PHLDA1 expression is controlled by an estrogen receptor-NFκB-miR-181 regulatory loop and is essential for formation of ER+ mammospheres

• Published in: Oncogene 2015-04, Vol.34 (18), p.2309-2316
• Main Authors: Kastrati, I, Canestrari, E, Frasor, J
• Format: Article
• Language: English
• Subjects: 13/100; 13/106; 13/109; 13/21; 17β-Estradiol; 3' Untranslated regions; 38/77; 38/90; 631/67/1347; 82/80; Aldehyde dehydrogenase; Apoptosis; Breast cancer; Breast Neoplasms - genetics; Breast Neoplasms - metabolism; Breast Neoplasms - pathology; Cell Biology; Cell Line, Tumor; Cell survival; Estrogen; Estrogen receptors; Female; Gene expression; Gene Expression Regulation, Neoplastic; Gene silencing; Health aspects; Homology; Human Genetics; Humans; Inflammation; Internal Medicine; Intestine; MCF-7 Cells; Medicine; Medicine & Public Health; Metastases; MicroRNAs - genetics; mRNA stability; Neoplastic Stem Cells - metabolism; NF-kappa B - metabolism; NF-κB protein; Oncology; original-article; Overexpression; Phenotypes; Pleckstrin; Post-transcription; Receptors; Receptors, Estrogen - metabolism; Signal Transduction; Stem cells; Transcription Factors - genetics; Transcription Factors - metabolism; Transplantation; Tumor necrosis factor-α; Tumorigenesis; Tumors
• ISSN: 0950-9232; 1476-5594
• DOI: 10.1038/onc.2014.180

Crosstalk between estrogen receptor (ER) and the inflammatory nuclear factor κB (NFκB) pathway in ER+ breast cancers may contribute to a more aggressive phenotype. Pleckstrin Homology-Like Domain, Family A, member 1 (PHLDA1), a target gene of ER-NFκB crosstalk, has been implicated in cell survival and stem cell properties. 17β-estradiol (E2), acting through ERα, and pro-inflammatory cytokines, acting through NFκB, increase the nascent transcript and PHLDA1 messenger RNA stability, indicating both transcriptional and post-transcriptional control of PHLDA1 expression. We show that PHLDA1 is a direct target of miR-181 and that mature miR-181a and b, as well as their host gene, are synergistically downregulated by E2 and tumor necrosis factor α, also in an ER- and NFκB-dependent manner. Thus, ER and NFκB work together to upregulate PHLDA1 directly through enhanced transcription and indirectly through repression of miR-181a and b. Previous studies have suggested that PHLDA1 may be a stem cell marker in the human intestine that contributes to tumorigenesis. Our findings that PHLDA1 is upregulated in mammospheres (MS) of ER+ breast cancer cells and that PHLDA1 knockdown impairs both MS formation and the expansion of aldehyde dehydrogenase (ALDH)-positive population, suggest that PHLDA1 may play a similar role in breast cancer cells. Upregulation of PHLDA1 in MS is largely dependent on the NFκB pathway, with downregulated miR-181 expression a contributing factor. Over-expression of miR-181 phenocopied PHLDA1 knockdown and significantly impaired MS formation, which was reversed, in part, by protection of the PHLDA1 3′ untranslated region (UTR) or overexpression of PHLDA1 lacking the 3′UTR. Furthermore, we find that elevated PHLDA1 expression is associated with a higher risk of distant metastasis in ER+ breast cancer patients. Altogether, these data suggest that high PHLDA1 expression is controlled through an ER-NFκB-miR-181 regulatory axis and may contribute to a poor clinical outcome in patients with ER+ breast tumors by enhancing stem-like properties in these tumors.