GSTM1 AND CYP2D6 GENOTYPE FREQUENCIES IN PATIENTS WITH PITUITARY-TUMORS - EFFECTS ON P53, RAS AND GSP

被引:15
作者
PERRETT, CW
CLAYTON, RN
PISTORELLO, M
BOSCARO, M
SCANARINI, M
BATES, AS
BUCKLEY, N
JONES, P
FRYER, AA
GILFORD, J
ALLDERSEA, J
STRANGE, RC
机构
[1] KEELE UNIV,N STAFFORDSHIRE HOSP,POSTGRAD MED SCH,CTR PATHOL & MOLEC MED,STOKE ON TRENT ST4 7QB,STAFFS,ENGLAND
[2] UNIV PADUA,IST SEMEIOT MED,I-35100 PADUA,ITALY
关键词
D O I
10.1093/carcin/16.7.1643
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We describe studies to determine if susceptibility to pituitary tumours is associated with the putatively high risk GSTM1 null and CYP2D6 EM genotypes. Frequency distributions of these genotypes were similar in cases and controls though the frequency of CYP2D6 PM and GSTM1 B tended to be lower (P = 0.072 and P = 0.095 respectively) in the tumour group. Immunopositivity for p53 was found in 18/97 tumours. In these samples GSTM1 null (39%) and CYP2D6 EM (56%) frequencies were not different to those in controls. The frequencies of CYP2D6 PM and GSTM1 B in the p53 immunonegative tumours tended to be lower (P = 0.055 and P = 0.1185 respectively) than in controls. Mutations in gsp and ras were studied using the polymerase chain reaction and allele specific oligonucleotide analysis. Eight of 19 somatotrophinomas demonstrated mutations in gsp; frequencies of GSTM1 null and CYP2D6 EM were similar to controls. No ras mutations were identified in 55-tumour studies. The data indicate the GSTM1 null and CYP2D6 EM genotypes are not associated with altered expression of p53 or, mutation of gsp and ras in these adenomas and, suggest the CYP2D6 PM genotype is associated with a reduced risk of pituitary adenomas and, that GSTM1*B confers greater protection than GSTM1*A.
引用
收藏
页码:1643 / 1645
页数:3
相关论文
共 17 条
[1]   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
[2]  
BROCKMOLLER J, 1994, CANCER RES, V54, P4103
[3]   P53 PROTEIN ACCUMULATES IN CUSHINGS ADENOMAS AND INVASIVE NONFUNCTIONAL ADENOMAS [J].
BUCKLEY, N ;
BATES, AS ;
BROOME, JC ;
STRANGE, RC ;
PERRETT, CW ;
BURKE, CW ;
CLAYTON, RN .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 79 (05) :1513-1516
[4]   THE GLUTATHIONE S-TRANSFERASES - POLYMERASE CHAIN-REACTION STUDIES ON THE FREQUENCY OF THE GSTM1 0 GENOTYPE IN PATIENTS WITH PITUITARY-ADENOMAS [J].
FRYER, AA ;
ZHAO, L ;
ALLDERSEA, J ;
BOGGILD, MD ;
PERRETT, CW ;
CLAYTON, RN ;
JONES, PW ;
STRANGE, RC .
CARCINOGENESIS, 1993, 14 (04) :563-566
[5]   GLUTATHIONE-S-TRANSFERASE GSTM1 PHENOTYPES AND PROTECTION AGAINST CUTANEOUS TUMORS [J].
HEAGERTY, AHM ;
FITZGERALD, D ;
SMITH, A ;
BOWERS, B ;
JONES, P ;
FRYER, AA ;
ZHAO, L ;
ALLDERSEA, J ;
STRANGE, RC .
LANCET, 1994, 343 (8892) :266-268
[6]   PCR-BASED CYP2D6 GENOTYPING FOR FINNISH LUNG-CANCER PATIENTS [J].
HIRVONEN, A ;
HUSGAFVELPURSIAINEN, K ;
ANTTILA, S ;
KARJALAINEN, A ;
PELKONEN, O ;
VAINIO, H .
PHARMACOGENETICS, 1993, 3 (01) :19-27
[7]   RAS MUTATIONS IN HUMAN PITUITARY-TUMORS [J].
KARGA, HJ ;
ALEXANDER, JM ;
HEDLEYWHYTE, ET ;
KLIBANSKI, A ;
JAMESON, JL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1992, 74 (04) :914-919
[8]  
KETTERER B, 1993, STRUCTURE FUNCTION G, P15
[9]  
NAZARSTEWART V, 1993, CANCER RES, V53, P2313
[10]  
ROOTS I, 1992, CLIN PHARMACOL THER, V51, P181