Possibilities of a viral etiology for human breast cancer - A review

被引:52
作者
Pogo, BGT
Holland, JF
机构
[1] CUNY MT SINAI SCH MED, DEPT MED, NEW YORK, NY 10029 USA
[2] CUNY MT SINAI SCH MED, DEPT MICROBIOL, NEW YORK, NY 10029 USA
关键词
breast cancer; retroviral sequences;
D O I
10.1007/BF02778989
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previous studies related mouse mammary tumor virus (MMTV) to human breast cancer. However, the presence of human endogenous retroviruses (HERs) confounded these results. We selected a 660-bp sequence of the MMTV env gene with low homology to HER (or any other known gene) and searched for a sequence homologous to it, using the polymerase chain reaction (PCR). The 660-bp sequence was detected in 131 (39%) of 335 unselected breast cancers, in 2 (6.9%) of 29 fibroadenomas, and in 2 (1.65%) of 121 normal breast specimens. The sequence was not present in normal tissues, or in other human cancers or cell, lines. Cloning and sequencing of the 660-bp sequence revealed that it is 95-98% homologous to MMTV env gene, but not the known HERs or other viral or human gene. Southern blot hybridization using labeled cloned sequences demonstrated that the 660-bp sequence was present in very low copy number as a 6-8 kb EcoRI fragment only in breast cancer samples and in some of the human breast cancer cell lines that were positive by PCR. Preliminary experiments using reverse transcriptase (RT)-PCR indicated that expression of the 660-bp sequence can be detected in 65% of the positive tumors. We were also able to identify in breast cancer DNA a segment of 1.6 kb comprising LTR and env gene sequences, which are homologous to MMTV, but not to the HERs. The origin of the MMTV-like sequences in tumor DNA could be the result of integrated MMTV-like sequences derived from a human mammary virus.
引用
收藏
页码:131 / 142
页数:12
相关论文
共 84 条
[61]   INHIBITION OF GENESIS OF SPONTANEOUS MAMMARY-TUMORS IN C3H MICE - EFFECTS OF SELENIUM AND OF SELENIUM-ANTAGONISTIC ELEMENTS AND THEIR POSSIBLE ROLE IN HUMAN BREAST-CANCER [J].
SCHRAUZER, GN ;
WHITE, DA ;
SCHNEIDER, CJ .
BIOINORGANIC CHEMISTRY, 1976, 6 (03) :265-270
[62]  
SCHRAUZER GN, 1974, ANN CLIN LAB SCI, V4, P441
[63]  
SCHUURING E, 1992, CANCER RES, V52, P5229
[64]  
SCHWARTZ MA, 1993, CANCER RES, V53, P1503
[65]  
SEGALEIRAS A, 1983, ARCH GESCHWULSTFORSC, V53, P321
[66]   MOUSE MAMMARY-TUMOR VIRUS-INFECTION ACCELERATES MAMMARY CARCINOGENESIS IN WNT-1 TRANSGENIC MICE BY INSERTIONAL ACTIVATION OF INT-2/FGF-3 AND HST/FGF-4 [J].
SHACKLEFORD, GM ;
MACARTHUR, CA ;
KWAN, HC ;
VARMUS, HE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (02) :740-744
[67]  
SIMON M, 1994, LEUKEMIA, V8, pS12
[68]   STUDIES OF THE HER-2/NEU PROTO-ONCOGENE IN HUMAN-BREAST AND OVARIAN-CANCER [J].
SLAMON, DJ ;
GODOLPHIN, W ;
JONES, LA ;
HOLT, JA ;
WONG, SG ;
KEITH, DE ;
LEVIN, WJ ;
STUART, SG ;
UDOVE, J ;
ULLRICH, A ;
PRESS, MF .
SCIENCE, 1989, 244 (4905) :707-712
[69]   HUMAN-BREAST CANCER - CORRELATION OF RELAPSE AND SURVIVAL WITH AMPLIFICATION OF THE HER-2 NEU ONCOGENE [J].
SLAMON, DJ ;
CLARK, GM ;
WONG, SG ;
LEVIN, WJ ;
ULLRICH, A ;
MCGUIRE, WL .
SCIENCE, 1987, 235 (4785) :177-182
[70]   INCIDENCE OF DE-NOVO BREAST-CANCER IN WOMEN CHRONICALLY IMMUNOSUPPRESSED AFTER ORGAN-TRANSPLANTATION [J].
STEWART, T ;
TSAI, SJ ;
GRAYSON, H ;
HENDERSON, R ;
OPELZ, G .
LANCET, 1995, 346 (8978) :796-798