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Published on: July 24, 2014
Overexpression of ROCK1 and ROCK2 inhibits human laryngeal squamous cell carcinoma
Junbo Zhang1, Xue He2, Yueying Ma3
1Department of Otolaryngology, Head and Neck Surgery, Peking University First Hospital Beijing 100034, China.
Abstract:
Rho-associated coiled-coil containing protein kinase (ROCK) over-expression has been implicated in the progression of many tumor types. The aim of this study was to explore the roles of ROCK1 and ROCK2 in human laryngeal squamous cell carcinoma (LSCC). ROCK1 and ROCK2 expression levels were examined in 50 cases of human LSCC samples by immunohistochemistry. Effects of ROCK1 and ROCK2 on LSCC cell proliferation and motility were investigated in the presence of the ROCK inhibitor Y-27632. The results showed that ROCK1 expression was positively correlated with tumor size and lymph node metastasis (P < 0.05); ROCK2 positively correlated with tumor size (P < 0.05). Inhibition of ROCK1 and ROCK2 by Y-27632 significantly inhibits proliferation, migration, and invasion of LSCC cells. Our data indicate that expression of ROCK1 and ROCK2 are closely associated with tumor growth and lymph node metastasis of LSCC. Thus, these two ROCK isoforms may be useful as molecular makers for LSCC diagnosis and may be useful therapeutic targets as well.
Insights
Rho-associated coiled-coil containing protein kinase (ROCK) 1 and 2 are overexpressed in laryngeal cancer, correlating with tumor size and metastasis. Inhibiting ROCK1/2 with Y-27632 suppressed cancer cell growth and invasion.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- Rho-associated coiled-coil containing protein kinase (ROCK) signaling pathways are implicated in various cancers.
- ROCK1 and ROCK2 are key isoforms involved in cellular processes like proliferation, migration, and invasion.
Purpose of the Study:
- To investigate the expression and roles of ROCK1 and ROCK2 in human laryngeal squamous cell carcinoma (LSCC).
- To determine the correlation between ROCK1/ROCK2 expression and clinicopathological features of LSCC.
- To evaluate the therapeutic potential of ROCK inhibition in LSCC.
Main Methods:
- Immunohistochemistry was used to assess ROCK1 and ROCK2 expression in 50 human LSCC samples.
- LSCC cell lines were treated with the ROCK inhibitor Y-27632 to study the effects on proliferation, migration, and invasion.
Main Results:
- ROCK1 expression positively correlated with tumor size and lymph node metastasis in LSCC.
- ROCK2 expression positively correlated with tumor size in LSCC.
- Inhibition of ROCK1 and ROCK2 by Y-27632 significantly reduced LSCC cell proliferation, migration, and invasion.
Conclusions:
- ROCK1 and ROCK2 expression are closely associated with tumor growth and lymph node metastasis in LSCC.
- ROCK1 and ROCK2 may serve as valuable molecular markers for LSCC diagnosis.
- Targeting ROCK isoforms presents a potential therapeutic strategy for LSCC.
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