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Updated: Oct 6, 2025

Author Spotlight: RNA FISH for Locating lncRNA-SNHG6 in Osteosarcoma Cells
Published on: June 16, 2023
Silencing long non-coding RNA LINC00960 inhibits osteosarcoma proliferation by sponging miR-107 to downregulate SALL4
Yubo Shi1, Bo Yang1, Yingchun Zhao1
1Department of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Abstract:
long non-coding RNAs (lncRNAs), as tumor suppressors or oncogenes, have been identified to play key roles in tumorigenesis. The present study explored the roles and potential mechanisms of LINC00960 in osteosarcoma (OS). In vitro study showed that silencing LINC00960 inhibited proliferation, migration and invasion of 143B and MG63. In vivo study demonstrated that knockdown of LINC00960 repressed tumor growth. Further investigation revealed that LINC00960 could regulate SALL4 by sponging miR-107 to promote the progression of OS. Together, LINC00960 is a tumor oncogene in the development and prognosis of OS, which may be a new therapeutic target for OS.
Insights
Long non-coding RNA LINC00960 acts as an oncogene in osteosarcoma (OS) by promoting cell proliferation and tumor growth. It regulates SALL4 via sponging miR-107, suggesting LINC00960 as a potential therapeutic target for OS.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- Long non-coding RNAs (lncRNAs) are implicated in tumorigenesis, acting as either tumor suppressors or oncogenes.
- Osteosarcoma (OS) is a primary bone malignancy with significant impact on patient prognosis.
Purpose of the Study:
- To investigate the role and underlying mechanisms of LINC00960 in osteosarcoma progression.
- To determine the potential of LINC00960 as a therapeutic target for OS.
Main Methods:
- In vitro studies involving cell proliferation, migration, and invasion assays in OS cell lines (143B and MG63) with LINC00960 silencing.
- In vivo studies using xenograft models to assess the effect of LINC00960 knockdown on tumor growth.
- Mechanistic studies exploring the interaction between LINC00960, miR-107, and SALL4.
Main Results:
- Silencing LINC00960 significantly inhibited proliferation, migration, and invasion of osteosarcoma cells in vitro.
- Knockdown of LINC00960 repressed tumor growth in vivo.
- LINC00960 was found to regulate SALL4 expression by sponging miR-107, thereby promoting OS progression.
Conclusions:
- LINC00960 functions as an oncogene in the development and prognosis of osteosarcoma.
- Targeting LINC00960 presents a potential novel therapeutic strategy for osteosarcoma treatment.
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