Molecular pathology of pituitary adenomas

被引:21
作者
Lloyd, RV [1 ]
机构
[1] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN USA
关键词
pituitary; p27; p16; cyclin-dependent kinase inhibitors;
D O I
10.1023/A:1012940929072
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A great deal of knowledge about anterior pituitary development, the pathogenesis of pituitary tumor and pituitary tumor progression has accumulated during the past decade. The role of multiple genes and gene products in pituitary development and the relationship of these genes to postnatal pituitary function and pituitary tumor development are being actively explored. Recent studies indicate that genes important in pituitary development do not contribute to pituitary tumorigenesis. However, mutations and other genetic alterations in these genes often lead to pituitary hypofunction. Many oncogenes and tumor suppressor genes that contribute to pituitary tumorigenesis have been described. There is a growing body of evidence showing that cellular and molecular changes in cyclins and cyclin-dependent kinase inhibitors contribute to pituitary tumorigenesis. Finally, recent comparative genomic hybridization studies show that many more genes that are important in pituitary tumorigenesis and tumor progression have yet to bebreak discovered.
引用
收藏
页码:111 / 119
页数:9
相关论文
共 73 条
  • [1] Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states
    Agarwal, SK
    Kester, MB
    Debelenko, LV
    Heppner, C
    EmmertBuck, MR
    Skarulis, MC
    Doppman, JL
    Kim, YS
    Lubensky, IA
    Zhuang, ZP
    Green, JS
    Guru, SC
    Manickam, P
    Olufemi, SE
    Liotta, LA
    Chandrasekharappa, SC
    Collins, FS
    Spiegel, AM
    Burns, AL
    Marx, SJ
    [J]. HUMAN MOLECULAR GENETICS, 1997, 6 (07) : 1169 - 1175
  • [2] CLINICALLY NONFUNCTIONING PITUITARY-TUMORS ARE MONOCLONAL IN ORIGIN
    ALEXANDER, JM
    BILLER, BMK
    BIKKAL, H
    ZERVAS, NT
    ARNOLD, A
    KLIBANSKI, A
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (01) : 336 - 340
  • [3] The MEN-1 gene is rarely down-regulated in pituitary adenomas
    Asa, SL
    Somers, K
    Ezzat, S
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (09) : 3210 - 3212
  • [4] The cytogenesis and pathogenesis of pituitary adenomas
    Asa, SL
    Ezzat, S
    [J]. ENDOCRINE REVIEWS, 1998, 19 (06) : 798 - 827
  • [5] THE CYCLIC ADENOSINE 3',5'-MONOPHOSPHATE-RESPONSIVE FACTOR CREB IS CONSTITUTIVELY ACTIVATED IN HUMAN SOMATOTROPH ADENOMAS
    BERTHERAT, J
    CHANSON, P
    MONTMINY, M
    [J]. MOLECULAR ENDOCRINOLOGY, 1995, 9 (07) : 777 - 783
  • [6] Genealogy of the anterior pituitary gland: Tracing a family tree
    Burrows, HL
    Douglas, KR
    Seasholtz, AF
    Camper, SA
    [J]. TRENDS IN ENDOCRINOLOGY AND METABOLISM, 1999, 10 (09) : 343 - 352
  • [7] RAS MUTATIONS IN HUMAN PROLACTINOMAS AND PITUITARY CARCINOMAS
    CAI, WY
    ALEXANDER, JM
    HEDLEYWHYTE, ET
    SCHEITHAUER, BW
    JAMESON, JL
    ZERVAS, NT
    KLIBANSKI, A
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (01) : 89 - 93
  • [8] Prolactinomas in male and female patients: A comparative clinicopathologic study
    Calle-Rodrigue, RDP
    Giannini, C
    Scheithauer, BW
    Lloyd, RV
    Wollan, PC
    Kovacs, KT
    Stefaneanu, L
    Ebright, AB
    Abboud, CF
    Davis, DH
    [J]. MAYO CLINIC PROCEEDINGS, 1998, 73 (11) : 1046 - 1052
  • [9] SKP2 is required for ubiquitin-mediated degradation of the CDK inhibitor p27
    Carrano, AC
    Eytan, E
    Hershko, A
    Pagano, M
    [J]. NATURE CELL BIOLOGY, 1999, 1 (04) : 193 - 199
  • [10] Comparative genomic hybridization analysis of nonfunctioning pituitary tumors
    Daniely, M
    Aviram, A
    Adams, EF
    Buchfelder, M
    Barkai, G
    Fahlbusch, R
    Goldman, B
    Friedman, E
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (05) : 1801 - 1805