1. Hypoxia-induced long non-coding RNA DARS-AS1 regulates RBM39 stability to promote myeloma malignancy
- Author
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Rufang Xiang, Chao Wu, Hua Yan, Zilu Zhang, Ying-Li Wu, Chengning Ma, Junmin Li, Wenbin Xu, Fenghuang Zhan, Jia Tong, Jia Liu, and Xiaoguang Xu
- Subjects
medicine.disease_cause ,Plasma Cell Disorders ,Downregulation and upregulation ,Cell Line, Tumor ,hemic and lymphatic diseases ,parasitic diseases ,Tumor Microenvironment ,medicine ,Humans ,Hypoxia ,Multiple myeloma ,Gene knockdown ,biology ,Chemistry ,fungi ,Articles ,Hematology ,medicine.disease ,Ubiquitin ligase ,medicine.anatomical_structure ,Hypoxia-inducible factors ,biology.protein ,Cancer research ,RNA, Long Noncoding ,Bone marrow ,Signal transduction ,Multiple Myeloma ,Carcinogenesis ,Signal Transduction - Abstract
Multiple myeloma is a malignant plasma-cell disease, which is highly dependent on the hypoxic bone marrow microenvironment. However, the underlying mechanisms of hypoxia contributing to myeloma genesis are not fully understood. Here, we show that long non-coding RNA DARS-AS1 in myeloma is directly upregulated by hypoxia inducible factor (HIF)-1. Importantly, DARS-AS1 is required for the survival and tumorigenesis of myeloma cells both in vitro and in vivo. DARS-AS1 exerts its function by binding RNA-binding motif protein 39 (RBM39), which impedes the interaction between RBM39 and its E3 ubiquitin ligase RNF147, and prevents RBM39 from degradation. The overexpression of RBM39 observed in myeloma cells is associated with poor prognosis. Furthermore, knockdown of DARS-AS1 inhibits the mammalian target of rapamycin signaling pathway, an effect that is reversed by RBM39 overexpression. We reveal that a novel HIF-1/DARS-AS1/RBM39 pathway is implicated in the pathogenesis of myeloma. Targeting DARS-AS1/RBM39 may, therefore, represent a novel strategy to combat myeloma.
- Published
- 2019
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