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Updated: Mar 28, 2026

Three-Dimensional 3D Tumor Spheroid Invasion Assay
Published on: May 1, 2015
Rab23 promotes squamous cell carcinoma cell migration and invasion via integrin β1/Rac1 pathway
Qiang Jian1, Ye Miao1, Li Tang1
1Department of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi Province, China.
Abstract:
Rab23 was a member of Ras-related small GTPase family, which played a key role in the regulation of Shh signaling pathway. However, the function and regulatory mechanism of Rab23 in cutaneous squamous cell carcinoma was unknown. In this study, we found that the expression level of Rab23 was higher in moderately to poorly tumor differentiation tissue and non-exposed positions, and no statistically significant difference showed in Rab23 expression according to trauma/chronic disease, location on lips/ears, tumor size, gender, or age. Interestingly, we found that Rab23 RNAi suppressed cell invasion and Rab23 overexpression promoted cell invasion depended on GTP-bound form of Rab23. Inhibition of Rac1 activity or Rac1 silencing with siRNA fragment attenuated Rab23 promoted cells migration and invasion. Notably, we confirmed that Rab23 was co-localized with integrin β1 in cell membrane of Rab23 WT and Rab23 Q68L stable expression cells and Rab23 efficiently coprecipitated with integrin β1 and Tiam1 in a GTP-dependent manner. Further, integrin β1 siRNA interrupted the coprecipitation between Rab23 and Tiam1 and attenuated Rab23 promoted cells migration and invasion. Taken together, our results indicated that Rab23 promotes squamous cell carcinoma cells migration and invasion by regulating Integrin β1/Tiam1/Rac1 pathway.
Insights
Rab23 promotes skin cancer invasion by activating the Integrin β1/Tiam1/Rac1 pathway. This Ras-related small GTPase is upregulated in poorly differentiated tumors, suggesting a role in cancer progression.
Area of Science:
- Oncology
- Cell Biology
- Molecular Biology
Background:
- Rab23, a Ras-related small GTPase, regulates the Shh signaling pathway.
- The role of Rab23 in cutaneous squamous cell carcinoma (cSCC) remains unclear.
Purpose of the Study:
- To investigate the function and regulatory mechanisms of Rab23 in cSCC.
- To elucidate the molecular pathways involved in Rab23-mediated cSCC progression.
Main Methods:
- Quantitative analysis of Rab23 expression in cSCC tissues.
- RNA interference (RNAi) and overexpression studies to assess Rab23's effect on cell invasion.
- Co-immunoprecipitation and immunofluorescence to study protein interactions.
- Rac1 inhibition and silencing experiments.
Main Results:
- Rab23 expression is higher in poorly differentiated cSCC and non-exposed tumor sites.
- Rab23 promotes cSCC cell migration and invasion in a GTP-dependent manner.
- Rab23 interacts with Integrin β1 and Tiam1, regulating the Tiam1/Rac1 pathway.
Conclusions:
- Rab23 drives cSCC cell invasion and migration.
- The Integrin β1/Tiam1/Rac1 pathway is a key mechanism by which Rab23 promotes cSCC progression.
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