HTLV-1 activates YAP via NF-?B/p65 to promote oncogenesis.

Adult T-cell leukemia/lymphoma (ATL) is an aggressive malignancy caused by human T-cell leukemia virus type 1 (HTLV-1) infection. HTLV-1 exerts its oncogenic functions by interacting with signaling pathways involved in cell proliferation and transformation. Dysregulation of the Hippo/YAP pathway is associated with multiple cancers, including virus-induced malignancies. In the present ...
study, we observe that expression of YAP, which is the key effector of Hippo signaling, is elevated in ATL cells by the action of the HTLV-1 Tax protein. YAP transcriptional activity is remarkably enhanced in HTLV-1-infected cells and ATL patients. In addition, Tax activates the YAP protein via a mechanism involving the NF-?B/p65 pathway. As a mechanism for this cross talk between the Hippo and NF-?B pathways, we found that p65 abrogates the interaction between YAP and LATS1, leading to suppression of YAP phosphorylation, inhibition of ubiquitination-dependent degradation of YAP, and YAP nuclear accumulation. Finally, knockdown of YAP suppresses the proliferation of ATL cells in vitro and tumor formation in ATL-engrafted mice. Taken together, our results suggest that p65-induced YAP activation is essential for ATL pathogenesis and implicate YAP as a potential therapeutic target for ATL treatment.
Mesh Terms:
Carcinogenesis, Cell Cycle Proteins, Cell Nucleus, Cell Proliferation, Gene Products, tax, Human T-lymphotropic virus 1, Humans, Jurkat Cells, NF-kappa B, Phosphorylation, Transcription Factors, Ubiquitination, Up-Regulation
Proc Natl Acad Sci U S A
Date: Dec. 01, 2021
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