Key result
Estradiol increases CAR levels and adenoviral transduction in ER-positive breast cancer cells, driving estrogen-dependent proliferation.
Why the study?
The involvement of the coxsackie and adenovirus receptor (CAR) in breast cancer and its regulation by estrogen was under investigation to understand its role in cancer proliferation and gene therapy delivery.
The coxsackie and adenovirus receptor (CAR) is an estrogen-responsive gene that mediates estrogen-dependent proliferation in breast cancer cells.
Answers are grounded in this paper and cite their sources.
CAR modulation merits preclinical exploration in ER+ breast cancer; leaves open its role in estrogen signaling and adenoviral therapy.
The involvement of the coxsackie and adenovirus receptor (CAR), an adhesion molecule known to be the main determinant of adenovirus transduction of the cells, in cancer is currently under investigation. Recent reports suggest that CAR levels are elevated in breast cancer, and this may have an impact on its use as means of delivery for gene therapy. In this study, we show that estradiol (E(2)) treatment of the estrogen receptor (ER)-positive breast cancer cell MCF-7 increases CAR levels and, in turn, enhances adenoviral transduction. Employing the transfection of CAR promoters in breast cancer cells, we show that this regulation of CAR expression occurs at the transcriptional level. In addition, and by chromatin immunoprecipitation, we have identified a crucial region of CAR promoter that controls E(2) responsiveness of CAR gene through the recruitment of ER. Moreover, utilizing CAR antibodies or CAR silencing by RNA interference repressed the estrogen-dependent growth of breast cancer cells, whereas the stable expression of CAR in MCF-7 or MDA-MB-231 cells led to an increased proliferation. Altogether, our data suggest that CAR is a novel estrogen-responsive gene, which is involved in the E(2)-dependent proliferation of breast cancer cells.
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Vindrieux et al. (2011) studied Breast cancer. Estradiol (E2) treatment was evaluated on CAR expression, adenoviral transduction, and cell proliferation. Estradiol treatment increased CAR levels and adenoviral transduction in ER-positive breast cancer cells, while CAR expression promoted estrogen-dependent cell proliferation.
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