Differential Expression of Galectin-3, Caspase-1, and Phosphorylated P53: Diagnostic Biomarkers for Basal Cell Carcinoma: A Case-Control Study.

阅读:2
作者:Niamoradi Mahsa, Babajani Fatemeh, Roghani Seyed Askar, Goodarzi Mohammad Taghi, Asadi Soheila
BACKGROUND AND AIMS: Basal cell carcinoma (BCC) is a common form of skin cancer. By considering the role of Galectin-3 (Gal-3), Caspase-1, and Phosphorylated p53 (pP53), they might have an essential role in BCC development. This study aimed to examine the genes and their corresponding proteins in the tumor tissue of patients with BCC and compare them to those in the tumor margins. Furthermore, their potential roles as biomarkers were evaluated. MATERIALS AND METHODS: The gene expression of Gal-3 and Caspase-1 in 25 tumor tissues and 25 tumor margin tissues of BCC subjects was analyzed by Real-Time PCR. The western blot was applied to assess Gal-3, Caspase-1, and pP53; moreover, receiver operating characteristic (ROC) curve analysis was utilized for the determination of these genes' RNA levels as potential biomarkers. RESULTS: Our findings indicated the increased Gal-3 and Caspase-1 gene expression in tumor tissues, compared to the tumor margin tissue in BCC. Gal-3, Caspase-1, and pP53 protein expression in tumor tissues had a significant elevation, compared to tumor margin tissue samples. The result of ROC analysis showed that the AUC for Gal-3 and Caspase-1 were 0.803 (sensitivity: 95%, specificity: 65%, p = 0.001) and 0.812 (sensitivity: 95%, specificity: 70%, p < 0.001), respectively. CONCLUSION: The upregulation of Gal-3 and Caspase-1 and downregulation of P53 suggest these genes and proteins play a crucial role in the tumor microenvironment, and based on our findings, they can be considered potential biomarkers. Additionally, these genes and proteins may be regarded as therapeutic targets based on future functional studies.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。