessment, 130, 1–145.PubMed Myers, E. R., Bastian, L. A., Havrilesky, L. J., Kulasingam, S. L., Terplan, M. S., Cline, K. E., et al. (2006). Management of adnexal mass. Evidence Report/Technology Assessment, 130, 1–145.PubMed
51.
go back to reference Bast, R. C., Jr., Brewer, M., Zou, C., Hernandez, M. A., Daley, M., Ozols, R., et al. (2007). Prevention and early detection of ovarian cancer: mission impossible? Recent Results in Cancer Research, 174, 91–100.CrossRefPubMed Bast, R. C., Jr., Brewer, M., Zou, C., Hernandez, M. A., Daley, M., Ozols, R., et al. (2007). Prevention and early detection of ovarian cancer: mission impossible? Recent Results in Cancer Research, 174, 91–100.CrossRefPubMed
52.
go back to reference Narod, S. A., Sun, P., & Risch, H. A. (2001). Ovarian cancer, oral contraceptives, and BRCA mutations. New England Journal of Medicine, 345, 1706–1707.CrossRefPubMed Narod, S. A., Sun, P., & Risch, H. A. (2001). Ovarian cancer, oral contraceptives, and BRCA mutations. New England Journal of Medicine, 345, 1706–1707.CrossRefPubMed
53.
go back to reference Modan, B., Hartge, P., Hirsh-Yechezkel, G., et al. (2001). Parity, oral contraceptives, and the risk of ovarian cancer among carriers and noncarriers of a BRCA1 or BRCA2 mutation. New England Journal of Medicine, 345, 235–240.CrossRefPubMed Modan, B., Hartge, P., Hirsh-Yechezkel, G., et al. (2001). Parity, oral contraceptives, and the risk of ovarian cancer among carriers and noncarriers of a BRCA1 or BRCA2 mutation. New England Journal of Medicine, 345, 235–240.CrossRefPubMed
54.
go back to reference Sabichi, A. L., Hendricks, D. T., Bober, M. A., & Birrer, M. J. (1998). Retinoic acid receptor beta expression and growth inhibition of gynaecologic cancer cells by the synthetic retinoid N-(4-hydroxyphenyl) retinamide. Journal of the National Cancer Institute, 90, 597–605.CrossRefPubMed Sabichi, A. L., Hendricks, D. T., Bober, M. A., & Birrer, M. J. (1998). Retinoic acid receptor beta expression and growth inhibition of gynaecologic cancer cells by the synthetic retinoid N-(4-hydroxyphenyl) retinamide. Journal of the National Cancer Institute, 90, 597–605.CrossRefPubMed
55.
go back to reference Supino, R., Crosti, M., Clerici, M., et al. (1996). Induction of apoptosis by fenretinide (4HPR) in human ovarian carcinoma cells and its association with retinoic acid receptor expression. International Journal of Cancer, 65, 491–497.CrossRef Supino, R., Crosti, M., Clerici, M., et al. (1996). Induction of apoptosis by fenretinide (4HPR) in human ovarian carcinoma cells and its association with retinoic acid receptor expression. International Journal of Cancer, 65, 491–497.CrossRef
56.
go back to reference Benbrook, D. M., Madler, M. M., Spruce, L. W., Birckbichler, P. J., Nelson, E. C., Subramanian, S., et al. (1997). Biologically active heteroarotinoids exhibiting anticancer activity and decreased toxicity. Journal of Medicinal Chemistry, 40(22), 3567–3583.CrossRefPubMed Benbrook, D. M., Madler, M. M., Spruce, L. W., Birckbichler, P. J., Nelson, E. C., Subramanian, S., et al. (1997). Biologically active heteroarotinoids exhibiting anticancer activity and decreased toxicity. Journal of Medicinal Chemistry, 40(22), 3567–3583.CrossRefPubMed
57.
go back to reference Guruswamy, S., Lightfoot, S., Gold, M. A., Hassan, R., Berlin, K. D., Ivey, R. T., et al. (2001). Effects of retinoids on cancerous phenotype and apoptosis in organotypic cultures of ovarian carcinoma. Journal of the National Cancer Institute, 93, 516–525.CrossRefPubMed Guruswamy, S., Lightfoot, S., Gold, M. A., Hassan, R., Berlin, K. D., Ivey, R. T., et al. (2001). Effects of retinoids on cancerous phenotype and apoptosis in organotypic cultures of ovarian carcinoma. Journal of the National Cancer Institute, 93, 516–525.CrossRefPubMed
58.
go back to reference Lefkowitz, E. S., & Garland, C. F. (1994). Sunlight, vitamin D, and ovarian cancer mortality rates in US women. International Journal of Epidemiology, 23, 1133–1136.CrossRefPubMed Lefkowitz, E. S., & Garland, C. F. (1994). Sunlight, vitamin D, and ovarian cancer mortality rates in US women. International Journal of Epidemiology, 23, 1133–1136.CrossRefPubMed
59.
go back to reference Ahonen, M. H., Zhuang, Y. H., Aine, R., Ylikomi, T., & Tuohimaa, P. (2000). Androgen receptor and vitamin D receptor in human ovarian cancer: growth stimulation and inhibition by ligands. International Journal of Cancer, 86, 40–46.CrossRef Ahonen, M. H., Zhuang, Y. H., Aine, R., Ylikomi, T., & Tuohimaa, P. (2000). Androgen receptor and vitamin D receptor in human ovarian cancer: growth stimulation and inhibition by ligands. International Journal of Cancer, 86, 40–46.CrossRef
60.
go back to reference Ness, R. B., & Cottreau, C. (1999). Possible role of ovarian epithelial inflammation in ovarian cancer. Journal of the National Cancer Institute, 91, 1459–1467.CrossRefPubMed Ness, R. B., & Cottreau, C. (1999). Possible role of ovarian epithelial inflammation in ovarian cancer. Journal of the National Cancer Institute, 91, 1459–1467.CrossRefPubMed
61.
go back to reference Moysich, K. B., Mettlin, C., Piver, M. S., Natarajan, N., Menezes, R. J., & Swede, H. (2001). Regular use of analgesic drugs and ovarian cancer risk. Cancer Epidemiology, Biomarkers and Prevention, 10, 903–906.PubMed Moysich, K. B., Mettlin, C., Piver, M. S., Natarajan, N., Menezes, R. J., & Swede, H. (2001). Regular use of analgesic drugs and ovarian cancer risk. Cancer Epidemiology, Biomarkers and Prevention, 10, 903–906.PubMed
62.
go back to reference Rosenberg, L., Palmer, J. R., Rao, R. S., Coogan, P. F., Strom, B. L., Zauber, A. G., et al. (2000). A case-control study of analgesic use and ovarian cancer. Cancer Epidemiology, Biomarkers and Prevention, 9, 933–937.PubMed Rosenberg, L., Palmer, J. R., Rao, R. S., Coogan, P. F., Strom, B. L., Zauber, A. G., et al. (2000). A case-control study of analgesic use and ovarian cancer. Cancer Epidemiology, Biomarkers and Prevention, 9, 933–937.PubMed
63.
go back to reference Cramer, D. W., Harlow, B. L., Titus-Ernstoff, L., Bohlke, K., Welch, W. R., & Greenberg, E. R. (1998). Over-the-counter analgesics and risk of ovarian cancer. Lancet, 351, 104–107.CrossRefPubMed Cramer, D. W., Harlow, B. L., Titus-Ernstoff, L., Bohlke, K., Welch, W. R., & Greenberg, E. R. (1998). Over-the-counter analgesics and risk of ovarian cancer. Lancet, 351, 104–107.CrossRefPubMed
64.
go back to reference Taketo, M. M. (1998). Cyclooxygenase-2 inhibitors in tumorigenesis (part I). Journal of the National Cancer Institute, 90, 1529–1536.CrossRefPubMed Taketo, M. M. (1998). Cyclooxygenase-2 inhibitors in tumorigenesis (part I). Journal of the National Cancer Institute, 90, 1529–1536.CrossRefPubMed
65.
go back to reference Taketo, M. M. (1998). Cyclooxygenase-2 inhibitors in tumorigenesis (Part II). Journal of the National Cancer Institute, 90, 1609–1620.CrossRefPubMed Taketo, M. M. (1998). Cyclooxygenase-2 inhibitors in tumorigenesis (Part II). Journal of the National Cancer Institute, 90, 1609–1620.CrossRefPubMed
66.
go back to reference Williams, C. S., Mann, M., & DuBois, R. N. (1999). The role of cyclooxygenases in inflammation, cancer, and development. Oncogene, 18, 7908–7916.CrossRefPubMed Williams, C. S., Mann, M., & DuBois, R. N. (1999). The role of cyclooxygenases in inflammation, cancer, and development. Oncogene, 18, 7908–7916.CrossRefPubMed
67.
go back to reference Murphy, G. J., & Holder, J. C. (2000). PPAR-gamma agonists: therapeutic role in diabetes, inflammation and cancer. Trends in Pharmacological Sciences, 21, 469–474.CrossRefPubMed Murphy, G. J., & Holder, J. C. (2000). PPAR-gamma agonists: therapeutic role in diabetes, inflammation and cancer. Trends in Pharmacological Sciences, 21, 469–474.CrossRefPubMed
68.
go back to reference Adams, M., Montague, C. T., Prins, J. B., Holder, J. C., Smith, S. A., Sanders, L., et al. (1997). Activators of peroxisome proliferator-activated receptor gamma have depot-specific effects on human preadipocyte differentiation. Journal of Clinical Investigation, 100, 3149–3153.CrossRefPubMed Adams, M., Montague, C. T., Prins, J. B., Holder, J. C., Smith, S. A., Sanders, L., et al. (1997). Activators of peroxisome proliferator-activated receptor gamma have depot-specific effects on human preadipocyte differentiation. Journal of Clinical Investigation, 100, 3149–3153.CrossRefPubMed
69.
go back to reference Mueller, E., Sarraf, P., Tontonoz, P., Evans, R. M., Martin, K. J., Zhang, M., et al. (1998). Terminal differentiation of human breast cancer through PPAR gamma. Molecular Cell, 1, 465–470.CrossRefPubMed Mueller, E., Sarraf, P., Tontonoz, P., Evans, R. M., Martin, K. J., Zhang, M., et al. (1998). Terminal differentiation of human breast cancer through PPAR gamma. Molecular Cell, 1, 465–470.CrossRefPubMed
70.
go back to reference You, Y. N., Lakhani, V. T., & Wells, S. A., Jr. (2007). The role of prophylactic surgery in cancer prevention. World Journal of Surgery, 31(3), 450–464.CrossRefPubMed You, Y. N., Lakhani, V. T., & Wells, S. A., Jr. (2007). The role of prophylactic surgery in cancer prevention. World Journal of Surgery, 31(3), 450–464.CrossRefPubMed
71.
go back to reference Domchek, S. M., & Rebbeck, T. R. (2007). Prophylactic oophorectomy in women at increased cancer risk. Current Opinion in Obstetrics and Gynecology, 19(1), 27–30.CrossRefPubMed Domchek, S. M., & Rebbeck, T. R. (2007). Prophylactic oophorectomy in women at increased cancer risk. Current Opinion in Obstetrics and Gynecology, 19(1), 27–30.CrossRefPubMed
72.
go back to reference ACOG Practice Bulletin No. 89. (2008). Elective and risk-reducing salpingo-oophorectomy. ObstetriciÂa ginecologiÂa, 111(1), 231–241. ACOG Practice Bulletin No. 89. (2008). Elective and risk-reducing salpingo-oophorectomy. ObstetriciÂa ginecologiÂa, 111(1), 231–241.
73.
go back to reference Guillem, J. G., Wood, W. C., Moley, J. F., Berchuck, A., Karlan, B. Y., Mutch, D. G., et al. (2006). Offit K; ASCO; SSO. ASCO/SSO review of current role of risk-reducing surgery in common hereditary cancer syndromes. Journal of Clinical Oncology, 24(28), 4642–4660.CrossRefPubMed Guillem, J. G., Wood, W. C., Moley, J. F., Berchuck, A., Karlan, B. Y., Mutch, D. G., et al. (2006). Offit K; ASCO; SSO. ASCO/SSO review of current role of risk-reducing surgery in common hereditary cancer syndromes. Journal of Clinical Oncology, 24(28), 4642–4660.CrossRefPubMed
74.
go back to reference Tinelli, A., Malvasi, A., Casciaro, S., Leo, G., Vergara, D., Pisanò, M., et al. (2007). Tailoring minimally invasive gynaecological surgery based on biogenomic findings. In S. Casciaro & B. Gersak (Eds.), New technology frontiers in minimally invasive therapies (pp. 43–62). Italy: Lupiensis Biomedical Publications. 6. Tinelli, A., Malvasi, A., Casciaro, S., Leo, G., Vergara, D., Pisanò, M., et al. (2007). Tailoring minimally invasive gynaecological surgery based on biogenomic findings. In S. Casciaro & B. Gersak (Eds.), New technology frontiers in minimally invasive therapies (pp. 43–62). Italy: Lupiensis Biomedical Publications. 6.
75.
go back to reference Lancaster, J. M., Powell, C. B., Kauff, N. D., Cass, I., Chen, L. M., Lu, K. H., et al. (2007). Society of Gynecologic Oncologists Education Committee statement on risk assessment for inherited gynecologic cancer predispositions. Gynecologic Oncology, 107(2), 159–162.CrossRefPubMed Lancaster, J. M., Powell, C. B., Kauff, N. D., Cass, I., Chen, L. M., Lu, K. H., et al. (2007). Society of Gynecologic Oncologists Education Committee statement on risk assessment for inherited gynecologic cancer predispositions. Gynecologic Oncology, 107(2), 159–162.CrossRefPubMed
76.
go back to reference Batista, L. I., Lu, K. H., Beahm, E. K., Arun, B. K., Bodurka, D. C., & Meric-Bernstam, F. (2008). Coordinated prophylactic surgical management for women with hereditary breast-ovarian cancer syndrome. BMC Cancer, 8, 101.CrossRefPubMed Batista, L. I., Lu, K. H., Beahm, E. K., Arun, B. K., Bodurka, D. C., & Meric-Bernstam, F. (2008). Coordinated prophylactic surgical management for women with hereditary breast-ovarian cancer syndrome. BMC Cancer, 8, 101.CrossRefPubMed
77.
go back to reference Gómez García EB, Oosterwijk JC, Timmermans M, van Asperen CJ, Hogervorst FBL, Hoogerbrugge N, et al. A method to assess the clinical significance of unclassified variants in the BRCA1 and BRCA2 genes based on cancer family history. Breast Cancer Research. 2009;11(1): R8. Gómez García EB, Oosterwijk JC, Timmermans M, van Asperen CJ, Hogervorst FBL, Hoogerbrugge N, et al. A method to assess the clinical significance of unclassified variants in the BRCA1 and BRCA2 genes based on cancer family history. Breast Cancer Research. 2009;11(1): R8.
78.
go back to reference Rebbeck, T. R., Kauff, N. D., & Domchek, S. M. (2009). Meta-analysis of risk reduction estimates associated with risk-reducing salpingo-oophorectomy in BRCA1 or BRCA2 mutation carriers. Journal of the National Cancer Institute, 101(2), 80–87.CrossRefPubMed Rebbeck, T. R., Kauff, N. D., & Domchek, S. M. (2009). Meta-analysis of risk reduction estimates associated with risk-reducing salpingo-oophorectomy in BRCA1 or BRCA2 mutation carriers. Journal of the National Cancer Institute, 101(2), 80–87.CrossRefPubMed
79.
go back to reference Greene, M. H., Piedmonte, M., Alberts, D., Gail, M., Hensley, M., Miner, Z., et al. (2008). A prospective study of risk-reducing salpingo-oophorectomy and longitudinal CA-125 screening among women at increased genetic risk of ovarian cancer: design and baseline characteristics: a Gynecologic Oncology Group study. Cancer Epidemiology, Biomarkers and Prevention, 17(3), 594–604.CrossRefPubMed Greene, M. H., Piedmonte, M., Alberts, D., Gail, M., Hensley, M., Miner, Z., et al. (2008). A prospective study of risk-reducing salpingo-oophorectomy and longitudinal CA-125 screening among women at increased genetic risk of ovarian cancer: design and baseline characteristics: a Gynecologic Oncology Group study. Cancer Epidemiology, Biomarkers and Prevention, 17(3), 594–604.CrossRefPubMed
80.
go back to reference Menon, U., Gentry-Maharaj, A., Hallett, R., Ryan, A., Burnell, M., Sharma, A., et al. (2009). Sensitivity and specificity of multimodal and ultrasound screening for ovarian cancer, and stage distribution of detected cancers: results of the prevalence screen of the UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS). Lancet Oncology, 10(4), 327–340.CrossRefPubMed Menon, U., Gentry-Maharaj, A., Hallett, R., Ryan, A., Burnell, M., Sharma, A., et al. (2009). Sensitivity and specificity of multimodal and ultrasound screening for ovarian cancer, and stage distribution of detected cancers: results of the prevalence screen of the UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS). Lancet Oncology, 10(4), 327–340.CrossRefPubMed
81.
go back to reference Partridge, E., Kreimer, A. R., Greenlee, R. T., Williams, C., Xu, J. L., Church, T. R., et al. (2009). Results from four rounds of ovarian cancer screening in a randomized trial. Obstetrics and Gynecology, 113(4), 775–782.PubMed Partridge, E., Kreimer, A. R., Greenlee, R. T., Williams, C., Xu, J. L., Church, T. R., et al. (2009). Results from four rounds of ovarian cancer screening in a randomized trial. Obstetrics and Gynecology, 113(4), 775–782.PubMed
82.
go back to reference Kurian, A. W., Sigal, B. M., & Plevritis, S. K. (2010). Survival analysis of cancer risk reduction strategies for BRCA1/2 mutation carriers. Journal of Clinical Oncology, 28(2), 222–231.CrossRefPubMed Kurian, A. W., Sigal, B. M., & Plevritis, S. K. (2010). Survival analysis of cancer risk reduction strategies for BRCA1/2 mutation carriers. Journal of Clinical Oncology, 28(2), 222–231.CrossRefPubMed
Metadata
Title
Hereditary ovarian cancers: from BRCA mutations to clinical management. A modern appraisal
Authors
Andrea Tinelli
Antonio Malvasi
Giuseppe Leo
Daniele Vergara
Maurizio Pisanò
Mariangela Ciccarese
Vincenzo Emanuele Chiuri
Vito Lorusso
Publication date
01-06-2010
Publisher
Springer US
Published in
Cancer and Metastasis Reviews / Issue 2/2010
Print ISSN: 0167-7659
Electronic ISSN: 1573-7233
DOI
https://doi.org/10.1007/s10555-010-9218-3

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