MicroRNA-520/373 family functions as a tumor suppressor in estrogen receptor negative breast cancer by targeting NF-kappa B and TGF-beta signaling pathways

作者：Keklikoglou I^*; Koerner C; Schmidt C; Zhang J D; Heckmann D; Shavinskaya A; Allgayer H; Gueckel B; Fehm T; Schneeweiss A; Sahin Oe; Wiemann S; Tschulena U

来源：Oncogene, 2012, 31(37): 4150-4163.

DOI：10.1038/onc.2011.571

• NF-kappaB
• TGF-beta
• miR-373
• miR-520c
• breast cancer
• ER-negative

MicroRNAs (miRNAs) as modulators of gene expression have been described to display both tumor-promoting and tumor-suppressive functions. Although their role has been studied in different tumor types, little is known about how they regulate nuclear factor kappa B (NF-kappa B) signaling in breast cancer. Here, we performed an unbiased whole genome miRNA (miRome) screen to identify novel modulators of NF-kappa B pathway in breast cancer. The screen identified 13 miRNA families whose members induced consistent effects on NF-kappa B activity. Among those, the miR-520/373 family inhibited NF-kappa B signaling through direct targeting of RELA and thus strongly reduced expression and secretion of the pro-inflammatory cytokines interleukin (IL)-6 and IL-8. With a combination of in vitro and in vivo approaches, we propose a metastasis-suppressive role of miR-520/373 family. miR-520c and miR-373 abrogated both in vitro cell invasion and in vivo intravasation of highly invasive MDA-MB-231 cells. However, knockdown of RELA did not affect their metastatic ability. mRNA profiling of MDA-MB-231 cells on overexpression of miR-520/373 members revealed a strong downregulation of transforming growth factor-beta (TGF-beta) signaling. Mechanistically, the metastasis-suppressive role of miR-520/373 can be attributed to direct suppression of TGFBR2, as the silencing of TGFBR2 phenocopied the effects of miR-520/373 overexpression on suppression of Smad-dependent expression of the metastasis-promoting genes parathyroid hormone-related protein, plasminogen activator inhibitor-1 and angiopoietin-like 4 as well as tumor cell invasion, in vitro and in vivo. A negative correlation between miR-520c and TGFBR2 expression was observed in estrogen receptor negative (ER-) breast cancer patients but not in the ER positive (ER+) subtype. Remarkably, decreased expression of miR-520c correlated with lymph node metastasis specifically in ER- tumors. Taken together, our findings reveal that miR-520/373 family has a tumor-suppressive role in ER- breast cancer by acting as a link between the NF-kappa B and TGF-beta pathways and may thus contribute to the interplay of tumor progression, metastasis and inflammation. Oncogene (2012) 31, 4150-4163; doi:10.1038/onc.2011.571; published online 12 December 2011

• 出版日期2012-9