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Title:
RNA-binding protein IGF2BP2 enhances circ_0000745 abundancy and promotes aggressiveness and stemness of ovarian cancer cells via the microRNA-3187-3p/ERBB4/PI3K/AKT axis | Journal of Ovarian Research
Description:
Background Circular RNAs (circRNAs) are increasingly recognized as important regulators in cancer including ovarian cancer (OC). This work focuses on the effects of circ_0000745 on the OC development of and molecules involved. Methods Expression of circ_0000745 in collected OC tissues and the acquired OC cell lines was examined by RT-qPCR. The stability of circ_0000745 in cells was examined by RNase R treatment. The target transcripts interacted with circ_0000745 were predicted using bioinformatic systems. Gain- and loss-of-function studies of circ_0000745, microRNA (miR)-3187-3p and erb-b2 receptor tyrosine kinase 4 (ERBB4) were conducted to determine their functions on proliferation, migration, invasion and stem cell property of OC cells. Results Circ_0000745 and ERBB4 were abundantly expressed while miR-3187-3p was poorly expressed in OC tissues and cells. Circ_0000745 sequestered miR-3187-3p and blocked its repressive effect on ERBB4. Downregulation of circ_0000745 reduced proliferation, aggressiveness, epithelial-mesenchymal transition, and stemness of SK-OV-3 cells, but this reduction was blocked upon miR-3187-3p inhibition or ERBB4 upregulation. By contrast, artificial induction of circ_0000745 upregulation, miR-3187-3p upregulation and ERBB4 downregulation led to inverse trends in ES-2 cells. ERBB4 promoted the phosphorylation of the PI3K/AKT signaling pathway. An RNA binding protein IGF2BP2 was found to circ_0000745 bind to and promote its expression and stability. Conclusion This study demonstrated that circ_0000745 upregulated by IGF2BP2 promotes aggressiveness and stemness of OC cells through a miR-3187-3p/ERBB4/PI3K/AKT axis. Circ_0000745 may serve as a promising target for OC treatment.
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Keywords {🔍}
cells, circ, erbb, expression, mirp, fig, cancer, skov, examined, assay, igfbp, cell, article, rtqpcr, ovarian, tissues, google, scholar, hainan, proliferation, suggested, rna, formation, patients, oecirc, cas, protein, binding, analysis, data, tumor, ability, anova, upregulation, found, reported, pathway, transfection, shigfbp, analyzed, luciferase, correlation, confirmed, collected, stem, hospital, wang, reduced, pikakt, mrna,
Topics {✒️}
oe-circ/sh-circ/mir-mimic/mir-inhibitor transfection examined pce-rb-mam vector-based overexpression microrna-3187-3p/erbb4/pi3k/akt axis pexp-rb-mam-based vector mir-3187-3p/erbb4/pi3k/akt axis pi3k/akt/mtor signaling pathway regulating mir-409-3p/atf1 axis similar erbb4/pi3k/akt axis subsequent erbb4/pi3k/akt axis pi3k/akt/mtor pathway pi3k/akt signaling pathway 120 mg/kg pentobarbital sodium p-phosphatidyl inositol 3-kinase regulating mir-136/cbx2 axis goat anti-rabbit igg p-pi3kinase p85 alpha sigma-aldrich chemical company life-threatening gynecologic tumors article download pdf mir mimic/inhibitor examined mir-3187-3p/erbb4 axis ultra-low attachment plates sk-ov-3 cells detected sk-ov-3 cells determined 200 μl serum-free medium chunbo hao wrote epithelial marker e-cadherin higher mir-3187-3p abundancy ovarian research aims sh-circ transfection determined sk-ov-3 cell line rna binding proteins pi3k/akt pathway closed loop structure oe-circ + sh-nc circ_0000745 sequestered mir-3187-3p circ_0000745 sequesters mir-3187-3p oe-circ +nc mimic sponging mir-106a sk-ov-3 cells led acquire chemo-resistance due sk-ov-3 cells examined sk-ov-3 cells elevated sk-ov-3 cells measured sh-igf2bp2 transfections determined sh-igf2bp2 + oe-nc hidden rna language p-protein kinase sh-igf2bp2 + oe-circ mir-3187-3p inhibitor
Questions {❓}
- A ceRNA hypothesis: the Rosetta stone of a hidden RNA language?
- Does circular RNA exert significant effects in ovarian Cancer?
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headline:RNA-binding protein IGF2BP2 enhances circ_0000745 abundancy and promotes aggressiveness and stemness of ovarian cancer cells via the microRNA-3187-3p/ERBB4/PI3K/AKT axis
description:Circular RNAs (circRNAs) are increasingly recognized as important regulators in cancer including ovarian cancer (OC). This work focuses on the effects of circ_0000745 on the OC development of and molecules involved. Expression of circ_0000745 in collected OC tissues and the acquired OC cell lines was examined by RT-qPCR. The stability of circ_0000745 in cells was examined by RNase R treatment. The target transcripts interacted with circ_0000745 were predicted using bioinformatic systems. Gain- and loss-of-function studies of circ_0000745, microRNA (miR)-3187-3p and erb-b2 receptor tyrosine kinase 4 (ERBB4) were conducted to determine their functions on proliferation, migration, invasion and stem cell property of OC cells. Circ_0000745 and ERBB4 were abundantly expressed while miR-3187-3p was poorly expressed in OC tissues and cells. Circ_0000745 sequestered miR-3187-3p and blocked its repressive effect on ERBB4. Downregulation of circ_0000745 reduced proliferation, aggressiveness, epithelial-mesenchymal transition, and stemness of SK-OV-3 cells, but this reduction was blocked upon miR-3187-3p inhibition or ERBB4 upregulation. By contrast, artificial induction of circ_0000745 upregulation, miR-3187-3p upregulation and ERBB4 downregulation led to inverse trends in ES-2 cells. ERBB4 promoted the phosphorylation of the PI3K/AKT signaling pathway. An RNA binding protein IGF2BP2 was found to circ_0000745 bind to and promote its expression and stability. This study demonstrated that circ_0000745 upregulated by IGF2BP2 promotes aggressiveness and stemness of OC cells through a miR-3187-3p/ERBB4/PI3K/AKT axis. Circ_0000745 may serve as a promising target for OC treatment.
datePublished:2021-11-13T00:00:00Z
dateModified:2021-11-13T00:00:00Z
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Ovarian cancer
IGF2BP2
circ_0000745
miR-3187-3p
ERBB4
PI3K/AKT
Gynecology
Reproductive Medicine
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headline:RNA-binding protein IGF2BP2 enhances circ_0000745 abundancy and promotes aggressiveness and stemness of ovarian cancer cells via the microRNA-3187-3p/ERBB4/PI3K/AKT axis
description:Circular RNAs (circRNAs) are increasingly recognized as important regulators in cancer including ovarian cancer (OC). This work focuses on the effects of circ_0000745 on the OC development of and molecules involved. Expression of circ_0000745 in collected OC tissues and the acquired OC cell lines was examined by RT-qPCR. The stability of circ_0000745 in cells was examined by RNase R treatment. The target transcripts interacted with circ_0000745 were predicted using bioinformatic systems. Gain- and loss-of-function studies of circ_0000745, microRNA (miR)-3187-3p and erb-b2 receptor tyrosine kinase 4 (ERBB4) were conducted to determine their functions on proliferation, migration, invasion and stem cell property of OC cells. Circ_0000745 and ERBB4 were abundantly expressed while miR-3187-3p was poorly expressed in OC tissues and cells. Circ_0000745 sequestered miR-3187-3p and blocked its repressive effect on ERBB4. Downregulation of circ_0000745 reduced proliferation, aggressiveness, epithelial-mesenchymal transition, and stemness of SK-OV-3 cells, but this reduction was blocked upon miR-3187-3p inhibition or ERBB4 upregulation. By contrast, artificial induction of circ_0000745 upregulation, miR-3187-3p upregulation and ERBB4 downregulation led to inverse trends in ES-2 cells. ERBB4 promoted the phosphorylation of the PI3K/AKT signaling pathway. An RNA binding protein IGF2BP2 was found to circ_0000745 bind to and promote its expression and stability. This study demonstrated that circ_0000745 upregulated by IGF2BP2 promotes aggressiveness and stemness of OC cells through a miR-3187-3p/ERBB4/PI3K/AKT axis. Circ_0000745 may serve as a promising target for OC treatment.
datePublished:2021-11-13T00:00:00Z
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Ovarian cancer
IGF2BP2
circ_0000745
miR-3187-3p
ERBB4
PI3K/AKT
Gynecology
Reproductive Medicine
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