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Title:
IGF2BP3 enhances the mRNA stability of E2F3 by interacting with LINC00958 to promote endometrial carcinoma progression | Cell Death Discovery
Description:
Long noncoding RNAs (lncRNAs) play important regulatory roles in a variety of pathological processes involving cancer. However, the exact molecular mechanisms of lncRNA regulation in endometrial carcinoma (EC) remain poorly defined. The aim of this study was to illustrate the mechanism of LINC00958 in regulating the function of IGF2BP3, an RNA binding protein involved in mRNA stability, and their clinical implications in EC. First, we investigated the clinical role of IGF2BP3 in EC and demonstrated its prognostic value. Loss-of-function and gain-of-function studies showed that IGF2BP3 promoted EC cell proliferation, migration and invasion. Then, we carried out RNA immunoprecipitation sequencing (RIP-seq) analysis, RNA pulldown and immunofluorescence-RNA fluorescence in situ hybridization to identify LINC00958 that interacted with IGF2BP3 in the cytoplasm of EC cells. Rescue experiments indicated that knockdown of LINC00958 partially offset the EC cell progression mediated by IGF2BP3. After that, RNA sequencing was used to screen out the downstream genes of IGF2BP3 and LINC00958. The results revealed that IGF2BP3 upregulated E2F3 expression by interacting with LINC00958. Furthermore, RNA stability assays demonstrated that silencing LINC00958 partially rescued the IGF2BP3-mediated promoting effect on the mRNA stability of E2F3. Collectively, this study suggests that LINC00958, as an oncogene, assists IGF2BP3 in stabilizing E2F3 mRNA and ultimately promotes EC progression, providing a promising therapeutic target for patients with EC.
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nature portfolio privacy policy fgf13-as1/igf2bps/myc feedback loop wnt/ฮฒ-catenin signaling regulates nature hmga2-tgf-beta/wnt pathway advertising generated protein-rna-bead compounds web tools based social media facilitate cancer development outstanding scientific fund affects pi3k/akt pathway portal reprints middle japan research lncrna-rmrp/znrf3 axis lncrna cdkn2b-as1 stabilized maternal-fetal medicine thermo scientific dual-luciferase reporter plasmid mir-145-3p/tcf4 axis [21] mir-145-3p/tcf4 axis cdk4/rb/e2fs axis original author lnc942 promoting mettl14-mediated author information authors regulating e2f3/mapk8 signaling lncrna-lnc942 directly recruited anti-igf2bp3 primary antibody table s1 hairpin-derived small rnas table s2 selectable statistical methods 415-nt wild-type sequence integrated optical density/area added 5โยตg/ml actinomycin cell death dis cell death discov linc00958/mir-3174/phf6 axis full size image paraffin-embedded clinical specimens kaplanโmeier plot obtained long noncoding rnas c-myc mrna stability rtโqpcr assays showed lncrna cdkn2b-as1 imp-3 promotes migration
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- Insulin-like growth factor 2 mRNA-binding proteins (IGF2BPs): post-transcriptional drivers of cancer progression?
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headline:IGF2BP3 enhances the mRNA stability of E2F3 by interacting with LINC00958 to promote endometrial carcinoma progression
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headline:IGF2BP3 enhances the mRNA stability of E2F3 by interacting with LINC00958 to promote endometrial carcinoma progression
description:Long noncoding RNAs (lncRNAs) play important regulatory roles in a variety of pathological processes involving cancer. However, the exact molecular mechanisms of lncRNA regulation in endometrial carcinoma (EC) remain poorly defined. The aim of this study was to illustrate the mechanism of LINC00958 in regulating the function of IGF2BP3, an RNA binding protein involved in mRNA stability, and their clinical implications in EC. First, we investigated the clinical role of IGF2BP3 in EC and demonstrated its prognostic value. Loss-of-function and gain-of-function studies showed that IGF2BP3 promoted EC cell proliferation, migration and invasion. Then, we carried out RNA immunoprecipitation sequencing (RIP-seq) analysis, RNA pulldown and immunofluorescence-RNA fluorescence in situ hybridization to identify LINC00958 that interacted with IGF2BP3 in the cytoplasm of EC cells. Rescue experiments indicated that knockdown of LINC00958 partially offset the EC cell progression mediated by IGF2BP3. After that, RNA sequencing was used to screen out the downstream genes of IGF2BP3 and LINC00958. The results revealed that IGF2BP3 upregulated E2F3 expression by interacting with LINC00958. Furthermore, RNA stability assays demonstrated that silencing LINC00958 partially rescued the IGF2BP3-mediated promoting effect on the mRNA stability of E2F3. Collectively, this study suggests that LINC00958, as an oncogene, assists IGF2BP3 in stabilizing E2F3 mRNA and ultimately promotes EC progression, providing a promising therapeutic target for patients with EC.
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name:Key Laboratory of Maternal-Fetal Medicine of Liaoning Province, Department of Obstetrics and Gynecology, Shengjing Hospital Affiliated to China Medical University, Shenyang, PR China
name:Department of Obstetrics and Gynecology, Shengjing Hospital Affiliated to China Medical University, Shenyang, PR China
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name:Department of Obstetrics and Gynecology, Shengjing Hospital Affiliated to China Medical University, Shenyang, PR China
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name:Department of Obstetrics and Gynecology, Shengjing Hospital Affiliated to China Medical University, Shenyang, PR China
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name:Department of Obstetrics and Gynecology, Shengjing Hospital Affiliated to China Medical University, Shenyang, PR China
name:Key Laboratory of Gynecological Oncology of Liaoning Province, Department of Obstetrics and Gynecology, Shengjing Hospital Affiliated to China Medical University, Shenyang, PR China
name:Key Laboratory of Maternal-Fetal Medicine of Liaoning Province, Department of Obstetrics and Gynecology, Shengjing Hospital Affiliated to China Medical University, Shenyang, PR China
name:Department of Obstetrics and Gynecology, Shengjing Hospital Affiliated to China Medical University, Shenyang, PR China
name:Key Laboratory of Gynecological Oncology of Liaoning Province, Department of Obstetrics and Gynecology, Shengjing Hospital Affiliated to China Medical University, Shenyang, PR China
name:Key Laboratory of Maternal-Fetal Medicine of Liaoning Province, Department of Obstetrics and Gynecology, Shengjing Hospital Affiliated to China Medical University, Shenyang, PR China
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CDN Services {๐ฆ}
- Crossref