Knockdown of Simulated-Solar-Radiation-Sensitive miR-205-5p Does Not Induce Progression of Cutaneous Squamous Cell Carcinoma In Vitro

• Published in: International journal of molecular sciences Vol. 24; no. 22; p. 16428
• Main Authors: Bender, Marc, Chen, I-Peng, Henning, Stefan, Degenhardt, Sarah, Mhamdi-Ghodbani, Mouna, Starzonek, Christin, Volkmer, Beate, Greinert, Rüdiger
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.11.2023
• Subjects: Apoptosis; Cell adhesion & migration; Cell cycle; Cell growth; cSCC cell lines; cutaneous squamous cell carcinoma (cSCC); Development and progression; Gene expression; Genes; Investigations; Medical prognosis; Melanoma; Metastasis; MicroRNA; MicroRNAs; miRNAs; Mutation; Radiation; Reagents; simulated solar radiation (SSR); Skin; Skin cancer; Squamous cell carcinoma; United Kingdom; Germany
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms242216428

Solar radiation is the main risk factor for cSCC development, yet it is unclear whether the progression of cSCC is promoted by solar radiation in the same way as initial tumorigenesis. Additionally, the role of miRNAs, which exert crucial functions in various tumors, needs to be further elucidated in the context of cSCC progression and connection to solar radiation. Thus, we chronically irradiated five cSCC cell lines (Met-1, Met-4, SCC-12, SCC-13, SCL-II) with a custom-built irradiation device mimicking the solar spectrum (UVB, UVA, visible light (VIS), and near-infrared (IRA)). Subsequently, miRNA expression of 51 cancer-associated miRNAs was scrutinized using a flow cytometric multiplex quantification assay (FirePlex®, Abcam). In total, nine miRNAs were differentially expressed in cell-type-specific as well as universal manners. miR-205-5p was the only miRNA downregulated after SSR-irradiation in agreement with previously gathered data in tissue samples. However, inhibition of miR-205-5p with an antagomir did not affect cell cycle, cell growth, apoptosis, or migration in vitro despite transient upregulation of oncogenic target genes after miR-205-5p knockdown. These results render miR-205-5p an unlikely intracellular effector in cSCC progression. Thus, effects on intercellular communication in cSCC or the simultaneous examination of complementary miRNA sets should be investigated.