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Circulating Long Non-Coding RNAs as Novel Potential Biomarkers for Osteogenic Sarcoma.
Sutpirat Moonmuang1, Parunya Chaiyawat1,2, Salinee Jantrapirom3,4
1Center of Multidisciplinary Technology for Advanced Medicine (CMUTEAM), Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Cancers
|August 27, 2021
Summary
This study identifies thirteen circulating long non-coding RNAs (c-lncRNAs) as potential biomarkers for osteosarcoma (OS) detection. These novel biomarkers could aid in non-invasive cancer diagnosis and precision medicine for OS management.
Area of Science:
- Oncology
- Molecular Biology
- Biomarker Discovery
Background:
- Circulating cell-free nucleic acids are promising for non-invasive cancer diagnostics.
- Non-coding RNAs (ncRNAs) are implicated in tumor pathogenesis and show potential as cancer biomarkers.
- The utility of circulating long ncRNAs (c-lncRNAs) in osteosarcoma (OS) remains largely unexplored.
Purpose of the Study:
- To systematically review and identify c-lncRNAs associated with osteosarcoma.
- To explore the potential of these c-lncRNAs as diagnostic biomarkers for OS.
- To discuss the clinical implications of c-lncRNAs in OS management and precision oncology.
Main Methods:
- Systematic literature review to identify relevant studies.
- Analysis of circulating long non-coding RNAs (c-lncRNAs) expression in osteosarcoma patients.
- Evaluation of the association between c-lncRNA expression patterns and OS.
Main Results:
- Thirteen specific c-lncRNAs were identified with altered expression in the blood of OS patients.
- These c-lncRNAs demonstrate potential as novel biomarkers for osteosarcoma.
- The findings suggest distinct expression patterns linked to OS pathogenesis.
Conclusions:
- Circulating long non-coding RNAs represent a promising avenue for non-invasive osteosarcoma detection.
- The identified c-lncRNAs may contribute to improved clinical decision-making in OS management.
- This research provides insights for developing future precision medicine strategies in osteosarcoma oncology.

