Molecular alterations in early gastric carcinomas -: No apparent correlation with Helicobacter pylori status

被引:0
作者
Blok, P
Craanen, ME
Offerhaus, GJ
Dekker, W
Kuipers, EJ
Meuwissen, SG
Tytgat, GN
机构
[1] Westeinde Ziekenhuis, Dept Pathol, NL-2501 CK The Hague, Netherlands
[2] Vrije Univ Amsterdam Hosp, Dept Gastroenterol, Amsterdam, Netherlands
[3] Acad Med Ctr, Dept Gastroenterol, Amsterdam, Netherlands
[4] Acad Med Ctr, Dept Pathol, Amsterdam, Netherlands
[5] Kennemer Gasthuis Haarlewm, Dept Internal Med, Haarlem, Netherlands
关键词
early gastric carcinoma; Helicobacter pylori; gastric carcinogenesis; oncogenes; p53 tumor suppressor gene; E-cadherin gene;
D O I
暂无
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Data on the differences in molecular profile between H pylori-positive and H pylori-negative early gastric carcinomas, if any, are almost nonexistent. We therefore investigated whether molecular differences can be observed between H pylori-positive and H pylori-negative early gastric carcinomas. Forty-five early gastric carcinomas were analyzed for alterations in certain oncogenes (ras, MDM2, c-erbB-2, cyclin D1), the p53 tumor suppressor gene, and the e-cadherin gene. Of these 28 carcinomas were H pylori-positive, and 17 were H pylori-negative. No significant differences were found in the groups irrespective of Lauren type; ras (0% vs 0%), MDM2 (0% vs 0%), c-erbB-2 (0% vs 0%), cyclin D1 (18% vs 29%), p53 (68% vs 47%), and e-cadherin (46% vs 41%). Helicobacter pylori-positive and H pylori-negative early gastric carcinomas do not differ in molecular profile. Although they may prove different when tested for other abnormalities, our findings suggest that the acquisition of molecular alterations occurs via an H pylori independent pathway.
引用
收藏
页码:241 / 247
页数:7
相关论文
共 39 条
[21]   P53 EXPRESSION AND PROGNOSIS IN GASTRIC-CARCINOMA [J].
MARTIN, HM ;
FILIPE, MI ;
MORRIS, RW ;
LANE, DP ;
SILVESTRE, F .
INTERNATIONAL JOURNAL OF CANCER, 1992, 50 (06) :859-862
[22]   MDM2 EXPRESSION IN LYMPHOID-CELLS AND REACTIVE AND NEOPLASTIC LYMPHOID-TISSUE - COMPARATIVE-STUDY WITH P53 EXPRESSION [J].
MARTINEZ, JC ;
MATEO, M ;
SANCHEZBEATO, M ;
VILLUENDAS, R ;
ORRADRE, JL ;
ALGARA, P ;
SANCHEZVERDE, L ;
GARCIA, P ;
LOPEZ, C ;
MARTINEZ, P ;
PIRIS, MA .
JOURNAL OF PATHOLOGY, 1995, 177 (01) :27-34
[23]   MDM2 AND P53 - A QUESTION OF BALANCE [J].
MELTZER, PS .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (17) :1265-1266
[24]   THE MDM-2 ONCOGENE PRODUCT FORMS A COMPLEX WITH THE P53 PROTEIN AND INHIBITS P53-MEDIATED TRANSACTIVATION [J].
MOMAND, J ;
ZAMBETTI, GP ;
OLSON, DC ;
GEORGE, D ;
LEVINE, AJ .
CELL, 1992, 69 (07) :1237-1245
[25]   HISTOLOGIC TYPES OF GASTRIC CARCINOMA IN HIGH- AND LOW-RISK AREAS [J].
MUNOZ, N ;
CORREA, P ;
CUELLO, C ;
DUQUE, E .
INTERNATIONAL JOURNAL OF CANCER, 1968, 3 (06) :809-&
[26]  
MURAKAMI T, 1971, EARLY GASTRIC CANC, V11, P53
[27]   HELICOBACTER-PYLORI INFECTION AND GASTRIC-CARCINOMA AMONG JAPANESE-AMERICANS IN HAWAII [J].
NOMURA, A ;
STEMMERMANN, GN ;
CHYOU, PH ;
KATO, I ;
PEREZPEREZ, GI ;
BLASER, MJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (16) :1132-1136
[28]   ONCOPROTEIN MDM2 CONCEALS THE ACTIVATION DOMAIN OF TUMOR SUPPRESSOR-P53 [J].
OLINER, JD ;
PIETENPOL, JA ;
THIAGALINGAM, S ;
GVURIS, J ;
KINZLER, KW ;
VOGELSTEIN, B .
NATURE, 1993, 362 (6423) :857-860
[29]   HELICOBACTER-PYLORI INFECTION AND THE RISK OF GASTRIC-CARCINOMA [J].
PARSONNET, J ;
FRIEDMAN, GD ;
VANDERSTEEN, DP ;
CHANG, Y ;
VOGELMAN, JH ;
ORENTREICH, N ;
SIBLEY, RK .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (16) :1127-1131
[30]  
PRESS MF, 1994, CANCER RES, V54, P2771