Molecular defects in the pathogenesis of pituitary tumours

被引:61
作者
Levy, A [1 ]
Lightman, S [1 ]
机构
[1] Univ Bristol, Univ Res Ctr Neuroendocrinol, Bristol BS2 8HW, Avon, England
关键词
adenoma; clonality; aneuploidy; hypophysis; pituitary gland anterior; neuroendocrine; oncogenes;
D O I
10.1016/S0091-3022(03)00012-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The majority of pituitary adenomas are trophically stable and change relatively little in size over many years. A comparatively small proportion behave more aggressively and come to clinical attention through inappropriate hormone secretion or adverse effects on surrounding structures. True malignant behaviour with metastatic spread is very atypical. Pituitary adenomas that come to surgery are predominantly monoclonal in origin and roughly half are aneuploid, indicating either ongoing genetic instability or transition through a period of genetic instability at some time during their development. Few are associated with the classical mechanisms of tumour formation but it is generally believed that the majority harbour quantitative if not qualitative differences in molecular composition compared to the normal pituitary. Despite their prevalence and the ready availability of biopsy material, at the present time, the precise molecular pathogenesis of the majority of pituitary adenomas remains unclear. This review summarizes current thinking. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:94 / 127
页数:34
相关论文
共 542 条
[1]   CLUES TO THE PATHOGENESIS OF FAMILIAL COLORECTAL-CANCER [J].
AALTONEN, LA ;
PELTOMAKI, P ;
LEACH, FS ;
SISTONEN, P ;
PYLKKANEN, L ;
MECKLIN, JP ;
JARVINEN, H ;
POWELL, SM ;
JEN, J ;
HAMILTON, SR ;
PETERSEN, GM ;
KINZLER, KW ;
VOGELSTEIN, B ;
DELACHAPELLE, A .
SCIENCE, 1993, 260 (5109) :812-816
[2]   Altered expression of fibroblast growth factor receptors in human pituitary adenomas [J].
Abbass, SAA ;
Asa, SL ;
Ezzat, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (04) :1160-1166
[3]   Identification of a zinc-finger gene at 6q25: A chromosomal region implicated in development of many solid tumors [J].
Abdollahi, A ;
Roberts, D ;
Godwin, AK ;
Schultz, DC ;
Sonoda, G ;
Testa, JR ;
Hamilton, TC .
ONCOGENE, 1997, 14 (16) :1973-1979
[4]  
ABRAM M, 1992, ANN ENDOCRINOL-PARIS, V53, P215
[5]   MORPHOLOGICAL AND FUNCTIONAL POLYMORPHISM WITHIN CLONAL THYROID-NODULES [J].
AESCHIMANN, S ;
KOPP, PA ;
KIMURA, ET ;
ZBAEREN, J ;
TOBLER, A ;
FEY, MF ;
STUDER, H .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1993, 77 (03) :846-851
[6]   CLINICALLY NONFUNCTIONING PITUITARY-TUMORS ARE MONOCLONAL IN ORIGIN [J].
ALEXANDER, JM ;
BILLER, BMK ;
BIKKAL, H ;
ZERVAS, NT ;
ARNOLD, A ;
KLIBANSKI, A .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (01) :336-340
[8]  
ALEXANDROW MG, 1995, CANCER RES, V55, P1452
[9]   Cytology of Pituitary Thyrotroph Hyperplasia in Protracted Primary Hypothyroidism [J].
Ahmed M. Alkhani ;
Michael Cusimano ;
Kalman Kovacs ;
Juan M. Bilbao ;
Eva Horvath ;
William Singer .
Pituitary, 1999, 1 (3-4) :291-295
[10]   PROTEIN-KINASE-C ACTIVITY AND EXPRESSION IN NORMAL AND ADENOMATOUS HUMAN PITUITARIES [J].
ALVARO, V ;
TOURAINE, P ;
VOZARI, RR ;
BAIGRENIER, F ;
BIRMAN, P ;
JOUBERT, D .
INTERNATIONAL JOURNAL OF CANCER, 1992, 50 (05) :724-730