KSP inhibitor SB743921 induces death of multiple myeloma cells via inhibition of the NF-κB signaling pathway

被引:12
作者
Song, In-Sung [1 ]
Jeong, Yu Jeong [1 ]
Nyamaa, Bayalagmaa [1 ]
Jeong, Seung Hun [1 ]
Kim, Hyoung Kyu [1 ]
Kim, Nari [1 ]
Ko, Kyung Soo [1 ]
Rhee, Byoung Doo [1 ]
Han, Jin [1 ]
机构
[1] Inje Univ, Natl Res Lab Mitochondrial Signaling, Cardiovasc & Metab Dis Ctr, Dept Physiol,Coll Med, Busan 47392, South Korea
基金
新加坡国家研究基金会;
关键词
SB743921; NF-kappa B; multiple myeloma; combination therapy; superoxide dismutase 2; Mcl-1; BORTEZOMIB-RESISTANCE; APOPTOSIS; CANCER; ACTIVATION; GENE;
D O I
10.5483/BMBRep.2015.48.10.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
SB743921 is a potent inhibitor of the spindle protein kinesin and is being investigated in ongoing clinical trials for the treatment of myeloma. However, little is known about the molecular events underlying the induction of cell death in multiple myeloma (MM) by SB743921, alone or in combination treatment. Here, we report that SB743921 induces mitochondria-mediated cell death via inhibition of the NF-kappa B signaling pathway, but does not cause cell cycle arrest in KMS20 MM cells. SB743921-mediated inhibition of the NF-kappa B pathway results in reduced expression of SOD2 and Mcl-1, leading to mitochondrial dysfunction. We also found that combination treatment with SB743921 and bortezomib induces death in bortezomib-resistant KMS20 cells. Altogether, these data suggest that treatment with SB743921 alone or in combination with bortezomib offers excellent translational potential and promises to be a novel MM therapy.
引用
收藏
页码:571 / 576
页数:6
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