ANDROGEN RECEPTOR IN THE RAT PANCREAS - GENETIC EXPRESSION AND STEROID REGULATION

被引:27
作者
DIAZSANCHEZ, V
MORIMOTO, S
MORALES, A
ROBLESDIAZ, G
CERBON, M
机构
[1] INST NACL NUTR SALVADOR ZUBIRAN,DEPT GASTROENTEROL,MEXICO CITY 14000,DF,MEXICO
[2] NATL AUTONOMOUS UNIV MEXICO,FES ZARAGOZA,MOLEC BIOL UNIT REPROD HLTH,MEXICO CITY 04510,DF,MEXICO
关键词
ANDROGEN RECEPTOR; REVERSE TRANSCRIPTION; POLYMERASE CHAIN REACTION; RAT PANCREAS;
D O I
10.1097/00006676-199510000-00005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Androgens influence the incidence and prevalence of pancreatic cancer in humans and animal models. To our knowledge there has been molecular demonstration of the presence of neither the androgen receptor (AR) nor transcripts of the AR gene. Reverse-transcription polymerase chain reaction (RT-PCR)-Southern blotting was employed for molecular detection and measurement of the androgen receptor messenger ribonucleic acid (AR mRNA) in pancreas, Total RNA obtained from pancreas, prostate, seminal vesicles, and testes of neonatal and adult male and female rats, as well as castrated males substituted with testosterone cyclopentylate, was analyzed by Northern blot technique. Positive hybridization to AR cDNA was obtained in all tissues assayed but not in the pancreas, However, a clear AR P-32 cDNA hybridization signal was obtained in pancreatic tissues after cDNA synthesis using RT-PCR-Southern blotting, The levels of the AR transcripts obtained by RT-PCR in the various pancreatic samples were as follows: adult females and neonatal animals > castrated adult males > adult males > castrated adult males substituted with testosterone. These results indicated that the pancreatic tissue possessed transcriptional activity of the AR gene, although to a lesser extent than the typical androgen responsive tissues (prostate and seminal vesicles). In conclusion, transcriptional activity of the AR gene in the pancreas seemed to be modulated by the androgenic milieu in the tissue similar to that reported for the classical androgen-responsive organs.
引用
收藏
页码:241 / 245
页数:5
相关论文
共 19 条
[1]   GENE-REGULATION BY STEROID-HORMONES [J].
BEATO, M .
CELL, 1989, 56 (03) :335-344
[2]  
BENZ C, 1986, CANCER RES, V46, P2276
[3]   A METHOD FOR ISOLATION OF INTACT, TRANSLATIONALLY ACTIVE RIBONUCLEIC-ACID [J].
CATHALA, G ;
SAVOURET, JF ;
MENDEZ, B ;
WEST, BL ;
KARIN, M ;
MARTIAL, JA ;
BAXTER, JD .
DNA-A JOURNAL OF MOLECULAR & CELLULAR BIOLOGY, 1983, 2 (04) :329-335
[4]  
CROBISHLEY TP, 1986, CANCER, V57, P1992
[5]  
DEVOS P, 1983, MOL CELL ENDOCRINOL, V90, pR11
[6]  
FEIMBERG A, 1983, ANAL BIOCHEM, V137, P6
[7]  
FERNANDEZDELCAS.C, 1991, PANCREAS, V6, P104
[8]  
FERNANDEZDELCAS.C, 1990, PANCREAS, V5, P515
[9]   THE CONTROL OF HUMAN PANCREATIC ADENOCARCINOMA XENOGRAFTS IN NUDE-MICE BY HORMONE-THERAPY [J].
GREENWAY, B ;
DUKE, D ;
PYM, B ;
IQBAL, MJ ;
JOHNSON, PJ ;
WILLIAMS, R .
BRITISH JOURNAL OF SURGERY, 1982, 69 (10) :595-597
[10]   COMPLEMENTARY-DNA FOR HUMAN T-CELL CYCLOPHILIN [J].
HAENDLER, B ;
HOFERWARBINEK, R ;
HOFER, E .
EMBO JOURNAL, 1987, 6 (04) :947-950