EXPRESSION AND AMPLIFICATION OF THE HER-2/NEU (C-ERB-2) PROTOONCOGENE IN EPITHELIAL OVARIAN-TUMORS AND CELL-LINES

被引:70
作者
TYSON, FL
BOYER, CM
KAUFMAN, R
OBRIANT, K
CRAM, G
CREWS, JR
SOPER, JT
DALY, L
FOWLER, WC
HASKILL, JS
BAST, RC
机构
[1] DUKE UNIV,MED CTR,DEPT MED,BOX 3843,DURHAM,NC 27710
[2] DUKE UNIV,MED CTR,DEPT MICROBIOL IMMUNOL,DURHAM,NC 27710
[3] DUKE UNIV,MED CTR,DEPT OBSTET & GYNECOL,DURHAM,NC 27710
[4] DUKE UNIV,MED CTR,DUKE COMPREHENS CANC CTR,DURHAM,NC 27710
[5] UNIV N CAROLINA,DEPT OBSTET & GYNECOL,CHAPEL HILL,NC 27514
关键词
PROTOONCOGENES IN OVARIAN CANCER; C-ERB B-2; HER-2; NEU;
D O I
10.1016/0002-9378(91)90300-G
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Amplification of the c-erbB-2 protooncogene has been associated with a poor prognosis in human breast and ovarian cancers. Our study was undertaken to examine whether amplification, rearrangement, or overexpression of c-erbB-2 and other protooncogenes was frequently observed in epithelial ovarian cancers. c-erbB-2 was expressed in 87% of 22 ovarian cancers analyzed, but expression was significantly increased in only one of the 22 tumor specimens. In this case elevated c-erbB-2 expression was associated with dramatic amplification of the gene. In another tumor a 3.8 kb EcoRI fragment was found, in addition to the usual 4.4 and 6.0 kb fragments; this is consistent with a possible gene rearrangement or a restriction fragment length polymorphism. To place these results in perspective, expression of several other protooncogenes has been examined in ovarian carcinomas. The c-fos, c-myc, n-myc, c-fms, and c-Ha-ras protooncogenes were expressed in different fractions of tumors, but expression of l-myc, c-erbB, c-myb, c-sis, and c-mos was not detectable. Aside from c-erbB-2, neither amplification nor rearrangement was observed among the other protooncogenes studied. Expression of c-erbB-2, c-fms, c-myc, n-myc, c-fos, and c-Ha-ras deserves further evaluation as a prognostic factor in ovarian cancer.
引用
收藏
页码:640 / 646
页数:7
相关论文
共 21 条
  • [1] BERCHUCK A, 1990, CANCER RES, V50, P4087
  • [2] AMPLIFICATION OF C-RAS-KI ONCOGENE IN HUMAN OVARIAN-TUMORS
    BOLTZ, EM
    KEFFORD, RF
    LEARY, JA
    HOUGHTON, CR
    FRIEDLANDER, ML
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1989, 43 (03) : 428 - 430
  • [3] FASANO O, 1983, Journal of Molecular and Applied Genetics, V2, P173
  • [4] GREINER JW, 1984, CANCER RES, V44, P3208
  • [5] ISOLATION AND CHARACTERIZATION OF FULL-LENGTH CDNA CLONES FOR HUMAN ALPHA-ACTIN, BETA-ACTIN AND GAMMA-ACTIN MESSENGER-RNAS - SKELETAL BUT NOT CYTOPLASMIC ACTINS HAVE AN AMINO-TERMINAL CYSTEINE THAT IS SUBSEQUENTLY REMOVED
    GUNNING, P
    PONTE, P
    OKAYAMA, H
    ENGEL, J
    BLAU, H
    KEDES, L
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1983, 3 (05) : 787 - 795
  • [6] KACINSKI BM, 1989, YALE J BIOL MED, V62, P379
  • [7] TRANSPOSITION AND AMPLIFICATION OF ONCOGENE-RELATED SEQUENCES IN HUMAN NEUROBLASTOMAS
    KOHL, NE
    KANDA, N
    SCHRECK, RR
    BRUNS, G
    LATT, SA
    GILBERT, F
    ALT, FW
    [J]. CELL, 1983, 35 (02) : 359 - 367
  • [8] OVEREXPRESSION OF THE EGF RECEPTOR-RELATED PROTOONCOGENE ERBB-2 IN HUMAN MAMMARY-TUMOR CELL-LINES BY DIFFERENT MOLECULAR MECHANISMS
    KRAUS, MH
    POPESCU, NC
    AMSBAUGH, SC
    KING, CR
    [J]. EMBO JOURNAL, 1987, 6 (03) : 605 - 610
  • [9] MASUDA H, 1987, MOL BIOL MED, V4, P213
  • [10] MCCACHREN SS, 1986, BLOOD, V68, P412