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Pim2 is required for maintaining multiple myeloma cell growth through modulating TSC2 phosphorylation

Lu, Jing and Zavorotinskaya, Tatiana and Dai, Yumin and Niu, Xiaohong and Castillo, Joseph and Sim, Janet and Yu, Jianjun and Wang, Yingyun and Langowski, John and Holash, Jocelyn and Shannon, Kevin and Garcia, Pablo (2013) Pim2 is required for maintaining multiple myeloma cell growth through modulating TSC2 phosphorylation. Blood, 122 (9). pp. 1610-1620. ISSN 1528-0020

Abstract

Multiple myeloma (MM) is the second most common hematologic malignancy. Despite recent treatment advances, it remains incurable. Here, we report that Pim2 kinase expression is highly elevated in MM cells and demonstrate that it is required for MM cell proliferation. Functional interference of Pim2 activity either by short hairpin RNAs or by a potent and selective small-molecule inhibitor leads to significant inhibition of MM cell proliferation. Pim inhibition results in a significant decrease of mammalian target of rapamycin C1 (mTOR-C1) activity, which is critical for cell proliferation.Weidentify TSC2, a negative regulator of mTOR-C1, as a novel Pim2 substrate and show that Pim2 directly phosphorylates TSC2 on Ser-1798 and relieves the suppression of TSC2 on mTOR-C1. These findings support Pim2 as a promising therapeutic target for MM and define a novel Pim2-TSC2-mTOR-C1 pathway that drives MM proliferation.

Item Type: Article
Date Deposited: 21 Nov 2017 00:45
Last Modified: 25 Jan 2019 00:46
URI: https://oak.novartis.com/id/eprint/10368

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