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Publication : Metastasis-Associated Protein 2 Represses NF-κB to Reduce Lung Tumor Growth and Inflammation.

First Author  El-Nikhely N Year  2020
Journal  Cancer Res Volume  80
Issue  19 Pages  4199-4211
PubMed ID  32816854 Mgi Jnum  J:296659
Mgi Id  MGI:6467625 Doi  10.1158/0008-5472.CAN-20-1158
Citation  El-Nikhely N, et al. (2020) Metastasis-Associated Protein 2 Represses NF-kappaB to Reduce Lung Tumor Growth and Inflammation. Cancer Res 80(19):4199-4211
abstractText  Although NF-kappaB is known to play a pivotal role in lung cancer, contributing to tumor growth, microenvironmental changes, and metastasis, the epigenetic regulation of NF-kappaB in tumor context is largely unknown. Here we report that the IKK2/NF-kappaB signaling pathway modulates metastasis-associated protein 2 (MTA2), a component of the nucleosome remodeling and deacetylase complex (NuRD). In triple transgenic mice, downregulation of IKK2 (Sftpc-cRaf-IKK2DN) in cRaf-induced tumors in alveolar epithelial type II cells restricted tumor formation, whereas activation of IKK2 (Sftpc-cRaf-IKK2CA) supported tumor growth; both effects were accompanied by altered expression of MTA2. Further studies employing genetic inhibition of MTA2 suggested that in primary tumor growth, independent of IKK2, MTA2/NuRD corepressor complex negatively regulates NF-kappaB signaling and tumor growth, whereas later dissociation of MTA2/NuRD complex from the promoter of NF-kappaB target genes and IKK2-dependent positive regulation of MTA2 leads to activation of NF-kappaB signaling, epithelial-mesenchymal transition, and lung tumor metastasis. These findings reveal a previously unrecognized biphasic role of MTA2 in IKK2/NF-kappaB-driven primary-to-metastatic lung tumor progression. Addressing the interaction between MTA2 and NF-kappaB would provide potential targets for intervention of tumor growth and metastasis. SIGNIFICANCE: These findings strongly suggest a prominent role of MTA2 in primary tumor growth, lung metastasis, and NF-kappaB signaling modulatory functions.
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