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Mouse mammary tumor virus-like gene sequences in breast cancer samples of Mexican women

  • P. Zapata-Benavides
    ,
  • ,
  • D. Zamora-Avila
    ,
  • C. Vargas-Rodarte
    ,
  • R. Barrera-Rodríguez
    ,
  • J. Salinas-Silva
*Corresponding author for this work
  • Universidad Autonoma de Nuevo Leon
    ,
  • Instituto Nacional de Enfermedades Respiratorias
    ,
  • Laboratorio de Anatomía Patológica
Research Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Publication metrics

Metrics

SciVal
FWCI
0.52
SciVal
Author count
9
SciVal
Paper percentile
58
SciVal
Citations
33
Scopus
Citations

Abstract

Background: Previous reports related the presence of mouse mammary tumor virus (MMTV)-like gene sequences to human breast carcinoma. The aim of this study was to determine whether MMTV-like env gene sequences are present in breast cancer samples of Mexican women and in breast and lung cancer cell lines. Methods: Using specific primers for MMTV, we tested 3 breast cancer cell lines, 4 non-small lung cancer cell lines and 119 breast cancer samples from Mexican women. Results: MMTV-like gene sequences were amplified in the lung cancer cell INER-51, but not in the MCF-7 cell line that has been used as a positive control in other reports and in 5 of 119 (4.2%) breast cancer biopsy tissues. Furthermore, the identity of sequences of PCR products from INER-51 and a breast cancer-positive sample are 98 and 99% when compared with the env region of MMTV (GenBank accession No. AY161347). Conclusion: These results indicate that MMTV-like gene sequences are present in the Mexican population.

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 402-407 (6 pages)

Journal (Volume, Issue Number)

Intervirology (Volume 50, Issue 6)

Publication milestones

  • Published - 02/2008

Publication status

Published - 02/2008

ISSN

0300-5526

Publication IDs

  • ORCID: /0000-0001-9495-7994/work/34115365
  • Scopus: 39749098426
  • PubMed: 17975321