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Author Spotlight: A Selective Luciferase-Based Assay for Monitoring ATG4B 27 Activity in Cells
Published on: June 30, 2023
High-throughput screening and clinical importance of autophagy-associated genes in basal cell carcinoma
Saffet Ulutas1, Mehmet Mutaf1, Mustafa Nihat Koc1
1Department of Plastic and Reconstructive Surgery, Faculty of Medicine, Gaziantep University, Gaziantep, Turkey.
Abstract:
Autophagy is a type II programmed cell death mechanism that plays a critical role in preserving cellular homeostasis through the regulation of protein, lipid, and organelle quality control. It has become gradually evident that autophagy plays a fundamental role in the initiation and progression of various types of human cancers. Nevertheless, its significance in non-melanoma skin cancers, particularly in basal cell carcinoma, has not been well documented and remains largely elusive. In this study, we aimed to illuminate the role of autophagy-associated signaling signatures during development and progression of basal cell carcinoma. For the study, a total of 72 autophagy-related genes were screened using a high-throughput qPCR approach integrating Fluidigm 96.96 Dynamic Array™ integrated fluidic circuits (IFC) and BioMark™ HD Real-Time PCR system, which enabled efficient and precise analysis of gene expression patterns. Results were analyzed using Fluidigm's Real-Time PCR Analysis software and 2-ΔΔCt formula was used for the calculation of expression changes. Notably, expression levels of INS, TMEM74 and IFNA2 genes were identified to be prominently altered in BCC comparted to adjacent healthy tissues. However, only IFNA2 expression showed statistically significant change in BCC. Consequently, these findings suggest that IFNA2 might play significant role in the regulation of autophagy in BCC development and progression and can be therapeutically targeted.
Insights
Autophagy is crucial for cell health and cancer. This study found Interferon Alpha 2 (IFNA2) gene expression significantly changes in basal cell carcinoma, suggesting its role in cancer development and potential therapeutic targeting.
Area of Science:
- Cellular biology
- Molecular oncology
- Dermatology
Background:
- Autophagy is a key cellular process for maintaining homeostasis and is implicated in various cancers.
- The role of autophagy in non-melanoma skin cancers, specifically basal cell carcinoma (BCC), is not well understood.
- Understanding autophagy's role in BCC is crucial for developing targeted therapies.
Purpose of the Study:
- To investigate the role of autophagy-associated signaling in basal cell carcinoma (BCC) development and progression.
- To identify specific autophagy-related genes altered in BCC.
- To explore the potential of these genes as therapeutic targets.
Main Methods:
- Screening of 72 autophagy-related genes using high-throughput quantitative PCR (qPCR).
- Utilized Fluidigm 96.96 Dynamic Array™ integrated fluidic circuits (IFC) and BioMark™ HD Real-Time PCR system for gene expression analysis.
- Statistical analysis of gene expression data using Fluidigm's Real-Time PCR Analysis software and the 2-ΔΔCt method.
Main Results:
- Expression levels of INS, TMEM74, and IFNA2 genes were altered in BCC compared to healthy tissues.
- Interferon Alpha 2 (IFNA2) gene expression showed a statistically significant change in BCC.
- These findings highlight potential alterations in autophagy signaling pathways within BCC.
Conclusions:
- IFNA2 may play a significant role in the regulation of autophagy during BCC development and progression.
- IFNA2 represents a potential therapeutic target for basal cell carcinoma.
- Further research into IFNA2's function in BCC is warranted.
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