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Novel Interleukin-6 Inducible Gene PDZ-Binding Kinase Promotes Tumor Growth of Multiple Myeloma Cells.


ABSTRACT: [Figure: see text] Multiple myeloma (MM) remains an intractable hematological malignancy, despite recent advances in anti-MM drugs. Here, we show that role of PDZ binding kinase (PBK) in MM tumor growth. We identified that interleukin-6 (IL-6) readily increases PBK expression. Kaplan-Meier analysis showed that the MM patients with higher expression of PBK have a significant shorter survival time compared with those with moderate/lower expression of PBK. Knockout of PBK dramatically suppressed in vivo tumor growth in MM cells, while genome editing of PBK changing from asparagine to serine substitution (rs3779620) slightly suppresses the tumor formation. Mechanistically, loss of PBK increased the number of apoptotic cells with concomitant decrease in the phosphorylation level of Stat3 as well as caspase activities. A novel PBK inhibitor OTS514 significantly decreased KMS-11-derived tumor growth. These findings highlight the novel oncogenic role of PBK in tumor growth of myeloma, and it might be a novel therapeutic target for the treatment of patients with MM.

SUBMITTER: Ota A 

PROVIDER: S-EPMC7462034 | biostudies-literature | 2020 Aug

REPOSITORIES: biostudies-literature

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Novel Interleukin-6 Inducible Gene PDZ-Binding Kinase Promotes Tumor Growth of Multiple Myeloma Cells.

Ota Akinobu A   Hanamura Ichiro I   Karnan Sivasundaram S   Inaguma Shingo S   Takei Norio N   Lam Vu Quang VQ   Mizuno Shohei S   Kanasugi Jo J   Wahiduzzaman Md M   Rahman Md Lutfur ML   Hyodo Toshinori T   Konishi Hiroyuki H   Tsuzuki Shinobu S   Ikeda Hiroshi H   Takami Akiyoshi A   Hosokawa Yoshitaka Y  

Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research 20200723 8


[Figure: see text] Multiple myeloma (MM) remains an intractable hematological malignancy, despite recent advances in anti-MM drugs. Here, we show that role of PDZ binding kinase (PBK) in MM tumor growth. We identified that interleukin-6 (IL-6) readily increases PBK expression. Kaplan-Meier analysis showed that the MM patients with higher expression of PBK have a significant shorter survival time compared with those with moderate/lower expression of PBK. Knockout of <i>PBK</i> dramatically suppre  ...[more]

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