Using Expression Profiling to Understand the Effects of Chronic Cadmium Exposure on MCF-7 Breast Cancer Cells

Zelmina Lubovac-Pilav, Daniel M. Borras, Esmeralda Ponce, Maggie C. Louie

Research output: Contribution to journalArticlepeer-review

Abstract

Cadmium is a metalloestrogen known to activate the estrogen receptor and promote breast cancer cell growth. Previous studies have implicated cadmium in the development of more malignant tumors; however the molecular mechanisms behind this cadmium-induced malignancy remain elusive. Using clonal cell lines derived from exposing breast cancer cells to cadmium for over 6 months (MCF-7-Cd4, -Cd6, -Cd7, -Cd8 and -Cd12), this study aims to identify gene expression signatures associated with chronic cadmium exposure. Our results demonstrate that prolonged cadmium exposure does not merely result in the deregulation of genes but actually leads to a distinctive expression profile. The genes deregulated in cadmium-exposed cells are involved in multiple biological processes (i.e. cell growth, apoptosis, etc.) and molecular functions (i.e. cadmium/metal ion binding, transcription factor activity, etc.). Hierarchical clustering demonstrates that the five clonal cadmium cell lines share a common gene expression signature of breast cancer associated genes, clearly differentiating control cells from cadmium exposed cells. The results presented in this study offer insights into the cellular and molecular impacts of cadmium on breast cancer and emphasize the importance of studying chronic cadmium exposure as one possible mechanism of promoting breast cancer progression.

Original languageAmerican English
Pages (from-to)e84646
JournalPLoS ONE
Volume8
Issue number12
StatePublished - Dec 20 2013

Funding

FundersFunder number
National Cancer InstituteCA121983-02, CA121983-02S1
National Cancer InstituteR15CA121983

    Keywords

    • cadmium
    • breast cancer
    • gene ontologies
    • gene expression
    • zinc
    • microarrays
    • cyclins
    • Cadmium/toxicity
    • Gene Expression Profiling/methods
    • Humans
    • MCF-7 Cells/drug effects
    • Gene Expression Regulation, Neoplastic/drug effects
    • DNA Primers/genetics
    • Reverse Transcriptase Polymerase Chain Reaction
    • Microarray Analysis
    • Female
    • Cluster Analysis

    Disciplines

    • Biochemistry
    • Oncology

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