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10.1038/s41419-018-0643-5

http://scihub22266oqcxt.onion/10.1038/s41419-018-0643-5
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suck abstract from ncbi


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pmid29789536
      Cell+Death+Dis 2018 ; 9 (6 ): 607
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  • Long noncoding RNA gastric cancer-related lncRNA1 mediates gastric malignancy through miRNA-885-3p and cyclin-dependent kinase 4 #MMPMID29789536
  • Lin Z ; Zhou Z ; Guo H ; He Y ; Pang X ; Zhang X ; Liu Y ; Ao X ; Li P ; Wang J
  • Cell Death Dis 2018[May]; 9 (6 ): 607 PMID29789536 show ga
  • Gastric cancer (GC) is one of the most common malignancy and the third leading cancer-related death in China. Long noncoding RNAs (lncRNAs) have been implicated in numerous tumors, including GC, however, the mechanism of many functional lncRNAs is still unclear. In this study, we identified the abundantly expressed lncRNA, RP11-290F20.3, in GC cells and patient tumor tissues. We named this lncRNA as GC-related lncRNA1 (GCRL1), which could regulate gastric cell proliferation and metastasis, both in vitro and in vivo. Mechanistically, miRNA-885-3p (miR-885-3p) could inhibit the cell proliferation and metastasis in GC by negatively regulating the expression of cyclin-dependent kinase 4 (CDK4) at the post-transcriptional level. Further, GCRL1 promoted the cell proliferation and metastasis by sponging miR-885-3p and hence, positively regulating CDK4 in GC cells. Taken together, our results demonstrate a novel regulatory axis of malignant cell proliferation and invasion in GC, comprising GCRL1, miR-885-3p, and CDK4, which may serve as a potential therapeutic target in GC.
  • |Base Sequence [MESH]
  • |Cell Line, Tumor [MESH]
  • |Cell Movement/genetics [MESH]
  • |Cell Proliferation/genetics [MESH]
  • |Cyclin-Dependent Kinase 4/*metabolism [MESH]
  • |Gene Expression Regulation, Neoplastic [MESH]
  • |Humans [MESH]
  • |MicroRNAs/genetics/*metabolism [MESH]
  • |Neoplasm Invasiveness [MESH]
  • |Neoplasm Metastasis [MESH]
  • |RNA, Long Noncoding/genetics/*metabolism [MESH]
  • |Stomach Neoplasms/*genetics/*pathology [MESH]


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