Sequences Homologous to the Mouse Mammary Tumor Virus env Gene in Human Breast Carcinoma Correlate with Overexpression of Laminin Receptor

We previously reported that a 660-bp sequence that is homologous to the env gene of the mouse mammary tumor virus (MMTV) but not to endogenous retroviruses or to other known genes was present in 38% of human breast cancers and in some breast cancer cell lines studied (Y. Wang et al. , Cancer Res., 5...

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Veröffentlicht in:Clinical cancer research 1999-08, Vol.5 (8), p.2108-2111
Hauptverfasser: POGO, B. G.-T, MELANA, S. M, HOLLAND, J. F, MANDELI, J. F, PILOTTI, S, CASALINI, P, MENARD, S
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Sprache:eng
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Zusammenfassung:We previously reported that a 660-bp sequence that is homologous to the env gene of the mouse mammary tumor virus (MMTV) but not to endogenous retroviruses or to other known genes was present in 38% of human breast cancers and in some breast cancer cell lines studied (Y. Wang et al. , Cancer Res., 55: 5173–5179, 1995). Here, we have investigated whether the MMTV-like sequences were associated with the clinical, pathological, and molecular parameters that have been reported to define two subsets of human breast cancers. Archival breast carcinoma samples were analyzed for four clinical parameters, obtained from patients’ records, and for six pathological characteristics. Expression of c-erbB-2, p53, bcl-2, progesterone receptor, laminin receptor, and cathepsin D was detected by immunochemistry using monoclonal antibodies. PCRs were used to amplify 250 bp of the MMTV env gene-like sequence. The χ 2 , log-rank, and generalized Wilcoxon tests were used to analyze the data. The MMTV env gene-like sequence was detected in 37.7% of the samples. The presence of this sequence was not significantly associated with any of the pathological clinical or biological parameters studied. It did correlate, however, with expression of the laminin receptor, a marker for invasiveness and poor prognosis. This is the first phenotypic characterization of human breast cancers containing retroviral sequences.
ISSN:1078-0432
1557-3265