Zhan Ting, Cheng Xueting, Zhu Qingxi, Han Zheng, Zhu Kejing, Tan Jie, Liu Men, Chen Wei, Chen Xiaoli, Chen Xiaohong, Tian Xia, Huang Xiaodong
Department of Gastroenterology, WuHan Third Hospital (Tongren hospital of WuHan University), 430060, Wuhan, China.
Department of Pharmacy, WuHan Third Hospital (Tongren hospital of WuHan University), 430060, Wuhan, China.
Cell Death Discov. 2023 Mar 10;9(1):89. doi: 10.1038/s41420-023-01384-3.
There is growing evidence that long non-coding RNAs (lncRNAs) are significant contributors to the epigenetic mechanisms implicated in the emergence, progression and metastasis of the colorectal cancer (CRC), but many remain underexplored. A novel lncRNA LOC105369504, was identified to be a potential functional lncRNA by microarray analysis. In CRC, the expression of LOC105369504 was markedly decreased and resulted in distinct variations in proliferation, invasion, migration and epithelial-mesenchymal transition (EMT) in vivo and in vitro. This study showed that LOC105369504 bound to the protein of paraspeckles compound 1 (PSPC1) directly and regulated its stability using the ubiquitin-proteasome pathway in CRC cells. The suppression of CRC by LOC105369504 could be reversed through PSPC1 overexpression.This study showed that in CRC, LOC105369504 was under-regulated and as a novel lncRNA, LOC105369504 exerted tumor suppressive activity to suppress the proliferation together with metastasis in CRC cells through the regulation of PSPC1. These results offer new perspectives on the lncRNA effect on the progression of CRC.
越来越多的证据表明,长链非编码RNA(lncRNA)在结直肠癌(CRC)的发生、发展和转移所涉及的表观遗传机制中起着重要作用,但许多lncRNA仍未得到充分研究。通过微阵列分析,一种新的lncRNA LOC105369504被鉴定为潜在的功能性lncRNA。在CRC中,LOC105369504的表达明显降低,并在体内和体外导致增殖、侵袭、迁移和上皮-间质转化(EMT)的明显变化。本研究表明,LOC105369504直接与副斑点复合物1(PSPC1)的蛋白质结合,并在CRC细胞中使用泛素-蛋白酶体途径调节其稳定性。通过PSPC1过表达可以逆转LOC105369504对CRC的抑制作用。本研究表明,在CRC中,LOC105369504表达下调,作为一种新的lncRNA,LOC105369504通过调节PSPC1发挥肿瘤抑制活性,抑制CRC细胞的增殖和转移。这些结果为lncRNA对CRC进展的影响提供了新的视角。