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MiR362-3p Alleviates Osteosarcoma by Regulating the IL6ST/JAK2/STAT3 Pathway in Vivo and in Vitro .
- Source :
-
Technology in cancer research & treatment [Technol Cancer Res Treat] 2024 Jan-Dec; Vol. 23, pp. 15330338241261616. - Publication Year :
- 2024
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Abstract
- Objectives: To investigate the effects and the related signaling pathway of miR-362-3p on OS. Methods: The bioinformatics analysis approaches were employed to investigate the target pathway of miR-362-3p. After the 143B and U2OS cells and nu/nu male mice were randomly divided into blank control (BC) group, normal control (NC) group, and overexpression group (OG), the CCK-8, EdU staining, wound healing assay, Transwell assay, and TUNEL staining were adopted to respectively determine the effects of overexpressed miR-362-3p on the cell viability, proliferation, migration, invasion, and apoptosis of 143B and U2OS cells in vitro , tumor area assay and hematoxylin and eosin staining were employed to respectively determine the effects of overexpressed miR-362-3p on the growth and pathological injury of OS tissue in vivo . The qRT-PCR, Western blot, and immunohistochemical staining were applied to respectively investigate the effects of overexpressed miR-362-3p on the IL6ST/JAK2/STAT3 pathway in OS in vivo and in vitro . Results: The bioinformatics analysis approaches combined qRT-PCR indicated that the IL6ST/JAK2/STAT3 is one of the target pathways of miR-362-3p. Compared with NC, the cell viability, proliferation, migration, and invasion of 143B and U2OS cells were dramatically ( P < 0.01) inhibited but the apoptosis was prominently ( P <0 .0001) promoted in OG. Compared with NC, the growth of OS tissue was significantly ( P < 0.05) suppressed and the pathological injury of OS tissue was substantially aggravated in OG. The gene expression levels of IL6ST, JAK2, and STAT3 and the protein expression levels of IL6ST, JAK2, p-JAK2, STAT3, and p-STAT3 in 143B and U2OS cells were memorably ( P < 0.0001) lower in OG than those in NC. In addition, the positively stained areas of proteins of IL6ST, JAK2, p-JAK2, STAT3, and p-STAT3 of OS tissue in OG were markedly ( P < 0.01) reduced compared with those in NC. Conclusion: The overexpression of miR362-3p alleviates OS by inhibiting the IL6ST/JAK2/STAT3 pathway in vivo and in vitro .<br />Competing Interests: Declaration of Conflicting InterestsThe authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
- Subjects :
- Humans
Animals
Mice
Cell Line, Tumor
Male
Bone Neoplasms genetics
Bone Neoplasms pathology
Bone Neoplasms metabolism
Xenograft Model Antitumor Assays
Cytokine Receptor gp130 metabolism
Cytokine Receptor gp130 genetics
Computational Biology methods
Disease Models, Animal
Cell Survival genetics
MicroRNAs genetics
STAT3 Transcription Factor metabolism
STAT3 Transcription Factor genetics
Janus Kinase 2 metabolism
Janus Kinase 2 genetics
Osteosarcoma genetics
Osteosarcoma pathology
Osteosarcoma metabolism
Signal Transduction
Cell Proliferation
Gene Expression Regulation, Neoplastic
Cell Movement genetics
Apoptosis genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1533-0338
- Volume :
- 23
- Database :
- MEDLINE
- Journal :
- Technology in cancer research & treatment
- Publication Type :
- Academic Journal
- Accession number :
- 39051528
- Full Text :
- https://doi.org/10.1177/15330338241261616