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pmid:33108067

LINC01128 regulates the development of osteosarcoma by sponging miR-299-3p to mediate MMP2 expression and activating Wnt/β-catenin signalling pathway.

Qiang Yao · Ting Chen

Journal of cellular and molecular medicine · 2020 doi:10.1111/jcmm.16046

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complete

Experiment

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Data

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pmid:33108067
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title
LINC01128 regulates the development of osteosarcoma by sponging miR-299-3p to mediate MMP2 expression and activating Wnt/β-catenin signalling pathway.
doi
10.1111/jcmm.16046
pmid
33108067
authors array · 2 items
[0]
Qiang Yao
[1]
Ting Chen
journal
Journal of cellular and molecular medicine
year
2020
abstract
Osteosarcoma (OS) is one of the most common metastatic bone cancers, which results in significant morbidity and mortality. The important role of long non-coding RNAs (lncRNAs) in the biological processes of OS has been demonstrated through several studies. In the current study, we evaluated the role of the lncRNA, LINC01128, in OS. We analysed the expression of LINC01128 in three OS gene expression omnibus (GEO) data sets GSE21257, GSE36001 and GSE42352. The expression of LINC01128 in OS tissues and matched non-tumour tissues obtained from 50 OS patients was detected using qRT-PCR. The association between LINC01128 expression and overall survival of OS patients was evaluated using the Kaplan-Meier method. The effects of LINC01128 knockdown and overexpression were evaluated through in vitro and in vivo assays. The LINC01128/miR-299-3p/ MMP2 axis was verified using dual-luciferase reporter assay and qRT-PCR assays. GEO data sets analysis revealed that the expression of LINC01128 was increased in OS. Elevated LINC01128 expression was accompanied by shorter overall survival in OS patients. Functional studies revealed that LINC01128 knockdown reduced the proliferation, migration and invasion of OS cells both in vitro and in vivo. Mechanistically, LINC01128 sponged miR-299-3p to increase MMP2 expression. Rescue assays determined the role of the LINC01128/miR-299-3p/MMP2 axis in the proliferation, migration and invasion of OS cells. Additionally, the Wnt/β-catenin signalling pathway was activated by LINC01128 and MMP2 in OS cell lines. In summary, this study demonstrates that LINC01128 facilitates OS by functioning as a sponge of miR-299-3p, thus promoting MMP2 expression and activating the Wnt/β-catenin signalling pathway.
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Additionally, the log‐rank test and Kaplan‐Meier method were used to evaluate the overall survival.
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Genome-wide gene expression profiling on pre-chemotherapy biopsies of osteosarcoma patients who developed metastases within 5yrs (n=34) and patients who did not develop metastases within 5yrs (n=19)
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Association of LINC01128 expression with clinicopathological features of osteosarcoma
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LINC01128 level is increased in OS and associated with poor prognosis in OS patients
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Association of LINC01128 expression with clinicopathological features of osteosarcoma
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aplan-Meier method. The effects of LINC01128 knockdown and overexpression were evaluated through in
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. Functional studies revealed that LINC01128 knockdown reduced the proliferation, migration and inv
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pression were evaluated through in vitro and in vivo assays. The LINC01128/miR-299-3p/ MMP2 axis
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n and invasion of OS cells both in vitro and in vivo. Mechanistically, LINC01128 sponged miR-299-
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n, Grand Island, NY, USA). All four human OS cell lines were maintained in a humidified incubator at 37°C with a 5%
[1]
cubator at 37°C with a 5% CO2. The hFOB 1.19 cell line was maintained at 33.5°C with a 5% CO2. Statistical analysi
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line hFOB1.19. MG63, HOS and U2OS cells were cultured in alpha minimal essential medium (α‐MEM; HyClo
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Gibco, Carlsbad, CA, USA). Saos2 cells were cultured in Rosewell Park Memorial Institute 1640 (RPMI‐
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Complete file
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The important role of long non-coding RNAs (lncRNAs) in the biological processes of OS has been demonstrated through several studies. In the current study, we evaluated the role of the lncRNA, LINC01128, in OS. We analysed the expression of LINC01128 in three OS gene expression omnibus (GEO) data sets GSE21257, GSE36001 and GSE42352. The expression of LINC01128 in OS tissues and matched non-tumour tissues obtained from 50 OS patients was detected using qRT-PCR. The association between LINC01128 expression and overall survival of OS patients was evaluated using the Kaplan-Meier method. The effects of LINC01128 knockdown and overexpression were evaluated through in vitro and in vivo assays. The LINC01128/miR-299-3p/ MMP2 axis was verified using dual-luciferase reporter assay and qRT-PCR assays. GEO data sets analysis revealed that the expression of LINC01128 was increased in OS. Elevated LINC01128 expression was accompanied by shorter overall survival in OS patients. Functional studies revealed that LINC01128 knockdown reduced the proliferation, migration and invasion of OS cells both in vitro and in vivo. Mechanistically, LINC01128 sponged miR-299-3p to increase MMP2 expression. Rescue assays determined the role of the LINC01128/miR-299-3p/MMP2 axis in the proliferation, migration and invasion of OS cells. Additionally, the Wnt/β-catenin signalling pathway was activated by LINC01128 and MMP2 in OS cell lines. 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