9-Cis-Retinoic Acid Induces Growth Inhibition in Retinoid-Sensitive Breast Cancer and Sea Urchin Embryonic Cells via Retinoid X Receptor α and Replication Factor …

S Maeng, GJ Kim, EJ Choi, HO Yang… - Molecular …, 2012 - academic.oup.com
S Maeng, GJ Kim, EJ Choi, HO Yang, DS Lee, YC Sohn
Molecular Endocrinology, 2012academic.oup.com
There is widespread interest in defining factors and mechanisms that suppress the
proliferation of cancer cells. Retinoic acid (RA) is a potent suppressor of mammary cancer
and developmental embryonic cell proliferation. However, the molecular mechanisms by
which 9-cis-RA signaling induces growth inhibition in RA-sensitive breast cancer and
embryonic cells are not apparent. Here, we provide evidence that the inhibitory effect of 9-cis-
RA on cell proliferation depends on 9-cis-RA-dependent interaction of retinoid X receptor α …
Abstract
There is widespread interest in defining factors and mechanisms that suppress the proliferation of cancer cells. Retinoic acid (RA) is a potent suppressor of mammary cancer and developmental embryonic cell proliferation. However, the molecular mechanisms by which 9-cis-RA signaling induces growth inhibition in RA-sensitive breast cancer and embryonic cells are not apparent. Here, we provide evidence that the inhibitory effect of 9-cis-RA on cell proliferation depends on 9-cis-RA-dependent interaction of retinoid X receptor α (RXRα) with replication factor C3 (RFC3), which is a subunit of the RFC heteropentamer that opens and closes the circular proliferating cell nuclear antigen (PCNA) clamp on DNA. An RFC3 ortholog in a sea urchin cDNA library was isolated by using the ligand-binding domain of RXRα as bait in a yeast two-hybrid screening. The interaction of RFC3 with RXRα depends on 9-cis-RA and bexarotene, but not on all-trans-RA or an RA receptor (RAR)-selective ligand. Truncation and mutagenesis experiments demonstrated that the C-terminal LXXLL motifs in both human and sea urchin RFC3 are critical for the interaction with RXRα. The transient interaction between 9-cis-RA-activated RXRα and RFC3 resulted in reconfiguration of the PCNA-RFC complex. Furthermore, we found that knockdown of RXRα or overexpression of RFC3 impairs the ability of 9-cis-RA to inhibit proliferation of MCF-7 breast cancer cells and sea urchin embryogenesis. Our results indicate that 9-cis-RA-activated RXRα suppresses the growth of RA-sensitive breast cancer and embryonic cells through RFC3.
Oxford University Press
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