4.5 Review Book Chapter

Retinoids, Retinoic Acid Receptors, and Cancer

Journal

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev-pathol-011110-130303

Keywords

vitamin A; carcinogenesis; stem cells; differentiation; epigenetic changes; polycomb proteins

Categories

Funding

  1. NCI NIH HHS [R01 CA043796] Funding Source: Medline
  2. NIDCR NIH HHS [R01 DE010389] Funding Source: Medline
  3. NATIONAL CANCER INSTITUTE [R01CA043796] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH [R01DE010389] Funding Source: NIH RePORTER

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Retinoids (i.e., vitamin A, all-trans retinoic acid, and related signaling molecules) induce the differentiation of various types of stem cells. Nuclear retinoic acid receptors mediate most but not all of the effects of retinoids. Retinoid signaling is often compromised early in carcinogenesis, which suggests that a reduction in retinoid signaling may be required for tumor development. Retinoids interact with other signaling pathways, including estrogen signaling in breast cancer. Retinoids are used to treat cancer, in part because of their ability to induce differentiation and arrest proliferation. Delivery of retinoids to patients is challenging because of the rapid metabolism of some retinoids and because epigenetic changes can render cells retinoid resistant. Successful cancer therapy with retinoids is likely to require combination therapy with drugs that regulate the epigenome, such as DNA methyltransferase and histone deacetylase inhibitors, as well as classical chemotherapeutic agents. Thus, retinoid research benefits both cancer prevention and cancer treatment.

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