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

被引:23
|
作者
Hirai, Y. [1 ,2 ]
Banno, K. [3 ]
Suzuki, M. [4 ]
Ichikawa, Y. [5 ]
Udagawa, Y. [6 ]
Sugano, K. [7 ]
Miki, Y. [8 ]
机构
[1] Japanese Fdn Canc Res, Inst Canc, Hosp Ariake, Dept Cytol,Koto Ku, Tokyo 1358550, Japan
[2] Japanese Fdn Canc Res, Inst Canc, Hosp Ariake, Dept Gynecol,Koto Ku, Tokyo 1358550, Japan
[3] Keio Univ, Dept Obstet & Gynecol, Fac Med, Tokyo 1608582, Japan
[4] Jichi Med Univ, Dept Obstet & Gynecol, Fac Med, Shimonoshi, Tochigi 3290498, Japan
[5] Kasumigaura Med Ctr, Dept Obstet & Gynecol, Tsuchiura, Ibaragi 3008585, Japan
[6] Fujita Hlth Univ, Dept Obstet & Gynecol, Fac Med, Aichi 4701192, Japan
[7] Tochigi Canc Ctr, Oncogene Res Lab, Utsunomiya, Tochigi 3200834, Japan
[8] Japanese Fdn Canc Res, Inst Canc, Dept Dent Diag, Koto Ku, Tokyo 1358550, Japan
关键词
D O I
10.1111/j.1349-7006.2008.00886.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recently, a high rate of endometrial cancer has been reported in women with hereditary non-polyposis colorectal cancer (HNPCC), suggesting a relationship between familial endometrial cancers and HNPCC. Familial endometrial cancers constitute only about 0.5% of all endometrial carcinomas and it is essential to examine family histories in detail. A mutational analysis of three DNA mismatch repair (MMR) genes (hMLH1, hMSH2 and hMSH6) in patients with endometrial cancer who meet our criteria for familial predisposition to HNPCC-associated endometrial cancers was performed. Mutations were detected in 18 of the 120 patients (15.0%). Most HNPCC-related endometrial cancers do not meet the New Amsterdam Criteria for HNPCC. These clinical criteria may identify only some HNPCC-associated endometrial cancers. Establishing the correct family history for endometrial cancer patients is important for diagnosing familial endometrial carcinomas. An analysis of MMR genes may be useful for patients with endometrial cancer showing familial aggregation. In addition, gynecologists must be accurately informed, and it is important to perform large-scale, multicenter studies both nationwide and internationally.
引用
收藏
页码:1715 / 1719
页数:5
相关论文
共 50 条
  • [31] CLINICAL AND PATHOLOGICAL FEATURES OF ENDOMETRIAL CANCER PATIENTS WITH DNA MISMATCH REPAIR DEFICIENCY TREATED AT A BRAZILIAN CANCER HOSPITAL
    Mayerhoff, E.
    Anton, C.
    Wagner, M.
    Carvalho, J.
    INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2021, 31 : A83 - A84
  • [32] Comparative sequencing study of mismatch repair and homology-directed repair genes in endometrial cancer and breast cancer patients from Kazakhstan
    Zheng, Ying
    Vdovichenko, Natalia
    Schuermann, Peter
    Ramachandran, Dhanya
    Geffers, Robert
    Speith, Lisa-Marie
    Bogdanova, Natalia
    Enssen, Julia
    Dubrowinskaja, Natalia
    Yugay, Tatyana
    Yessimsiitova, Zura Berkutovna
    Turmanov, Nurzhan
    Hillemanns, Peter
    Doerk, Thilo
    INTERNATIONAL JOURNAL OF CANCER, 2025, 156 (04) : 764 - 775
  • [33] Comparative sequencing study of mismatch repair and homology-directed repair genes in endometrial cancer and breast cancer patients from Kazakhstan
    Zheng, Ying
    Vdovichenko, Natalia
    Schuermann, Peter
    Ramachandran, Dhanya
    Robert, Geffers
    Speith, Lisa-Marie
    Bogdanova, Natalia
    Enssen, Julia
    Dubrowinskaja, Natalia
    Yugai, Tatyana
    Yessimsiitova, Zura Berkutovna
    Turmanov, Nurzhan
    Hillemanns, Peter
    Doerk, Thilo
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 1261 - 1261
  • [34] PATIENT-DERIVED ORGANOID MODEL FOR PREDICTION OF MMR (MISMATCH REPAIR) GENE FUNCTION AND CANCER RISK IN PATIENTS WITH GERMLINE VARIATIONS OF MMR GENES
    Kim, Tae Il
    Shin, Youmi
    Seo, Yoojeong
    Kim, Dong Keon
    GASTROENTEROLOGY, 2024, 166 (05) : S375 - S375
  • [35] Mean age of tumor onset in hereditary nonpolyposis colorectal cancer (HNPCC) families correlates with the presence of mutations in DNA mismatch repair genes
    Pensotti, V
    Radice, P
    Presciuttini, S
    Calistri, D
    Gazzoli, I
    Perez, APG
    Mondini, P
    Buonsanti, G
    Sala, P
    Rossetti, C
    Ranzani, GN
    Bertario, L
    Pierotti, MA
    GENES CHROMOSOMES & CANCER, 1997, 19 (03): : 135 - 142
  • [36] Mutational analysis of transforming growth factor β receptor type II and DNA mismatch repair genes in sporadic endometrial carcinomas with microsatellite instability
    Ohwada, M
    Suzuki, M
    Saga, Y
    Suzuki, T
    Ikeda, M
    Yamada, M
    Sato, I
    ONCOLOGY REPORTS, 2000, 7 (04) : 789 - 792
  • [37] DNA repair genes implicated in triple negative familial non-BRCA1/2 breast cancer predisposition
    Ollier, Marie
    Radosevic-Robin, Nina
    Kwiatkowski, Fabrice
    Ponelle, Flora
    Viala, Sandrine
    Privat, Maud
    Uhrhammer, Nancy
    Bernard-Gallon, Dominique
    Penault-Llorca, Frederique
    Bignon, Yves-Jean
    Bidet, Yannick
    AMERICAN JOURNAL OF CANCER RESEARCH, 2015, 5 (07): : 2113 - +
  • [38] Endometrial cancer risk is associated with variants of the mismatch repair genes MLH1 and MSH2
    Beiner, Mario E.
    Rosen, Barry
    Fyles, Anthony
    Harley, Ian
    Pal, Tuya
    Siminovitch, Kathy
    Zhang, Shiyu
    Sun, Ping
    Narod, Steven A.
    CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2006, 15 (09) : 1636 - 1640
  • [39] Prevalence of Alterations in DNA Mismatch Repair Genes in Patients With Young-Onset Colorectal Cancer
    Limburg, Paul J.
    Harmsen, William S.
    Chen, Helen H.
    Gallinger, Steven
    Haile, Robert W.
    Baron, John A.
    Casey, Graham
    Woods, Michael O.
    Thibodeau, Stephen N.
    Lindor, Noralane M.
    CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2011, 9 (06) : 497 - 502
  • [40] Prevalence and molecular characteristics of DNA mismatch repair deficient endometrial cancer in a Japanese hospital-based population
    Yamamoto, Azusa
    Yamaguchi, Tatsuro
    Suzuki, Okihide
    Ito, Tetsuya
    Chika, Noriyasu
    Kamae, Nao
    Tamaru, Jun-ichi
    Nagai, Tomonori
    Seki, Hiroyuki
    Arai, Tomio
    Tachikawa, Tetsuhiko
    Akagi, Kiwamu
    Eguchi, Hidetaka
    Okazaki, Yasushi
    Ishida, Hideyuki
    JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2021, 51 (01) : 60 - 69