PURINE-BINDING FACTOR (NM23) GENE-EXPRESSION IN PITUITARY-TUMORS - MARKER OF ADENOMA INVASIVENESS

被引:51
作者
TAKINO, H
HERMAN, V
WEISS, M
MELMED, S
机构
[1] UNIV CALIF LOS ANGELES, SCH MED, CEDARS SINAI RES INST, DEPT MED, LOS ANGELES, CA 90048 USA
[2] UNIV SO CALIF, SCH MED, DEPT NEUROSURG, LOS ANGELES, CA 90048 USA
关键词
D O I
10.1210/jc.80.5.1733
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To determine the molecular distinction between invasive and noninvasive pituitary adenomas, we evaluated expression of the metastasizing suppressor gene, nm23, in tumors of varying stages. The nm23 gene was recently identified on the basis of reduced expression in highly metastic cancer compared with its expression in low metastatic potential tumors. Twenty-two pituitary tumors (10 nonfunctioning, 9 acromegaly, 2 prolactinomas, and 1 Cushing) were studied. H1 and H2 isoform expression of nm23 was investigated using a ribonuclease protection assay. nm23 H2 messenger ribonucleic acid expression was significantly reduced in invasive tumors and correlated highly (P = 0.0016) with cavernous sinus invasion. In these invasive tumors, sequencing of the nm23 gene did not reveal a mutation. Invasive tumors also demonstrated markedly reduced immunostaining for nm23 H2. These results show the relevance of nm23 gene expression to behavior of these benign tumors. High expression of nm23 H2 is associated with noninvasive pituitary adenomas and may restrain tumor aggression. This molecular defect distinguishing invasive from noninvasive tumors is shown to be a sensitive marker of adenoma invasiveness and may be a predictor for postoperative management plans.
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页码:1733 / 1738
页数:6
相关论文
共 33 条
[1]  
BEVILACQUA G, 1989, CANCER RES, V49, P5185
[2]   A DROSOPHILA GENE THAT IS HOMOLOGOUS TO A MAMMALIAN GENE ASSOCIATED WITH TUMOR-METASTASIS CODES FOR A NUCLEOSIDE DIPHOSPHATE KINASE [J].
BIGGS, J ;
HERSPERGER, E ;
STEEG, PS ;
LIOTTA, LA ;
SHEARN, A .
CELL, 1990, 63 (05) :933-940
[3]   MOLECULAR-GENETIC STUDIES OF SPORADIC PITUITARY-TUMORS [J].
BOGGILD, MD ;
JENKINSON, S ;
PISTORELLO, M ;
BOSCARO, M ;
SCANARINI, M ;
MCTERNAN, P ;
PERRETT, CW ;
THAKKER, RV ;
CLAYTON, RN .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (02) :387-392
[4]   RAS MUTATIONS IN HUMAN PROLACTINOMAS AND PITUITARY CARCINOMAS [J].
CAI, WY ;
ALEXANDER, JM ;
HEDLEYWHYTE, ET ;
SCHEITHAUER, BW ;
JAMESON, JL ;
ZERVAS, NT ;
KLIBANSKI, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (01) :89-93
[5]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[6]   SURGICAL-MANAGEMENT OF ACROMEGALY [J].
FAHLBUSCH, R ;
HONEGGER, J ;
BUCHFELDER, M .
ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 1992, 21 (03) :669-692
[7]  
FROHMAN LA, 1987, ENDOCRINOL METAB, P247
[8]  
GILLES AM, 1991, J BIOL CHEM, V266, P8784
[9]   HETEROGENEOUS EXPRESSION OF 2 SOMATOSTATIN RECEPTOR SUBTYPES IN PITUITARY-TUMORS [J].
GREENMAN, Y ;
MELMED, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (02) :398-403
[10]  
HERMAN V, 1993, J CLIN ENDOCR METAB, V77, P50, DOI 10.1210/jcem.77.1.8100831