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pmid:35593122

MicroRNA-744-5p suppresses tumorigenesis and metastasis of osteosarcoma through the p38 mitogen-activated protein kinases pathway by targeting transforming growth factor-beta 1.

Haofeng Liang · Lin Li · Shuang Zhu · Jianye Tan · Bingsheng Yang · Xiaoping Wang · Guofeng Wu · Chao Xie · Lutao Li · Zhengwei Liu · Yucong Li · Haoqiang Song · Guoli Chen · Lijun Lin

Bioengineered · 2022 doi:10.1080/21655979.2022.2072619

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

Execution evidence has not yet been added to this .science file. Explore its methods, data and open questions to plan the next step.
Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:35593122
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science-record
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2026-11-01T18:14:29Z
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state
complete
title
MicroRNA-744-5p suppresses tumorigenesis and metastasis of osteosarcoma through the p38 mitogen-activated protein kinases pathway by targeting transforming growth factor-beta 1.
doi
10.1080/21655979.2022.2072619
pmid
35593122
authors array · 14 items
[0]
Haofeng Liang
[1]
Lin Li
[2]
Shuang Zhu
[3]
Jianye Tan
[4]
Bingsheng Yang
[5]
Xiaoping Wang
[6]
Guofeng Wu
[7]
Chao Xie
[8]
Lutao Li
[9]
Zhengwei Liu
[10]
Yucong Li
[11]
Haoqiang Song
[12]
Guoli Chen
[13]
Lijun Lin
journal
Bioengineered
year
2022
abstract
Osteosarcoma (OS) is the most common malignant bone tumor in children and adolescents. Accumulating evidence has revealed that microRNAs (miRNAs) play a crucial role in the progression of OS. In this study, we found that miR-744-5p was the least expressed miRNA in patients with OS by analyzing GSE65071 from the GENE EXPRESSION OMNIBUS (GEO) database. Through real-time quantitative PCR (qRT-PCR), western blotting, colony formation assay, 5-Ethynyl-2-Deoxyuridine (EdU) incorporation assay, transwell migration, and invasion assays, we demonstrated its ability to inhibit the proliferation, migration, and invasion of OS cells in vitro. According to the luciferase reporter assay, transforming growth factor-β1 (TGFB1) was negatively regulated by miR-744-5p and reversed the effects of miR-744-5p on OS. Subcutaneous tumor-forming animal models and tail vein injection lung metastatic models were used in animal experiments, and it was found that miR-744-5p negatively regulated tumor growth and metastasis in vivo. Furthermore, rescue assays verified that miR-744-5p regulates TGFB1 expression in OS. Further experiments revealed that the p38 MAPK signaling pathway is involved in the miR-744-5p/TGFB1 axis. Generally, this study suggests that miR-744-5p is a negative regulator of TGFB1 and suppresses OS progression and metastasis via the p38 MAPK signaling pathway.
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The R package limma was used to detect differences in miRNA expression levels between normal and OS samples. The filter criterion was log [fold change (FC)] > 1 and adjusted P-value < 0.05 [35].
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The R package limma was used to detect differences in miRNA expression levels between normal and OS samples. The filter criterion was log [fold change (FC)] > 1 and adjusted P-value < 0.05 [35].
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sections[31] "Availability of data and materials" paragraph 2
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The datasets generated and analyzed during the current study are available in the [GEO DataSets] repository, [https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE65071].
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title
Plasma profiling of miRNAs in human specimens from osteosarcoma patients.
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The R package limma was used to detect differences in miRNA expression levels between normal and OS samples. The filter criterion was log [fold change (FC)] > 1 and adjusted P-value < 0.05 [35].
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E EXPRESSION OMNIBUS (GEO) database. Through real-time quantitative PCR (qRT-PCR), western blotting, colony formatio
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tively regulated tumor growth and metastasis in vivo. Furthermore, rescue assays verified that mi
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Complete file
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Accumulating evidence has revealed that microRNAs (miRNAs) play a crucial role in the progression of OS. In this study, we found that miR-744-5p was the least expressed miRNA in patients with OS by analyzing GSE65071 from the GENE EXPRESSION OMNIBUS (GEO) database. Through real-time quantitative PCR (qRT-PCR), western blotting, colony formation assay, 5-Ethynyl-2-Deoxyuridine (EdU) incorporation assay, transwell migration, and invasion assays, we demonstrated its ability to inhibit the proliferation, migration, and invasion of OS cells in vitro. According to the luciferase reporter assay, transforming growth factor-β1 (TGFB1) was negatively regulated by miR-744-5p and reversed the effects of miR-744-5p on OS. Subcutaneous tumor-forming animal models and tail vein injection lung metastatic models were used in animal experiments, and it was found that miR-744-5p negatively regulated tumor growth and metastasis in vivo. 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