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Volumn 20, Issue 3, 2010, Pages 231-238

The inherited genetics of ovarian and endometrial cancer

Author keywords

[No Author keywords available]

Indexed keywords

BRCA1 PROTEIN; BRCA2 PROTEIN; MISMATCH REPAIR PROTEIN; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE;

EID: 77953615401     PISSN: 0959437X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.gde.2010.03.001     Document Type: Review
Times cited : (63)

References (56)
  • 2
    • 0029944173 scopus 로고    scopus 로고
    • A population-based study of endometrial cancer and familial risk in younger women. Cancer and Steroid Hormone Study Group
    • Gruber S.B., Thompson W.D. A population-based study of endometrial cancer and familial risk in younger women. Cancer and Steroid Hormone Study Group. Cancer Epidemiol Biomarkers Prev 1996, 5(6):411-417.
    • (1996) Cancer Epidemiol Biomarkers Prev , vol.5 , Issue.6 , pp. 411-417
    • Gruber, S.B.1    Thompson, W.D.2
  • 4
    • 0026584548 scopus 로고
    • Family history of reproductive cancers and ovarian cancer risk: an Italian case-control study
    • Parazzini F., Negri E., La Vecchia C., Restelli C., Franceschi S. Family history of reproductive cancers and ovarian cancer risk: an Italian case-control study. Am J Epidemiol 1992, 135(1):35-40.
    • (1992) Am J Epidemiol , vol.135 , Issue.1 , pp. 35-40
    • Parazzini, F.1    Negri, E.2    La Vecchia, C.3    Restelli, C.4    Franceschi, S.5
  • 6
    • 61449320520 scopus 로고    scopus 로고
    • Endometrial cancer and Lynch syndrome: clinical and pathologic considerations
    • Meyer L.A., Broaddus R.R., Lu K.H. Endometrial cancer and Lynch syndrome: clinical and pathologic considerations. Cancer Control 2009, 16(1):14-22.
    • (2009) Cancer Control , vol.16 , Issue.1 , pp. 14-22
    • Meyer, L.A.1    Broaddus, R.R.2    Lu, K.H.3
  • 8
    • 0033063711 scopus 로고    scopus 로고
    • New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC
    • Vasen H.F., Watson P., Mecklin J.P., Lynch H.T. New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC. Gastroenterology 1999, 116(6):1453-1456.
    • (1999) Gastroenterology , vol.116 , Issue.6 , pp. 1453-1456
    • Vasen, H.F.1    Watson, P.2    Mecklin, J.P.3    Lynch, H.T.4
  • 9
    • 0035761351 scopus 로고    scopus 로고
    • Cancer risk in mismatch repair gene mutation carriers
    • Watson P., Lynch H.T. Cancer risk in mismatch repair gene mutation carriers. Fam Cancer 2001, 1:57-60.
    • (2001) Fam Cancer , vol.1 , pp. 57-60
    • Watson, P.1    Lynch, H.T.2
  • 12
    • 24144484905 scopus 로고    scopus 로고
    • The incidence of Lynch syndrome
    • de la Chapelle A. The incidence of Lynch syndrome. Fam Cancer 2005, 4:233-237.
    • (2005) Fam Cancer , vol.4 , pp. 233-237
    • de la Chapelle, A.1
  • 14
    • 33646408125 scopus 로고    scopus 로고
    • The contribution of the hereditary non polyposis colorectal cancer syndrome to the development of ovarian cancer
    • Malander S., Rambech E., Kristoffersson U., Halvarsson B., Ridderheim M., Borg A., Nilbert M. The contribution of the hereditary non polyposis colorectal cancer syndrome to the development of ovarian cancer. Gynecol Oncol 2006, 101:238-243.
    • (2006) Gynecol Oncol , vol.101 , pp. 238-243
    • Malander, S.1    Rambech, E.2    Kristoffersson, U.3    Halvarsson, B.4    Ridderheim, M.5    Borg, A.6    Nilbert, M.7
  • 15
    • 0031958466 scopus 로고    scopus 로고
    • BRCA1, BRCA2, and hereditary non polyposis colorectal cancer gene mutations in an unselected ovarian cancer population: relationship to family history and implications for genetic testing
    • Rubin S.C., Blackwood M.A., Bandera C., Behbakht K., Benjamin I., Rebbeck T.R., Boyd J. BRCA1, BRCA2, and hereditary non polyposis colorectal cancer gene mutations in an unselected ovarian cancer population: relationship to family history and implications for genetic testing. Am J Obstet Gynecol 1998, 178:670-677.
    • (1998) Am J Obstet Gynecol , vol.178 , pp. 670-677
    • Rubin, S.C.1    Blackwood, M.A.2    Bandera, C.3    Behbakht, K.4    Benjamin, I.5    Rebbeck, T.R.6    Boyd, J.7
  • 19
    • 0033738748 scopus 로고    scopus 로고
    • Will the real Cowden syndrome please stand up: revised diagnostic criteria
    • Eng C. Will the real Cowden syndrome please stand up: revised diagnostic criteria. J Med Genet 2000, 37:828-830.
    • (2000) J Med Genet , vol.37 , pp. 828-830
    • Eng, C.1
  • 20
    • 0033551070 scopus 로고    scopus 로고
    • New insights into tumor suppression: PTEN suppresses tumor formation by restraining the phosphoinositide 3-kinase/AKT pathway
    • Cantley L.C., Neel B.G. New insights into tumor suppression: PTEN suppresses tumor formation by restraining the phosphoinositide 3-kinase/AKT pathway. Proc Natl Acad Sci U S A 1999, 96:4240-4245.
    • (1999) Proc Natl Acad Sci U S A , vol.96 , pp. 4240-4245
    • Cantley, L.C.1    Neel, B.G.2
  • 22
  • 24
    • 0033365227 scopus 로고    scopus 로고
    • The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes
    • Gayther S.A., Russell P., Harrington P., Antoniou A., Easton D.F., Ponder B.A.J. The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes. Am J Hum Genet 1999, 65:1021-1029.
    • (1999) Am J Hum Genet , vol.65 , pp. 1021-1029
    • Gayther, S.A.1    Russell, P.2    Harrington, P.3    Antoniou, A.4    Easton, D.F.5    Ponder, B.A.J.6
  • 26
    • 63549126247 scopus 로고    scopus 로고
    • The contribution of BRCA1 and BRCA2 to ovarian cancer
    • Ramus S.J., Gayther S.A. The contribution of BRCA1 and BRCA2 to ovarian cancer. Mol Oncol 2009, 3(2):138-150.
    • (2009) Mol Oncol , vol.3 , Issue.2 , pp. 138-150
    • Ramus, S.J.1    Gayther, S.A.2
  • 27
    • 0038744296 scopus 로고    scopus 로고
    • Average risks of breast and ovarian cancer associated with mutations in BRCA1 or BRCA2 detected in case series unselected for family history: a combined analysis of 22 studies
    • Antoniou A., Pharoah P., Narod S., Risch H., Eyfjord J., Hopper J., Loman N., Olsson H., Johannsson O., Borg A., et al. Average risks of breast and ovarian cancer associated with mutations in BRCA1 or BRCA2 detected in case series unselected for family history: a combined analysis of 22 studies. Am J Hum Genet 2003, 72:1117-1131.
    • (2003) Am J Hum Genet , vol.72 , pp. 1117-1131
    • Antoniou, A.1    Pharoah, P.2    Narod, S.3    Risch, H.4    Eyfjord, J.5    Hopper, J.6    Loman, N.7    Olsson, H.8    Johannsson, O.9    Borg, A.10
  • 30
    • 33646446067 scopus 로고    scopus 로고
    • Risk prediction models for familial breast cancer
    • Antoniou A.C., Easton D.F. Risk prediction models for familial breast cancer. Future Oncol 2006, 2(2):257-274.
    • (2006) Future Oncol , vol.2 , Issue.2 , pp. 257-274
    • Antoniou, A.C.1    Easton, D.F.2
  • 31
    • 38549127886 scopus 로고    scopus 로고
    • Progesterone receptor variation and risk of ovarian cancer is limited to the invasive endometrioid subtype: results from the ovarian cancer association consortium pooled analysis
    • Pearce C.L., Wu A.H., Gayther S.A., Bale A.E., Beck P.A., Beesley J., Chanock S., Cramer D.W., Dicioccio R., Edwards R., et al. Progesterone receptor variation and risk of ovarian cancer is limited to the invasive endometrioid subtype: results from the ovarian cancer association consortium pooled analysis. Br J Cancer 2008, 98(2):282-288.
    • (2008) Br J Cancer , vol.98 , Issue.2 , pp. 282-288
    • Pearce, C.L.1    Wu, A.H.2    Gayther, S.A.3    Bale, A.E.4    Beck, P.A.5    Beesley, J.6    Chanock, S.7    Cramer, D.W.8    Dicioccio, R.9    Edwards, R.10
  • 36
    • 58149357365 scopus 로고    scopus 로고
    • Genome-wide association studies in cancer
    • R2
    • Easton D.F., Eeles R.A. Genome-wide association studies in cancer. Hum Mol Genet 2008, 17(R2):R109-R115.
    • (2008) Hum Mol Genet , vol.17
    • Easton, D.F.1    Eeles, R.A.2
  • 37
    • 84934438988 scopus 로고    scopus 로고
    • Role of genetic polymorphisms in ovarian cancer susceptibility: development of an international ovarian cancer association consortium
    • Berchuck A., Schildkraut J.M., Pearce C.L., Chenevix-Trench G., Pharoah P.D. Role of genetic polymorphisms in ovarian cancer susceptibility: development of an international ovarian cancer association consortium. Adv Exp Med Biol 2008, 622:53-67.
    • (2008) Adv Exp Med Biol , vol.622 , pp. 53-67
    • Berchuck, A.1    Schildkraut, J.M.2    Pearce, C.L.3    Chenevix-Trench, G.4    Pharoah, P.D.5
  • 41
    • 34447314503 scopus 로고    scopus 로고
    • Ovarian cancer at young age: the contribution of mismatch-repair defects in a population-based series of epithelial ovarian cancer before age 40
    • Domanska K., Malander S., Masback A., Nilbert M. Ovarian cancer at young age: the contribution of mismatch-repair defects in a population-based series of epithelial ovarian cancer before age 40. Int J Gynecol Cancer 2007, 17(4):789-793.
    • (2007) Int J Gynecol Cancer , vol.17 , Issue.4 , pp. 789-793
    • Domanska, K.1    Malander, S.2    Masback, A.3    Nilbert, M.4
  • 42
    • 0037439957 scopus 로고    scopus 로고
    • BRCA1/2 mutation status influences somatic genetic progression in inherited and sporadic epithelial ovarian cancer cases
    • Ramus S.J., Pharoah P.D., Harrington P., Pye C., Werness B., Bobrow L., Ayhan A., Wells D., Fishman A., Gore M., et al. BRCA1/2 mutation status influences somatic genetic progression in inherited and sporadic epithelial ovarian cancer cases. Cancer Res 2003, 63(2):417-423.
    • (2003) Cancer Res , vol.63 , Issue.2 , pp. 417-423
    • Ramus, S.J.1    Pharoah, P.D.2    Harrington, P.3    Pye, C.4    Werness, B.5    Bobrow, L.6    Ayhan, A.7    Wells, D.8    Fishman, A.9    Gore, M.10
  • 44
    • 47149086213 scopus 로고    scopus 로고
    • Predicting the likelihood of carrying a BRCA1 or BRCA2 mutation: validation of BOADICEA, BRCAPRO, IBIS, Myriad and the Manchester scoring system using data from UK genetics clinics
    • July (7)
    • Antoniou A.C., Hardy R., Walker L., Evans D.G., Shenton A., Eeles R., Shanley S., Pichert G., Izatt L., Rose S., et al. Predicting the likelihood of carrying a BRCA1 or BRCA2 mutation: validation of BOADICEA, BRCAPRO, IBIS, Myriad and the Manchester scoring system using data from UK genetics clinics. J Med Genet 2008, 45(July (7)):425-431.
    • (2008) J Med Genet , vol.45 , pp. 425-431
    • Antoniou, A.C.1    Hardy, R.2    Walker, L.3    Evans, D.G.4    Shenton, A.5    Eeles, R.6    Shanley, S.7    Pichert, G.8    Izatt, L.9    Rose, S.10
  • 46
    • 77953621019 scopus 로고    scopus 로고
    • Risk quantifi{ligature}cation for carrying mutations in Lynch syndrome genes. In ASCO Educational Book 2008;
    • Balmana J, Steyerberg EW, Syngal S: Risk quantifi{ligature}cation for carrying mutations in Lynch syndrome genes. In ASCO Educational Book 2008; 2008:59-64. http://edbook.ascopubs.org/cgi/content/abstract/2008/1/59.
    • (2008) , pp. 59-64
    • Balmana, J.1    Steyerberg, E.W.2    Syngal, S.3
  • 47
    • 45949085378 scopus 로고    scopus 로고
    • Polygenes, risk prediction, and targeted prevention of breast cancer
    • Pharoah P.D., Antoniou A.C., Easton D.F., Ponder B.A. Polygenes, risk prediction, and targeted prevention of breast cancer. N Engl J Med 2008, 358(26):2796-2803.
    • (2008) N Engl J Med , vol.358 , Issue.26 , pp. 2796-2803
    • Pharoah, P.D.1    Antoniou, A.C.2    Easton, D.F.3    Ponder, B.A.4
  • 49
    • 63149087256 scopus 로고    scopus 로고
    • 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)
    • April (4)
    • Menon U., Gentry-Maharaj A., Hallett R., Ryan A., Burnell M., Sharma A., Lewis S., Davies S., Philpott S., Lopes A., et al. 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 Oncol. 2009, 10(April (4)):327-340.
    • (2009) Lancet Oncol. , vol.10 , pp. 327-340
    • Menon, U.1    Gentry-Maharaj, A.2    Hallett, R.3    Ryan, A.4    Burnell, M.5    Sharma, A.6    Lewis, S.7    Davies, S.8    Philpott, S.9    Lopes, A.10


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