Microsatellite instability in gonadal tumors of XY pure gonadal dysgenesis patients

被引:3
作者
Funato, T
Uehara, S
Takahashi, M
Kozawa, K
Satoh, J
Sasaki, T
Kaku, M
机构
[1] Tohoku Univ, Sch Med, Dept Clin Med, Div Mol Diagnost,Aoba Ku, Sendai, Miyagi 9808574, Japan
[2] Tohoku Univ, Sch Med, Dept Clin Med, Div Rheumatol & Hematol, Sendai, Miyagi 9808574, Japan
[3] Tohoku Univ, Sch Med, Dept Obstet & Gynecol, Sendai, Miyagi 9808574, Japan
关键词
dysgerminoma; gonadoblastoma; microsatellite instability; ras mutation; XY pure gonadal dysgenesis;
D O I
10.1046/j.1525-1438.2002.01094.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To investigate genetic alternation accompanied by malignant transformation in gonadal tumors of XY pure gonadal dysgenesis patients, we investigated microsatellite instability in the hMSH1, hMSH2, TP53, and DCC loci, and ras mutations in two patients. The gonadal tumors from the patients were combined gonadoblastoma and dysgerminoma. Microsatellite instability and/or loss of heterozygotes (LOH) at hMSH1, hMSH2, and TP53 were detected in the dysgerminoma lesions of the both patients, but were not observed in any normal tissues. In the analyses of the H-, K-, or N-ras genes, where specific mutations have been frequently reported, no mutations were observed in the tumors. It is suggested therefore that microsatellite instability plays an important role in malignant transformation of gonadal tumors in patients with XY pure gonadal dysgenesis.
引用
收藏
页码:192 / 197
页数:6
相关论文
共 50 条
  • [1] Undifferentiated Gonadal Tissue, Y Chromosome Instability, and Tumors in XY Gonadal Dysgenesis
    Bergeron, Melanie Beaulieu
    Lemieux, Nicole
    Brochu, Pierre
    PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 2011, 14 (06) : 445 - 459
  • [2] Gonadoblastomas in 5 patients with 46,XY gonadal dysgenesis
    Hoepffner, W
    Horn, LC
    Simon, E
    Sauerbrei, G
    Schröder, H
    Thamm-Mücke, B
    Bennek, J
    Kiess, W
    EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 2005, 113 (04) : 231 - 235
  • [3] THE RISK FOR DEVELOPING TUMOR IN PATIENTS WITH GONADAL DYSGENESIS 46, XY
    Latyshev, O. Yu.
    Samsonova, L. N.
    Kasatkina, E. P.
    Okminyan, G. F.
    Kiselyova, Ye. V.
    Timofeyeva, Ye. S.
    BYULLETEN SIBIRSKOY MEDITSINY, 2015, 14 (05): : 41 - 46
  • [4] Swyer syndrome in a woman with pure 46,XY gonadal dysgenesis: a rare presentation
    Maharjan, A.
    Yao-dan, L.
    Li, H.
    CLINICAL AND EXPERIMENTAL OBSTETRICS & GYNECOLOGY, 2017, 44 (02) : 314 - 316
  • [5] 46,XY pure gonadal dysgenesis: Clinical presentations and management of the tumor risk
    Capito, Carmen
    Leclair, Marc-David
    Arnaud, Alexis
    David, Albert
    Baron, Sabine
    Corradini, Nadege
    Heloury, Yves
    JOURNAL OF PEDIATRIC UROLOGY, 2011, 7 (01) : 72 - 75
  • [6] Complete XY gonadal dysgenesis and aspects of the SRY genotype and gonadal tumor formation
    S. Uehara
    M. Hashiyada
    K. Sato
    M. Nata
    T. Funato
    K. Okamura
    Journal of Human Genetics, 2002, 47 : 279 - 284
  • [7] Ovarian Choriocarcinoma as the First Manifestation of 46,XY Pure Gonadal Dysgenesis
    Lee, Anselm Chi-wai
    Fong, Chee-meng
    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2011, 33 (01) : E29 - E31
  • [8] Dysgerminoma in a case of 46, XY pure gonadal dysgenesis (swyer syndrome): a case report
    Han, Yang
    Wang, Yan
    Li, Qingchang
    Dai, Shundong
    He, Anguang
    Wang, Enhua
    DIAGNOSTIC PATHOLOGY, 2011, 6
  • [9] An Unusual Presentation of 46,XY Pure Gonadal Dysgenesis: Spontaneous Breast Development and Menstruation
    Catli, Gonul
    Alparslan, Caner
    Can, P. Sule
    Akbay, Sinem
    Kelekci, Sefa
    Atik, Tahir
    Ozyilmaz, Berk
    Dundar, Bumin N.
    JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, 2015, 7 (02) : 159 - 162
  • [10] Familial Pure Gonadal Dysgenesis with 46, XY Karyotype in Three Siblings and Gonadoblastoma in the Youngest Sibling
    Eunice, M.
    Kulshreshtha, B.
    Kriplani, A.
    Dada, Rima
    Agarwal, S.
    Kucheria, K.
    Karak, A. K.
    Gupta, S. Datta
    Ammini, A. C.
    INTERNATIONAL JOURNAL OF HUMAN GENETICS, 2009, 9 (02) : 123 - 126