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Tissue Engineering of Tumor Stromal Microenvironment with Application to Cancer Cell Invasion
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Proteasome Subunit Alpha Type-7 Expression Suppresses Cutaneous Squamous Cell Carcinoma Progression by Inhibiting
Xiangshu Xu1,2, Meiling Pei2, Ki-Yeol Kim3
1Department Dermatology, Yanbian University Hospital, Yanji, P.R. China.
In Vivo (Athens, Greece)
|June 27, 2023
Summary
Proteasome subunit alpha type-7 (PSMA7) may act as a tumor suppressor in cutaneous squamous cell carcinoma (cSCC). PSMA7 down-regulation increased cancer-associated cytokines, suggesting an antitumoral role in cSCC pathogenesis.
Area of Science:
- Oncology
- Molecular Biology
- Immunology
Background:
- Cutaneous squamous cell carcinoma (cSCC) is a prevalent non-melanoma skin cancer with increasing incidence.
- The role of Proteasome subunit alpha type-7 (PSMA7) in cancer pathogenesis, including cSCC, is debated.
- This study investigates the specific functions of PSMA7 in the development of cSCC.
Purpose of the Study:
- To elucidate the role of PSMA7 in the pathogenesis of cutaneous squamous cell carcinoma (cSCC).
- To determine the relationship between PSMA7 expression and clinicopathological features and patient survival in cSCC.
- To investigate the in vitro effects of PSMA7 modulation on cSCC cell behavior and cytokine expression.
Main Methods:
- Clinicopathological characteristics of 131 cSCC patients were analyzed.
- Immunohistochemical staining assessed PSMA7, NOD1, and MAVS expression in cSCC tissues.
- In vitro experiments evaluated the impact of PSMA7 down-regulation on cSCC cell viability, invasiveness, and cytokine mRNA expression.
Main Results:
- High PSMA7 expression correlated with favorable recurrence-free survival and lower histologic grade in cSCC patients.
- PSMA7 expression was negatively correlated with NOD1 and MAVS expression in cSCC tissues.
- PSMA7 down-regulation in vitro reduced cSCC cell viability and invasiveness while increasing pro-inflammatory cytokine mRNA levels (TNF-α, IL-1α, IL-6, IL-8).
Conclusions:
- PSMA7 exhibits antitumoral functions in cSCC, potentially through the degradation of NOD1 and MAVS.
- This degradation may lead to the suppression of a cancer-associated cytokine network.
- PSMA7's role as a tumor suppressor in cSCC warrants further investigation for therapeutic strategies.
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