| Literature DB >> 29501744 |
Xiangchou Yang1, Haihao Ye2, Muqing He1, Xiaohai Zhou1, Ni Sun1, Wenjian Guo1, Xiaoji Lin1, He Huang1, Ying Lin1, Rongxin Yao1, Hong Wang3.
Abstract
Multiple myeloma (MM), the second most common hematologic malignancy, is an incurable disease characterized by the accumulation of malignant plasma cells within the bone marrow. Though great progresses have been made in understanding the mechanisms of MM, metabolic plasticity and drug resistance remain largely unknown. In this study, we found lncRNA Protein disulfide isomerase family A member 3 pseudogene 1 (PDIA3P) is highly expressed in MM and is associated with the survival rate of MM patients. PDIA3P regulates MM growth and drug resistance through Glucose 6-phosphate dehydrogenase (G6PD) and the pentose phosphate pathway (PPP). Mechanistically, we revealed that PDIA3P interacts with c-Myc to enhance its transactivation activity and binding to G6PD promoter, stimulating G6PD expression and PPP flux. Our study identified PDIA3P as a novel c-Myc interacting lncRNA and elucidated crucial roles for PDIA3P in metabolic regulation of MM, providing a potential therapeutic target for MM patients.Entities:
Keywords: Drug resistance; G6PD; Multiple myeloma; PDIA3P; Pentose phosphate pathway; c-Myc
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Year: 2018 PMID: 29501744 DOI: 10.1016/j.bbrc.2018.02.211
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575