Related Experiment Video
Updated: Jun 21, 2026

A Preclinical Mouse Model of Osteosarcoma to Define the Extracellular Vesicle-mediated Communication Between Tumor and Mesenchymal Stem Cells
Published on: May 6, 2018
Functional elucidation of MiR-34 in osteosarcoma cells and primary tumor samples
Chunlei He1, Jianyi Xiong, Xiaoping Xu
1Guangzhou Medical College, Guangdong Province, China.
Abstract:
MiR-34s have been characterized as direct p53 targets, which induce apoptosis, cell cycle arrest, and senescence. MiR-34s were found to associate with tumorigenesis. Thus far, there is no study on the role of MiR-34s in osteosarcoma. In the current study, we intensively investigated the function of MiR-34s in two osteosarcoma cell lines: U2OS (p53(+/+)) and SAOS-2 (p53(-/-)). We found that MiR-34s affect the expression of its target genes partially in a p53-dependent manner. And p53 also partially contributes to the MiR-34s induced cell cycle arrest and apoptosis. Finally, we examined the expression, genetic and epigenetic alterations of MiR-34 gene in 117 primary osteosarcoma samples. Expression of MiR-34s was decreased in tumor samples, and MiR-34 genes underwent minimal deletions and epigenetic inactivation in osteosarcomas.
Insights
MicroRNAs (MiR-34s) are linked to cancer and impact cell death and growth. This study reveals MiR-34s are downregulated in osteosarcoma, partly due to p53 interactions.
Area of Science:
- Molecular Biology
- Genetics
- Oncology
Background:
- MicroRNAs (MiR-34s) are known p53 targets involved in apoptosis, cell cycle arrest, and senescence.
- MiR-34s are implicated in tumorigenesis, but their role in osteosarcoma remains uninvestigated.
Purpose of the Study:
- To investigate the function of MiR-34s in osteosarcoma.
- To explore the relationship between MiR-34s, p53, and osteosarcoma progression.
Main Methods:
- Functional analysis of MiR-34s in p53 wild-type (U2OS) and p53-null (SAOS-2) osteosarcoma cell lines.
- Assessment of MiR-34 gene expression, genetic alterations (deletions), and epigenetic modifications in 117 primary osteosarcoma samples.
Main Results:
- MiR-34s influenced target gene expression in a manner partially dependent on p53.
- p53 partially mediated MiR-34s-induced cell cycle arrest and apoptosis.
- MiR-34 expression was significantly decreased in osteosarcoma tissues.
- MiR-34 genes showed minimal deletions but underwent epigenetic inactivation in osteosarcomas.
Conclusions:
- MiR-34s play a role in osteosarcoma, with their function partially regulated by p53.
- Downregulation of MiR-34s in osteosarcoma is associated with genetic and epigenetic alterations, suggesting a tumor-suppressive role.
More Related Videos
08:47Improved Visualization of Lung Metastases at Single Cell Resolution in Mice by Combined In-situ Perfusion of Lung Tissue and X-Gal Staining of lacZ-Tagged Tumor Cells
Published on: August 21, 2012
10:27Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020