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Published on: March 17, 2020
MiR-1193 was sponged by LINC00963 and inhibited cutaneous squamous cell carcinoma progression by targeting SOX4
Jingwen Wang1, Chao Li2, Lifa Xu3
1Department of Dermatology, the Second Affiliated Hospital, Anhui Medical University, Hefei, Anhui, 230601, China.
Abstract:
Cutaneous squamous cell carcinoma (CSCC), a class of skin tumor derived from epidermal keratinocyte, is reputed as one of the most malignant tumors globally. MicroRNAs (miRNAs) are increasingly identified as essential players in CSCC. Current study aimed to uncover the impact and mechanism of miR-1193 in CSCC. We identified the low expression of miR-1193 in CSCC cell lines. Gain- and loss-of-function assays showed that miR-1193 acted as an inhibitor of proliferation and migration in CSCC cells. Furthermore, we illustrated that miR-1193 targeted and inhibited SRY-box 4 (SOX4), and that long intergenic non-protein coding RNA 963 (LINC00963) sponged miR-1193 to upregulate SOX4 expression. Rescue assays showed that LINC00963 regulated CSCC progression through miR-1193/SOX4 axis. In conclusion, our study firstly revealed the LINC00963/miR-1193/SOX4 axis in CSCC, indicating miR-1193 as a promising biological target in CSCC progression.
Insights
MicroRNA-1193 (miR-1193) inhibits the growth and spread of cutaneous squamous cell carcinoma (CSCC). This study reveals the LINC00963/miR-1193/SOX4 pathway, highlighting miR-1193 as a potential therapeutic target for CSCC.
Area of Science:
- Oncology
- Molecular Biology
- Dermatology
Background:
- Cutaneous squamous cell carcinoma (CSCC) is a globally significant and aggressive skin cancer.
- MicroRNAs (miRNAs) play crucial roles in the development and progression of CSCC.
- Understanding the specific roles of miRNAs in CSCC is vital for developing targeted therapies.
Purpose of the Study:
- To investigate the role and underlying mechanism of microRNA-1193 (miR-1193) in cutaneous squamous cell carcinoma (CSCC).
- To elucidate the regulatory axis involving long intergenic non-protein coding RNA 963 (LINC00963), miR-1193, and SRY-box 4 (SOX4) in CSCC.
Main Methods:
- Quantitative assessment of miR-1193 expression in CSCC cell lines.
- In vitro gain- and loss-of-function experiments to evaluate miR-1193's impact on CSCC cell proliferation and migration.
- Identification of miR-1193 targets and investigation of LINC00963's role as a miRNA sponge.
- Rescue assays to confirm the functional significance of the LINC00963/miR-1193/SOX4 axis.
Main Results:
- miR-1193 expression was found to be downregulated in CSCC cell lines.
- Overexpression of miR-1193 suppressed CSCC cell proliferation and migration, while its inhibition promoted these processes.
- miR-1193 directly targets and inhibits the expression of SRY-box 4 (SOX4).
- LINC00963 acts as a molecular sponge for miR-1193, leading to increased SOX4 expression and promoting CSCC progression.
Conclusions:
- The study identified and characterized the LINC00963/miR-1193/SOX4 regulatory axis in CSCC.
- miR-1193 functions as a tumor suppressor by inhibiting CSCC cell proliferation and migration via the miR-1193/SOX4 pathway.
- This axis represents a novel mechanism in CSCC pathogenesis and suggests miR-1193 as a potential therapeutic target for managing CSCC.
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