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Updated: Mar 16, 2026

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Published on: January 16, 2026
SRCIN1 Suppressed Osteosarcoma Cell Proliferation and Invasion
Peng Wang1, Hu Wang2, Xiaotao Li3
1Department of Orthopedics, The Fourth Hospital of Harbin Medical University, Harbin, Heilongjiang, 150001, China.
Abstract:
SRCIN1 (SRC kinase signalling inhibitor 1) is a new tumor suppressor gene. Previous studies showed that SRCIN1 played a tumor suppressor role in the development of lung cancer and breast cancer. However, the role of SRCIN1 in osteosarcoma is still unknown. In this study, we demonstrated that SRCIN1 was downregulated in osteosarcoma cell lines compared with osteoblastic cell line. Moreover, SRCIN1 was downregulated in osteosarcoma tissues compared with the adjacent tissues. Further investigation revealed that overexpression of SRCIN1 inhibited the osteosarcoma cell line MG-63 proliferation. This effect was confirmed by measuring the ki-67 and PCNA expression. SRCIN1 overexpression promoted E-cadherin expression and suppressed N-cadherin, Vimentin and Snail expression, suggesting that SRCIN1 overexpression inhibited EMT of the osteosarcoma cell. In addition, ectopic expression of SRCIN1 inhibited the MG-63 cell colony formation and invasion. These data suggested that SRCIN1 acted as a tumor suppressor gene in the development of osteosarcoma.
Insights
SRCIN1 (SRC kinase signalling inhibitor 1) acts as a tumor suppressor in osteosarcoma. Its downregulation correlates with tumor progression, while its overexpression inhibits cancer cell proliferation and metastasis.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- SRCIN1 (SRC kinase signalling inhibitor 1) is recognized as a tumor suppressor gene in lung and breast cancers.
- The specific role of SRCIN1 in osteosarcoma development remains largely unexplored.
Purpose of the Study:
- To investigate the expression levels of SRCIN1 in osteosarcoma.
- To determine the functional role of SRCIN1 in osteosarcoma cell proliferation, epithelial-mesenchymal transition (EMT), colony formation, and invasion.
Main Methods:
- Quantitative analysis of SRCIN1 expression in osteosarcoma cell lines and tissues.
- Overexpression of SRCIN1 in MG-63 osteosarcoma cells.
- Assessment of cell proliferation using Ki-67 and PCNA markers.
- Evaluation of EMT markers (E-cadherin, N-cadherin, Vimentin, Snail).
- Colony formation and invasion assays.
Main Results:
- SRCIN1 expression was significantly downregulated in osteosarcoma cell lines and tissues compared to normal controls.
- Overexpression of SRCIN1 suppressed MG-63 cell proliferation, colony formation, and invasion.
- SRCIN1 overexpression upregulated E-cadherin and downregulated N-cadherin, Vimentin, and Snail, indicating inhibition of EMT.
Conclusions:
- SRCIN1 functions as a tumor suppressor gene in osteosarcoma.
- Downregulation of SRCIN1 is associated with osteosarcoma progression.
- SRCIN1 may serve as a potential therapeutic target for osteosarcoma treatment.
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