Title:LINC00461 Knockdown Enhances the Effect of Ixazomib in Multiple
Myeloma Cells
Volume: 23
Issue: 8
Author(s): Mingyang Deng, Huan Yuan, Hongling Peng, Sufang Liu, Xiang Xiao, Zhihua Wang, Guangsen Zhang and Han Xiao*
Affiliation:
- Department of Neurology, the Second Xiangya Hospital, Central South University, Changsha, 410011, China
Keywords:
Multiple myeloma, ixazomib, cell apoptosis, LINC00461, SNRPB2, B2 knockdown.
Abstract:
Background: LINC00461 has been implicated to be involved in several types of cancer
while its roles in multiple myeloma remain unclear. Our study aims to investigate the roles of
LINC00461 in multiple myeloma and explore its effects on ixazomib therapy.
Methods: LINC00461 and small nuclear ribonucleoprotein polypeptide (SNRP) B2 knockdown stable
cell lines were constructed. Cell viability assays including MTT, cell number counting, and colony
formation were performed. RNA-pull down and immunoblotting assays were conducted to determine
the intramolecular interactions. qRT-PCR and western blotting were conducted to determine the levels
of target genes. Kaplan-Meier analysis was used to evaluate overall survival rates.
Results: Knockdown of LINC00461 or SNRPB2 enhanced ixazomib's cytotoxicity, as well as affected
its regulatory effects on cell apoptosis and cell cycle distribution. Further results showed that
LINC00461 knockdown reduced the expression levels of SNRPB2 by their interactions. Additionally,
a positive correlation between LINC00461 and SNRPB2 was found in patients with multiple myeloma.
Low expression of SNRPB2 was associated with a high survival rate in patients with multiple myeloma.
Conclusion: Knockdown of LINC00461 enhanced the therapeutic effects of ixazomib against multiple
myeloma in part by the regulation of SNRPB2.
