4.6 Article

LncRNA PDIA3P interacts with c-Myc to regulate cell proliferation via induction of pentose phosphate pathway in multiple myeloma

期刊

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2018.02.211

关键词

PDIA3P; c-Myc; Multiple myeloma; Drug resistance; G6PD; Pentose phosphate pathway

资金

  1. Lin He's New Medicine and Clinical Translation Academician Workstation Research Fund [17331208]
  2. Wenzhou Science and Technology Bureau Programs [H2015006, Y20170322]
  3. Programs of Administration of Traditional Chinese Medicine in Zhejiang [2015ZB077, 2018ZB080]

向作者/读者索取更多资源

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. (C) 2018 Elsevier Inc. All rights reserved.

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