[PDF][PDF] Polycomb-mediated loss of miR-31 activates NIK-dependent NF-κB pathway in adult T cell leukemia and other cancers

M Yamagishi, K Nakano, A Miyake, T Yamochi… - Cancer cell, 2012 - cell.com
M Yamagishi, K Nakano, A Miyake, T Yamochi, Y Kagami, A Tsutsumi, Y Matsuda…
Cancer cell, 2012cell.com
Constitutive NF-κB activation has causative roles in adult T cell leukemia (ATL) caused by
HTLV-1 and other cancers. Here, we report a pathway involving Polycomb-mediated miRNA
silencing and NF-κB activation. We determine the miRNA signatures and reveal miR-31 loss
in primary ATL cells. MiR-31 negatively regulates the noncanonical NF-κB pathway by
targeting NF-κB inducing kinase (NIK). Loss of miR-31 therefore triggers oncogenic
signaling. In ATL cells, miR-31 level is epigenetically regulated, and aberrant upregulation …
Summary
Constitutive NF-κB activation has causative roles in adult T cell leukemia (ATL) caused by HTLV-1 and other cancers. Here, we report a pathway involving Polycomb-mediated miRNA silencing and NF-κB activation. We determine the miRNA signatures and reveal miR-31 loss in primary ATL cells. MiR-31 negatively regulates the noncanonical NF-κB pathway by targeting NF-κB inducing kinase (NIK). Loss of miR-31 therefore triggers oncogenic signaling. In ATL cells, miR-31 level is epigenetically regulated, and aberrant upregulation of Polycomb proteins contribute to miR-31 downregulation in an epigenetic fashion, leading to activation of NF-κB and apoptosis resistance. Furthermore, this emerging circuit operates in other cancers and receptor-initiated NF-κB cascade. Our findings provide a perspective involving the epigenetic program, inflammatory responses, and oncogenic signaling.
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