MTAP gene deletion in endometrial cancer

被引:23
作者
Wong, YF [1 ]
Chung, TKH
Cheung, TH
Nobori, T
Chang, AMZ
机构
[1] Chinese Univ Hong Kong, Dept Obstet & Gynecol, Shatin, NT, Hong Kong
[2] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
关键词
deletion; endometrial cancer; MTAP;
D O I
10.1159/000009983
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
A gene (MTAP) that encodes the enzyme 5'-deoxy-5'-methylthioadenosine (MTA) phosphorylase has been identified on chromosome 9p21 and cloned. The substrate of this enzyme, MTA, inhibits aminopropyltransferases that synthesize polyamines from putrescine and decarboxylated S-adenosylmethionine. This enzyme normally cleaves MTA to adenine and 5'-methylthioribose-1-phosphate, which are recycled to adenine nucleotides and methionine, respectively. Cancers with deletions of the MTAP gene may be especially susceptible to chemotherapeutic regimes which interfere with purine or methionine utilization. The purpose of this study was to determine deletion of the MTAP gene in endometrial cancer using a polymerase chain reaction-based method. Therefore, 50 endometrial adenocarcinomas were studied. Partial or total deletions of the MTAP gene were detected in 7 (14%) of these cancers. There were no significant relationships between gene deletion and patient age, pathological grade or clinical stage (p > 0.05). The findings indicate that deletion of the MTAP gene does occur in a subgroup of endometrial cancer. The present work may be extended to the development of molecular diagnosis of MTAP gene deletion in other cancers and assist in selecting appropriate chemotherapy.
引用
收藏
页码:272 / 276
页数:5
相关论文
共 14 条
[1]  
Chen ZH, 1996, CANCER RES, V56, P1083
[2]   DEFICIENCY OF 5'-DEOXY-5'-METHYLTHIOADENOSINE PHOSPHORYLASE-ACTIVITY IN MALIGNANCY - ABSENCE OF THE PROTEIN IN HUMAN ENZYME-DEFICIENT CELL-LINES [J].
DELLARAGIONE, F ;
OLIVA, A ;
PALUMBO, R ;
RUSSO, GL ;
GRAGNANIELLO, V ;
ZAPPIA, V .
BIOCHEMICAL JOURNAL, 1992, 281 :533-538
[3]  
Hori H, 1996, CANCER RES, V56, P5653
[4]   Chromosome 9 related aberrations and deletions of the CDKN2 and MTS2 putative tumor suppressor genes in human chondrosarcomas [J].
Jagasia, AA ;
Block, JA ;
Qureshi, A ;
Diaz, MO ;
Nobori, T ;
Gitelis, S ;
Iyer, AP .
CANCER LETTERS, 1996, 105 (01) :91-103
[5]  
NOBORI T, 1991, CANCER RES, V51, P3193
[6]   Genomic cloning of methylthioadenosine phosphorylase: A purine metabolic enzyme deficient in multiple different cancers [J].
Nobori, T ;
Takabayashi, K ;
Tran, P ;
Orvis, L ;
Batova, A ;
Yu, AL ;
Carson, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (12) :6203-6208
[7]  
NOBORI T, 1993, CANCER RES, V53, P1098
[8]  
Sambrook J., 2002, MOL CLONING LAB MANU
[9]   5'-DEOXY-5'-METHYLTHIOADENOSINE PHOSPHORYLASE .2. ROLE OF THE ENZYME IN THE METABOLISM AND ANTI-NEOPLASTIC ACTION OF ADENINE-SUBSTITUTED ANALOGS OF 5'-DEOXY-5'-METHYLTHIOADENOSINE [J].
SAVARESE, TM ;
DEXTER, DL ;
PARKS, RE ;
MONTGOMERY, JA .
BIOCHEMICAL PHARMACOLOGY, 1983, 32 (12) :1907-1916
[10]  
STADLER WM, 1994, CANCER RES, V54, P2060