A long non-coding RNA TSLD8 inhibits hepatocellular carcinoma by stabilizing WWOX

被引:4
作者
Xu, Fengliang [1 ]
Wang, Botian [2 ]
Liu, Mingxia [2 ]
Liu, Tao [3 ]
Zhang, Ronghua [1 ]
机构
[1] Peoples Hosp Rizhao, Dept Lab, 126 Taian Rd, Rizhao 276826, Shandong, Peoples R China
[2] Chinese Med Hosp Rizhao, Dept Lab, Rizhao 276800, Shandong, Peoples R China
[3] Chinese Med Hosp Rizhao, Dept Pharm, Rizhao 276800, Shandong, Peoples R China
关键词
LncRNA; TSLD8; WWOX; HCC; TUMOR-SUPPRESSOR; GENE; CANCER; DELIVERY; METASTASIS; EXPRESSION; PULLULAN; POLYMERS; THERAPY; LNCRNA;
D O I
10.1016/j.bbrc.2019.06.043
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
The hepatocellular carcinoma (HCC) is a common and highly aggressive malignancy especially in China. Accumulating data have shown a critical role of long non-coding RNAs (lncRNAs) during cancer progression. However, the function of IncRNA TSLD8 remains elusive. By IncRNA profiling, we identify a novel IncRNA termed TSLD8 in HCC. TSLD8 expression is significantly lowered in HCC tissues and cell lines. TSLD8 facilitates migration and viability in SMMC-7721 and HepG2 cells. Furthermore, TSLD8 can interact with WWOX and protect WWOX from proteasome-mediated degradation. Using PuPGEA-based nanocomplex for gene delivery, we found that co-delivery of TSLD8 and WWOX may exhibit synergistic and additive effects to inhibit HCC progression. PuPGEA-based nanocomplex delivery does not substantially alter the blood chemistries (e.g. alkaline phosphatase, blood urea nitrogen, aspartate aminotransferase, alanine aminotransferase) or initiate immune responses implying a safe strategy. Collectively, our current study has identified a novel tumor suppressive IncRNA TSLD8 which exerts its tumor suppressive function by stabilizing WWOX. Co-delivery of TSLD8 and WWOX via PuPGEA-based nanocomplexes might provide promising therapeutics for eradicating HCC. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:526 / 532
页数:7
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