Chronic Cadmium Exposure Stimulates SDF-1 Expression in an ERα Dependent Manner

Esmeralda Ponce, Natalie B. Aquino, Maggie Louie

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Cadmium is an omnipotent environmental contaminant associated with the development of breast cancer. Studies suggest that cadmium functions as an endocrine disruptor, mimicking the actions of estrogen in breast cancer cells and activating the receptor to promote cell growth. Although acute cadmium exposure is known to promote estrogen receptor-mediated gene expression associated with growth, the consequence of chronic cadmium exposure is unclear. Since heavy metals are known to bioaccumulate, it is necessary to understand the effects of prolonged cadmium exposure. This study aims to investigate the effects of chronic cadmium exposure on breast cancer progression. A MCF7 breast cancer cell line chronically exposed to 10−7 M CdCl2 serves as our model system. Data suggest that prolonged cadmium exposures result in the development of more aggressive cancer phenotypes – increased cell growth, migration and invasion. The results from this study show for the first time that chronic cadmium exposure stimulates the expression of SDF-1 by altering the molecular interactions between ERα, c-jun and c-fos. This study provides a mechanistic link between chronic cadmium exposure and ERα and demonstrates that prolonged, low-level cadmium exposure contributes to breast cancer progression

    Original languageAmerican English
    Article numbere72639
    Pages (from-to)e72639
    JournalPLoS ONE
    Volume8
    Issue number8
    DOIs
    StatePublished - Aug 28 2013

    Funding

    FundersFunder number
    National Cancer InstituteCA121983-02, CA121983-02S1, R15CA121983
    National Science Foundation1039728

      ASJC Scopus Subject Areas

      • General Biochemistry,Genetics and Molecular Biology
      • General Agricultural and Biological Sciences
      • General

      Keywords

      • cadmium
      • breast cancer
      • gene expression
      • small interferring RNAs
      • chromatin immunoprecipitation
      • transcription factors
      • estrogens

      Disciplines

      • Biochemistry
      • Oncology

      Cite this