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学术   教育   2024-09-18 09:48   浙江  


Mol Ther Nucleic Acids




2019 Sep 6:17:455-464.

 doi: 10.1016/j.omtn.2019.04.030. Epub 2019 Jun 7.

lncRNA SPRY4-IT1 Regulates Cell Proliferation and Migration by Sponging miR-101-3p and Regulating AMPK Expression in Gastric Cancer

Shuguang Cao 1Limiao Lin 1Xuanping Xia 1Hao Wu 2

Affiliations expand

  • PMID: 31330497

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  • PMCID: PMC6646863

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  • DOI: 10.1016/j.omtn.2019.04.030

Retraction in

  • Retraction Notice to: lncRNA SPRY4-IT1 Regulates Cell Proliferation and Migration by Sponging miR-101-3p and Regulating AMPK Expression in Gastric Cancer.

    Cao S, Lin L, Xia X, Wu H.Mol Ther Nucleic Acids. 2024 May 19;35(2):102212. doi: 10.1016/j.omtn.2024.102212. eCollection 2024 Jun 11.PMID: 38784177 Free PMC article.

Abstract

Increasing evidence indicates that long noncoding RNA SPRY4 intronic transcript 1 (lncRNA SPRY4-IT1) has been reported to be associated with the progression of several cancers, but its expression level and the function of SPRY4-IT1 in the progression of gastric cancer (GC) have been rarely reported. Here we found that SPRY4-IT1 was upregulated in GC. In vitro experiments revealed that SPRY4-IT1 knockdown significantly inhibited GC cell proliferation by causing G1 arrest and promoting apoptosis, whereas SPRY4-IT1 overexpression promoted cell growth. Further functional assays indicated that SPRY4-IT1 overexpression significantly promoted cell migration and invasion. Bioinformatics analysis predicted that there is a SPRY4-IT1/miR-101-3p/AMPK axis in GC progression. A dual-luciferase reporter system validated the direct interaction of SPRY4-IT1, miR-101-3p, and AMPK. Western blot verified that the inhibition of SPRY4-IT1 decreased AMPK expression. Furthermore, silencing SPRY4-IT1 suppressed GC growth in vivo. Importantly, we demonstrated that SPRY4-IT1 was upregulated in serum exosomes from GC patients and correlated with cancer metastasis. Altogether, silencing SPRY4-IT1 suppresses the progression of GC by interacting with miR-101-3p and decreasing inhibiting AMPK expression. Taken together, our study demonstrates that SPRY4-IT1 could act as a potential therapeutic target for GC patients.

Keywords: SPRY4-IT1; ceRNA; gastric cancer; lncRNA; metastasis; therapeutic target.

参考链接:

https://pubpeer.com/publications/F8B0863E77BED4CE8D6CE10197F484



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