Related Experiment Video
Updated: Aug 19, 2026

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma
Published on: April 12, 2019
Overexpression of the sis oncogene in a canine osteosarcoma cell line
1Department of Molecular Medicine, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA. ral1@cornell.edu
Abstract:
Specific oncogenes that contribute to the pathogenesis of canine osteosarcoma (OS) have not been identified. In the process of characterizing four OS cell lines, we have found one cell line, CO8, that overexpresses the sis oncogene, which encodes the platelet-derived growth factor (PDGF)-beta. The expression of an important downstream transcriptional target of the PDGF signaling pathway, c-myc, is also elevated fourfold. Conditioned medium from CO8 alone specifically induces tyrosine phosphorylation and therefore the activation of the PDGF-alpha and PDGF-beta receptors on murine 3T3 cells. All of the canine OS lines tested contain PDGF receptors and therefore are capable of responding to PDGE Given the importance of PDGF in promoting cell proliferation, migration, and cell survival, the activation of the sis oncogene and the resultant growth factor autocrine loop potentially contribute to the pathogenesis of a subset of canine osteosarcomas.
Insights
Researchers identified the sis oncogene in canine osteosarcoma cell lines, suggesting a role for platelet-derived growth factor (PDGF) in tumor development. This discovery may lead to new therapeutic strategies for canine osteosarcoma.
Area of Science:
- Oncology
- Molecular Biology
- Canine Cancer Research
Background:
- Specific oncogenes driving canine osteosarcoma (OS) pathogenesis remain unidentified.
- Understanding the molecular mechanisms of OS is crucial for developing targeted therapies.
Purpose of the Study:
- To identify specific oncogenes involved in canine osteosarcoma.
- To investigate the role of platelet-derived growth factor (PDGF) signaling in canine OS.
Main Methods:
- Characterization of four canine osteosarcoma cell lines.
- Analysis of sis oncogene and c-myc expression levels.
- Assessment of PDGF receptor activation in response to conditioned medium.
Main Results:
- One cell line (CO8) overexpressed the sis oncogene, encoding PDGF-beta.
- Elevated expression of c-myc, a downstream target of PDGF signaling, was observed.
- Conditioned medium from CO8 induced PDGF receptor activation in murine 3T3 cells, indicating functional PDGF signaling.
Conclusions:
- The sis oncogene and subsequent PDGF autocrine loop may contribute to the pathogenesis of a subset of canine osteosarcomas.
- Canine osteosarcoma cell lines possess functional PDGF receptors, making them responsive to PDGF.
- This finding opens avenues for exploring PDGF-targeted therapies in canine osteosarcoma.
Related Concept Videos
Abnormal Proliferation
Cancer-Critical Genes I: Proto-oncogenes
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
Rous Sarcoma Virus (RSV) and Cancer
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...

