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MicroRNA-135b Regulates Leucine Zipper Tumor Suppressor 1 in Cutaneous Squamous Cell Carcinoma
Edit B Olasz1, Lauren N Seline1, Ashley M Schock1
1Department of Dermatology, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America.
Abstract:
Cutaneous squamous cell carcinoma (cSCC) is the second most common skin malignancy and it presents a therapeutic challenge in organ transplant recipient patients. Despite the need, there are only a few targeted drug treatment options. Recent studies have revealed a pivotal role played by microRNAs (miRNAs) in multiple cancers, but only a few studies tested their function in cSCC. Here, we analyzed differential expression of 88 cancer related miRNAs in 43 study participants with cSCC; 32 immunocompetent, 11 OTR patients, and 15 non-lesional skin samples by microarray analysis. Of the examined miRNAs, miR-135b was the most upregulated (13.3-fold, 21.5-fold; p=0.0001) in both patient groups. Similarly, the miR-135b expression was also upregulated in three cSCC cell lines when evaluated by quantitative real-time PCR. In functional studies, inhibition of miR-135b by specific anti-miR oligonucleotides resulted in upregulation of its target gene LZTS1 mRNA and protein levels and led to decreased cell motility and invasion of both primary and metastatic cSCC cell lines. In contrast, miR-135b overexpression by synthetic miR-135b mimic induced further down-regulation of LZTS1 mRNA in vitro and increased cancer cell motility and invasiveness. Immunohistochemical evaluation of 67 cSCC tumor tissues demonstrated that miR-135b expression inversely correlated with LZTS1 staining intensity and the tumor grade. These results indicate that miR-135b functions as an oncogene in cSCC and provide new understanding into its pathological role in cSCC progression and invasiveness.
Insights
MicroRNA-135b (miR-135b) acts as an oncogene in cutaneous squamous cell carcinoma (cSCC). Inhibiting miR-135b reduced cancer cell invasion, while its overexpression increased invasiveness, highlighting its role in cSCC progression.
Area of Science:
- Oncology
- Molecular Biology
- Dermatology
Background:
- Cutaneous squamous cell carcinoma (cSCC) is a common skin cancer with limited targeted therapies, especially in organ transplant recipients.
- MicroRNAs (miRNAs) are increasingly recognized for their roles in cancer, but their specific functions in cSCC require further investigation.
Purpose of the Study:
- To analyze the differential expression of cancer-related miRNAs in cSCC patients, including organ transplant recipients (OTR).
- To investigate the functional role of miR-135b in cSCC cell behavior and its correlation with tumor characteristics.
Main Methods:
- Microarray analysis of 88 cancer-related miRNAs in 43 cSCC samples (32 immunocompetent, 11 OTR) and 15 non-lesional skin samples.
- Quantitative real-time PCR and functional assays (inhibition/overexpression of miR-135b) in cSCC cell lines.
- Immunohistochemical evaluation of miR-135b and its target LZTS1 in 67 cSCC tumor tissues.
Main Results:
- miR-135b was significantly upregulated in cSCC tissues from both immunocompetent and OTR patients.
- Inhibition of miR-135b decreased cSCC cell motility and invasion by upregulating its target LZTS1.
- Overexpression of miR-135b increased cSCC cell motility and invasion, correlating inversely with LZTS1 expression and tumor grade.
Conclusions:
- miR-135b acts as an oncogene in cSCC, promoting tumor progression and invasiveness.
- Targeting miR-135b may offer a novel therapeutic strategy for cSCC, particularly in high-risk populations like OTR.
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