메뉴 건너뛰기




Volumn 99, Issue 9, 2008, Pages 1715-1719

Molecular epidemiological and mutational analysis of DNA mismatch repair (MMR) genes in endometrial cancer patients with HNPCC-associated familial predisposition to cancer

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN MLH1; PROTEIN MSH2; PROTEIN MSH6;

EID: 50149105001     PISSN: 13479032     EISSN: 13497006     Source Type: Journal    
DOI: 10.1111/j.1349-7006.2008.00886.x     Document Type: Review
Times cited : (17)

References (33)
  • 1
    • 0015016127 scopus 로고
    • The cancer family syndrome and cancer control
    • Lynch HT, Krush AJ. The cancer family syndrome and cancer control. Surg Gynecol Obstet 1971; 132: 247-250.
    • (1971) Surg Gynecol Obstet , vol.132 , pp. 247-250
    • Lynch, H.T.1    Krush, A.J.2
  • 2
    • 0034065483 scopus 로고    scopus 로고
    • Hereditary nonpolyposis colorectal cancer
    • Lynch HT, Lynch JF. Hereditary nonpolyposis colorectal cancer. Semin Surg Oncol 2000; 18: 305-13.
    • (2000) Semin Surg Oncol , vol.18 , pp. 305-313
    • Lynch, H.T.1    Lynch, J.F.2
  • 3
    • 0025848680 scopus 로고
    • The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer
    • Vasen HF, Mecklin JP, Khan PM et al. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer. Dis Colon Rectum 1991; 34: 424-5.
    • (1991) Dis Colon Rectum , vol.34 , pp. 424-425
    • Vasen, H.F.1    Mecklin, J.P.2    Khan, P.M.3
  • 4
    • 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 HF, Watson P, Mecklin JP et al. New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative Group on HNPCC. Gastroenterology 1999; 116: 1453-6.
    • (1999) Gastroenterology , vol.116 , pp. 1453-1456
    • Vasen, H.F.1    Watson, P.2    Mecklin, J.P.3
  • 5
    • 4644262947 scopus 로고    scopus 로고
    • Association of HNPCC and endometrial cancers
    • Banno K, Susumu N, Yanokura M et al. Association of HNPCC and endometrial cancers. Int J Clin Oncol 2004; 9: 262-9.
    • (2004) Int J Clin Oncol , vol.9 , pp. 262-269
    • Banno, K.1    Susumu, N.2    Yanokura, M.3
  • 6
    • 4644262604 scopus 로고    scopus 로고
    • HNPCC and endometrial cancer
    • Banno K, Susumu N, Hirao T et al. HNPCC and endometrial cancer. J Fam Tumor 2003; 3: 362-67.
    • (2003) J Fam Tumor , vol.3 , pp. 362-367
    • Banno, K.1    Susumu, N.2    Hirao, T.3
  • 7
    • 0029066689 scopus 로고
    • Inactivation of the type I1 TGF-beta receptor in colon cancer cells with microsatellite instability
    • Markowitz S, Wang J, Myeroff L et al. Inactivation of the type I1 TGF-beta receptor in colon cancer cells with microsatellite instability. Science 1995; 268: 1336-8.
    • (1995) Science , vol.268 , pp. 1336-1338
    • Markowitz, S.1    Wang, J.2    Myeroff, L.3
  • 8
    • 0031018674 scopus 로고    scopus 로고
    • Somatic frameshift mutation in the BAX gene in colon cancers of the microsatellite mutator phenotype
    • Rompino N, Yamamoto H, lonov Y et al. Somatic frameshift mutation in the BAX gene in colon cancers of the microsatellite mutator phenotype. Science 1997; 275: 967-9.
    • (1997) Science , vol.275 , pp. 967-969
    • Rompino, N.1    Yamamoto, H.2    Lonov, Y.3
  • 9
    • 0034785885 scopus 로고    scopus 로고
    • Somatic mutations of the PTEN/NMAC1 gene associated with frequent chromosomal loss detected using comparative genomic hybridization in endometrial cancer
    • Hirai Y, Tanaka N, Furuta R, Kawaguchi T, Sakamoto M, Shirahama S, Noda T. Somatic mutations of the PTEN/NMAC1 gene associated with frequent chromosomal loss detected using comparative genomic hybridization in endometrial cancer. Gynecol Oncol 2001; 83 (1): 81-8.
    • (2001) Gynecol Oncol , vol.83 , Issue.1 , pp. 81-88
    • Hirai, Y.1    Tanaka, N.2    Furuta, R.3    Kawaguchi, T.4    Sakamoto, M.5    Shirahama, S.6    Noda, T.7
  • 10
    • 0032520066 scopus 로고    scopus 로고
    • Close correlation between mutation of E2F and hMSH3 genes in colorectal cancers with microsatellite instability
    • Ikeda M, Orimo H, Moriyama H et al. Close correlation between mutation of E2F and hMSH3 genes in colorectal cancers with microsatellite instability. Cancer Res 1998; 58: 594-8.
    • (1998) Cancer Res , vol.58 , pp. 594-598
    • Ikeda, M.1    Orimo, H.2    Moriyama, H.3
  • 11
    • 14444280359 scopus 로고    scopus 로고
    • Frequent mutation of the E2F-4 cell cycle gene in primary human gastrointestinal tumors
    • Souza RF, Yin J, Smolinski KN et al. Frequent mutation of the E2F-4 cell cycle gene in primary human gastrointestinal tumors. Cancer Res 1997; 52: 2350-3.
    • (1997) Cancer Res , vol.52 , pp. 2350-2353
    • Souza, R.F.1    Yin, J.2    Smolinski, K.N.3
  • 12
    • 0033198994 scopus 로고    scopus 로고
    • Frequent frameshift mutations of the TCF-4 gene in colorectal cancers with microsatellite instability
    • Duval A, Gayet J, Zhou XP et al. Frequent frameshift mutations of the TCF-4 gene in colorectal cancers with microsatellite instability. Cancer Res 1999; 59: 4213-15.
    • (1999) Cancer Res , vol.59 , pp. 4213-4215
    • Duval, A.1    Gayet, J.2    Zhou, X.P.3
  • 13
    • 50149090153 scopus 로고    scopus 로고
    • Germline mutation analysis of DNA mismatch repair (MMR) gene in endometrial cancer patients with familial predisposition to cancer; presented in The 2nd Biennial Scientific Meeting of International Society for Gastrointestinal Hereditary Tumours
    • Banno K, Hirai Y, Suzuk M et al. Germline mutation analysis of DNA mismatch repair (MMR) gene in endometrial cancer patients with familial predisposition to cancer; presented in The 2nd Biennial Scientific Meeting of International Society for Gastrointestinal Hereditary Tumours. Iwama T; Familial Cancer 2007; 6: 325-407.
    • (2007) Iwama T; Familial Cancer , vol.6 , pp. 325-407
    • Banno, K.1    Hirai, Y.2    Suzuk, M.3
  • 14
    • 0033855479 scopus 로고    scopus 로고
    • Somatic frameshift alterations in mononucleotide repeat-coating genes in different tumor types from an HNPCC family with germline MSH2 mutation
    • Planck M, Wenngem E, Borg A et al. Somatic frameshift alterations in mononucleotide repeat-coating genes in different tumor types from an HNPCC family with germline MSH2 mutation. Genes Chromosom Cancer 2000; 29: 33-9.
    • (2000) Genes Chromosom Cancer , vol.29 , pp. 33-39
    • Planck, M.1    Wenngem, E.2    Borg, A.3
  • 15
    • 0027248156 scopus 로고
    • Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer
    • Lynch HT, Smyrk TC, Watson P et al. Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer. Gastroenterology 1993; 104: 1535-49.
    • (1993) Gastroenterology , vol.104 , pp. 1535-1549
    • Lynch, H.T.1    Smyrk, T.C.2    Watson, P.3
  • 16
    • 0345050350 scopus 로고    scopus 로고
    • DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer
    • Nystrom-Lahti M, Wu Y, Moisio AL et al. DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer. Hum Mol Genet 1996; 5: 763-9.
    • (1996) Hum Mol Genet , vol.5 , pp. 763-769
    • Nystrom-Lahti, M.1    Wu, Y.2    Moisio, A.L.3
  • 17
    • 10144250305 scopus 로고    scopus 로고
    • Microsatellite instability and mutation analysis of hMSH2 and hMLHI in patients with sporadic, familial and hereditary colorectal cancer
    • Moslein G, Tester DJ, Lindor NM et al. Microsatellite instability and mutation analysis of hMSH2 and hMLHI in patients with sporadic, familial and hereditary colorectal cancer. Hum Mol Genet 1996; 5: 1245-52.
    • (1996) Hum Mol Genet , vol.5 , pp. 1245-1252
    • Moslein, G.1    Tester, D.J.2    Lindor, N.M.3
  • 18
    • 0342872001 scopus 로고    scopus 로고
    • MSH2 and MLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis
    • Wu Y, Nystrom-Lahti M, Osinga J. MSH2 and MLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis. Genes Chromosom Cancer 1997; 18: 269-78.
    • (1997) Genes Chromosom Cancer , vol.18 , pp. 269-278
    • Wu, Y.1    Nystrom-Lahti, M.2    Osinga, J.3
  • 19
    • 0031015440 scopus 로고    scopus 로고
    • Mutations in MLHl are more frequent than in MSH2 in sporadic colorectal cancers with microsatellite instability
    • Herfarth K, Kodner IJ, Whelan AJ. Mutations in MLHl are more frequent than in MSH2 in sporadic colorectal cancers with microsatellite instability. Genes Chromosom Cancer 1997; 18: 42-9.
    • (1997) Genes Chromosom Cancer , vol.18 , pp. 42-49
    • Herfarth, K.1    Kodner, I.J.2    Whelan, A.J.3
  • 20
    • 0031916753 scopus 로고    scopus 로고
    • MLH1 and MSH2 constitutional mutations & colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancer
    • Genuardi M, Anti M, Capozzi E et al. MLH1 and MSH2 constitutional mutations & colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancer. Int J Cancer 1998; 75: 835-9.
    • (1998) Int J Cancer , vol.75 , pp. 835-839
    • Genuardi, M.1    Anti, M.2    Capozzi, E.3
  • 21
    • 0034728794 scopus 로고    scopus 로고
    • Enhanced detection of deleterious and other gerrnline mutations of hMSH2 and hMLH1 in Japanese hereditary nonpolyposis colorectal kindreds
    • Nomura S, Sugano K, Kashiwabara H et al. Enhanced detection of deleterious and other gerrnline mutations of hMSH2 and hMLH1 in Japanese hereditary nonpolyposis colorectal kindreds. Biochem Biophys Res Commun 2000; 271: 120-9.
    • (2000) Biochem Biophys Res Commun , vol.271 , pp. 120-129
    • Nomura, S.1    Sugano, K.2    Kashiwabara, H.3
  • 22
    • 0028308161 scopus 로고
    • Frequent replication errors at microsatellite loci in tumors of patients with multiple primary cancers
    • Horii A, Han HJ, Shimada M et al. Frequent replication errors at microsatellite loci in tumors of patients with multiple primary cancers. Cancer Res 1994; 54: 3373-5.
    • (1994) Cancer Res , vol.54 , pp. 3373-3375
    • Horii, A.1    Han, H.J.2    Shimada, M.3
  • 23
    • 0029904811 scopus 로고    scopus 로고
    • The role of DNA mismatch repair in platinum drug resistance
    • Fink D, Nebel S, Aebi S et al. The role of DNA mismatch repair in platinum drug resistance. Cancer Res 1996; 56: 4881-6.
    • (1996) Cancer Res , vol.56 , pp. 4881-4886
    • Fink, D.1    Nebel, S.2    Aebi, S.3
  • 24
    • 0028034537 scopus 로고
    • The tumor spectrum in HNPCC
    • Watson P, Lynch HT. The tumor spectrum in HNPCC. Anticancer Res 1994; 14: 1640-53.
    • (1994) Anticancer Res , vol.14 , pp. 1640-1653
    • Watson, P.1    Lynch, H.T.2
  • 25
    • 1642633537 scopus 로고    scopus 로고
    • Muir-Torre phenotype has a frequency of DNA mismatch-repair gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam Criteria
    • Kurse R, Rutten A, Lamberti C et al. Muir-Torre phenotype has a frequency of DNA mismatch-repair gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam Criteria. Am J Hum Genet 1998; 63: 63-70.
    • (1998) Am J Hum Genet , vol.63 , pp. 63-70
    • Kurse, R.1    Rutten, A.2    Lamberti, C.3
  • 26
    • 0029775147 scopus 로고    scopus 로고
    • The genetic basis of Muir-Torre syndrome includes hMLH1 locus
    • Bapat B, Xia L, Mandlensky L et al. The genetic basis of Muir-Torre syndrome includes hMLH1 locus. Am J Hum Genet 1996; 59: 763-9.
    • (1996) Am J Hum Genet , vol.59 , pp. 763-769
    • Bapat, B.1    Xia, L.2    Mandlensky, L.3
  • 27
    • 4243102952 scopus 로고    scopus 로고
    • Two Japanese kindreds with endometrial cancer meeting new clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC), Amsterdam Criteria II
    • Banno K, Susumu N, Hirao T et al. Two Japanese kindreds with endometrial cancer meeting new clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC), Amsterdam Criteria II. J Obstet Gynaecol Res 2004; 30 (4): 287-92.
    • (2004) J Obstet Gynaecol Res , vol.30 , Issue.4 , pp. 287-292
    • Banno, K.1    Susumu, N.2    Hirao, T.3
  • 28
    • 0029944173 scopus 로고    scopus 로고
    • A population-based study of endometrial cancer and familial risk in younger women
    • Gruber SB, Thompson WD. A population-based study of endometrial cancer and familial risk in younger women. Cancer Steroid Hormone Study Group Cancer Epidemiol Biomarkers Prev 1996; 5: 411-17.
    • (1996) Epidemiol Biomarkers Prev , vol.5 , pp. 411-417
    • Gruber, S.B.1    Thompson, W.D.2
  • 29
    • 0031893552 scopus 로고    scopus 로고
    • Familial endometrial adenocarcinoma
    • Sandles LG. Familial endometrial adenocarcinoma. Clin Obstet Gynecol 1998; 41: 167-71.
    • (1998) Clin Obstet Gynecol , vol.41 , pp. 167-171
    • Sandles, L.G.1
  • 30
    • 23044501891 scopus 로고    scopus 로고
    • Molecular analysis of familial endometrial carcinoma: A manifestation of hereditary nonpolyposis colorectal cancer or a separate syndrome?
    • Ollikainen M, Abdel-Rahman WM, Moisio AL et al. Molecular analysis of familial endometrial carcinoma: A manifestation of hereditary nonpolyposis colorectal cancer or a separate syndrome? J Clin Oncol 2005; 23 (21): 4609-16.
    • (2005) J Clin Oncol , vol.23 , Issue.21 , pp. 4609-4616
    • Ollikainen, M.1    Abdel-Rahman, W.M.2    Moisio, A.L.3
  • 31
    • 33747892726 scopus 로고    scopus 로고
    • MLH3 mutation in endometrial cancer
    • Taylor NP, Powell MA, Gibb RK et al. MLH3 mutation in endometrial cancer. Cancer Res 2006; 66 (15): 7502-8.
    • (2006) Cancer Res , vol.66 , Issue.15 , pp. 7502-7508
    • Taylor, N.P.1    Powell, M.A.2    Gibb, R.K.3
  • 32
    • 0141565164 scopus 로고    scopus 로고
    • Identification of gennline MSH2 gene mutations in endometrial cancer not fulfilling the new clinical criteria for hereditary nonpolyposis colorectal cancer
    • Banno K, Susumu N, Hirao T et al. Identification of gennline MSH2 gene mutations in endometrial cancer not fulfilling the new clinical criteria for hereditary nonpolyposis colorectal cancer. Cancer Genet Cytogenet 2003; 146: 58-65.
    • (2003) Cancer Genet Cytogenet , vol.146 , pp. 58-65
    • Banno, K.1    Susumu, N.2    Hirao, T.3
  • 33
    • 2442424419 scopus 로고    scopus 로고
    • Germline epimutation of MLH1 in individuals with multiple cancers
    • Suter CM, Martin DI, Ward RL. Germline epimutation of MLH1 in individuals with multiple cancers. Nat Genet 2004; 36 (5): 497-501.
    • (2004) Nat Genet , vol.36 , Issue.5 , pp. 497-501
    • Suter, C.M.1    Martin, D.I.2    Ward, R.L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.