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Published on: June 15, 2019
Complement Component C3 and Complement Factor B Promote Growth of Cutaneous Squamous Cell Carcinoma.
Pilvi Riihilä1, Liisa Nissinen1, Mehdi Farshchian1
1Department of Dermatology, University of Turku and Turku University Hospital, Turku, Finland; MediCity Research Laboratory, University of Turku, Turku, Finland.
Complement component C3 and complement factor B (CFB) are upregulated in cutaneous squamous cell carcinoma (cSCC). Targeting C3 and CFB inhibits cSCC growth, migration, and proliferation, suggesting their potential as therapeutic targets for this skin cancer.
Area of Science:
- Oncology
- Immunology
- Dermatology
Background:
- Cutaneous squamous cell carcinoma (cSCC) is a common metastatic skin cancer with rising incidence.
- The roles of complement system proteins, specifically C3 and complement factor B (CFB), in cSCC development are not fully understood.
Purpose of the Study:
- To investigate the expression and function of C3 and CFB in cutaneous squamous cell carcinoma.
- To evaluate C3 and CFB as potential biomarkers and therapeutic targets for cSCC.
Main Methods:
- Quantitative PCR and Western blotting were used to analyze C3 and CFB expression in cSCC cell lines and normal keratinocytes.
- Immunohistochemistry was performed on human cSCC tissues, actinic keratoses, and normal skin.
- Gene knockdown experiments and *in vivo* xenograft models were utilized to assess the functional impact of C3 and CFB.
Main Results:
- C3 and CFB expression were significantly upregulated in cSCC cells compared to normal keratinocytes.
- Higher C3 and CFB labeling was observed in invasive cSCCs and related subtypes compared to early-stage lesions and normal skin.
- Knockdown of C3 and CFB inhibited cSCC cell migration, proliferation, extracellular signal-regulated kinase 1/2 activation, and xenograft tumor growth.
Conclusions:
- C3 and CFB play crucial roles in the development and progression of cutaneous squamous cell carcinoma.
- C3 and CFB represent promising biomarkers and potential therapeutic targets for managing metastatic cSCC.
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