A novel specific cleavage of I κBα protein in acute myeloid leukemia cells involves protease PR3.

A novel specific cleavage of IκBα protein in acute myeloid leukemia cells involves protease PR3. Exp Cell Res. 2019 May 21;: Authors: Wang MM, Zhuang LK, Zhang YT, Xia D, Pan XR, Tong JH Abstract IκBα protein plays an important role in NFκB signaling pathway regulation. The dysfunction of IκBα is tightly related to various diseases, including cancers. However, the molecular mechanisms by which IκBα loses its normal functions are diverse and complex. Here, we reported a novel cleavage of IκBα protein occurred in AML cells. Compared with the full-length IκBα protein, the truncated IκBα fragment exhibited a dramatically weak binding ability to NFκB complex and showed a significant decreased inhibition on NFκB transactivation. Knockdown of PR3, a serine protease mainly expressed in myeloid cells, could inhibit such IκBα cleavage and enhance the sensitivities of AML cells to the differentiation inducers. In addition, we showed that the level of PR3 mRNA was relatively higher in newly diagnosed AML patients than in those patients with complete remission, suggesting that PR3 expression and its involvement in IκBα cleavage might be closely associated with AML. Our studies revealed for the first time a PR3-involved IκBα cleavage in AML cells, providing some new evidences for further understanding the mechanisms underlying the deregulation of NFκB pathway in AML. Finally, we also suggested a potential clinical applicati...
Source: Experimental Cell Research - Category: Cytology Authors: Tags: Exp Cell Res Source Type: research