ZC3H15 Correlates with a Poor Prognosis and Tumor Progression in Melanoma

Author:

Li Qian12,Hou Jianbing23,Guo Chengda4,Zhang Yanli1,Liu Lichao1,Hu Huanrong1,Shi Shaomin15,Ji Yacong1,Guo Leiyang1,Shi Yaqiong1,Liu Yaling1ORCID,Cui Hongjuan23ORCID

Affiliation:

1. Department of Dermatology, The Third Hospital of Hebei Medical University, No. 139, Ziqiang Road, Shijiazhuang, 050051 Hebei, China

2. State Key Laboratory of Silkworm Genome Biology, Southwest University, No. 2, Tiansheng Road, Beibei District, Chongqing 400715, China

3. Cancer Center, Medical Research Institute, Southwest University, No. 2, Tiansheng Road, Beibei District, Chongqing 400715, China

4. Department of Cardiology, The Third Hospital of Hebei Medical University, Shijiazhuang, 050051 Hebei, China

5. Department of Dermatology, The Fifth Hospital of Shijiazhuang, Shijiazhuang, 050051 Hebei, China

Abstract

Zinc figure CCCH-type containing 15 (ZC3H15), also called developmentally regulated GTP-binding protein 1 (DRG1) family regulatory protein 1 (DFRP1), is a zinc finger containing protein. Despite playing a role in cellular signaling, it is found overexpressed in acute myeloid leukemia and also an independent prognostic marker in hepatocellular carcinoma patients. However, the biological effect of ZC3H15 in malignant melanoma (MM) remains unexplored. The expression of ZC3H15 in patients was analyzed using the R2: Genomics Analysis and Visualization Platform database. Immunohistochemical analysis, western blot, and qRT-PCR were used to detect ZC3H15 expression in melanoma tissues and cell lines. MTT, BrdU, flow cytometry assay, transwell, and western blot were performed to explore the proliferation, cell cycle, invasion, and migration of melanoma cells. We undertaken colony formation assay in vitro and tumor xenograft in vivo to detect the tumorigenicity of melanoma cells. In the present study, ZC3H15 was demonstrated highly expressed in melanoma tissues and cells. Elevated ZC3H15 impairs the survival of melanoma patients. Meanwhile, attenuation of ZC3H15 in melanoma cells inhibited cell proliferation and induced cycle arrest at G0/G1 phase. Consistently, the expression of cell cycle-related proteins cyclin dependent kinase 4 (CDK4), CDK6, and cyclin D1 (CCND1) was decreased while p21 was upregulated. Furthermore, we found the migration and invasion abilities were inhibited in ZC3H15-knockdown melanoma cells. In addition, downregulation of ZC3H15 resulted in inhibition of colony formation abilities in vitro and tumorigenesis in vivo. ZC3H15 promotes proliferation, migration/invasion, and tumorigenicity of melanoma cells. As a promising biomarker and therapeutic target in MM, ZC3H15 is worthy of further exploration.

Funder

Fundamental Research Funds for the Central Universities

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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