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LINC01278 is Highly Expressed in Osteosarcoma and Participates in the Development of Tumors by Mediating the
Guo-Feng Zhang1, Bai-Sui Zhou1, Xiao-Chun An1
1Department of Orthopedics, Yantai Affiliated Hospital of Binzhou Medical University, Yantai 261400, People's Republic of China.
Purpose:
There is increasing evidence that non-coding RNAs (ncRNAs), including long non-coding RNAs (lncRNAs) and microRNAs (miRNAs), produce a critical regulatory effect on osteosarcoma (OS). LINC01278, as a newly discovered lncRNA, is found to be highly expressed in OS, but its related mechanism remains unclear. This research, therefore, is designed to study the mechanism of LINC01278 in OS and to find potential targets for clinical use.
Methods:
qRT-PCR was applied to determine the relative expression of LINC01278 and analyze its diagnostic value in OS. CCK-8, Transwell and flow cytometry were utilized for the determination of cell proliferation, migration/invasion, and apoptosis. RIP and RNA pull-down experiments were used to verify the targeted binding effect of miR-134-5p and LINC01278. The relationship between miR-134-5p and LINC01278 or KRAS was analyzed using dual luciferase reporter gene. The effects of LINC01278 on tumor growth in nude mice was analyzed by in vivo experiment.
Results:
qRT-PCR showed that LINC01278 increased in OS tissues and serum, indicating poor prognosis. In addition, LINC01278 was also of high value for OS diagnosis. Functional experiments showed that LINC01278 inhibited KRAS-mediated OS cell proliferation and metastasis through miR-134-5p. Finally, the results of an in vivo animal model indicated that LINC01278 promoted OS growth.
Conclusion:
LINC01278 is expressed highly in OS, and patients with high LINC01278 expression have poor prognosis. Moreover, LINC01278 can suppress the proliferation and apoptosis of OS cells through mediating miR-134-5p/KRAS axis, which is expected to become a potential therapeutic target for OS.
Insights
High expression of LINC01278 in osteosarcoma (OS) correlates with poor prognosis and aids diagnosis. This long non-coding RNA suppresses OS cell proliferation and metastasis via the miR-134-5p/KRAS axis, offering a potential therapeutic target.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- Non-coding RNAs (ncRNAs), including long non-coding RNAs (lncRNAs) and microRNAs (miRNAs), play critical regulatory roles in osteosarcoma (OS).
- LINC01278 is a newly identified lncRNA with elevated expression in OS, but its underlying mechanism and clinical significance require elucidation.
Purpose of the Study:
- To investigate the mechanistic role of LINC01278 in osteosarcoma (OS).
- To identify LINC01278 as a potential diagnostic marker and therapeutic target for OS.
Main Methods:
- Quantitative reverse transcription polymerase chain reaction (qRT-PCR) for LINC01278 expression analysis and diagnostic value assessment.
- Cellular assays (CCK-8, Transwell, flow cytometry) to evaluate OS cell proliferation, migration, invasion, and apoptosis.
- RNA immunoprecipitation (RIP), RNA pull-down, and dual luciferase reporter assays to confirm molecular interactions.
- In vivo experiments in nude mice to assess the effect of LINC01278 on tumor growth.
Main Results:
- LINC01278 expression was significantly upregulated in OS tissues and serum, correlating with poor prognosis and demonstrating diagnostic value.
- Functional studies revealed that LINC01278 inhibits OS cell proliferation and metastasis by modulating the miR-134-5p/KRAS axis.
- In vivo studies confirmed that LINC01278 promotes OS tumor growth.
Conclusions:
- Elevated LINC01278 expression in OS is associated with poor patient outcomes and serves as a diagnostic indicator.
- LINC01278 exerts its oncogenic effects by suppressing proliferation and apoptosis through the miR-134-5p/KRAS pathway.
- LINC01278 represents a promising therapeutic target for osteosarcoma treatment.
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