MiR-375 Regulation of LDHB Plays Distinct Roles in Polyomavirus-Positive and -Negative Merkel Cell Carcinoma

被引:29
作者
Kumar, Satendra [1 ,2 ]
Xie, Hong [1 ,2 ,3 ,4 ]
Scicluna, Patrick [1 ,2 ,5 ]
Lee, Linkiat [1 ,2 ]
Bjornhagen, Viveca [6 ]
Hoog, Anders [1 ,2 ,7 ]
Larsson, Catharina [1 ,2 ,7 ]
Lui, Weng-Onn [1 ,2 ]
机构
[1] Karolinska Inst, Dept Oncol Pathol, SE-17176 Stockholm, Sweden
[2] Karolinska Univ Hosp, Canc Ctr Karolinska, SE-17176 Stockholm, Sweden
[3] Tianjin Med Univ, Sch Basic Med Sci, Tianjin Life Sci Res Ctr, Tianjin 300070, Peoples R China
[4] Tianjin Med Univ, Sch Basic Med Sci, Dept Pathogen Biol, Tianjin 300070, Peoples R China
[5] Karolinska Inst, Dept Cell & Mol Biol, SE-17165 Stockholm, Sweden
[6] Karolinska Univ Hosp, Dept Reconstruct Plast Surg, SE-17176 Stockholm, Sweden
[7] Karolinska Univ Hosp, Dept Clin Pathol & Cytol, SE-17176 Stockholm, Sweden
基金
中国国家自然科学基金;
关键词
Merkel cell carcinoma; Merkel cell polyomavirus; miR-375; LDHB; cell growth; SMALL T-ANTIGEN; LACTATE-DEHYDROGENASE-B; DOWN-REGULATION; MICRORNA-375; EXPRESSION; CANCER; PROLIFERATION; PROTEIN; HEAD; GENE;
D O I
10.3390/cancers10110443
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNA-375 (miR-375) is deregulated in multiple tumor types and regulates important targets involved in tumorigenesis and metastasis. This miRNA is highly expressed in Merkel cell carcinoma (MCC) compared to normal skin and other non-MCC skin cancers, and its expression is high in Merkel cell polyomavirus (MCPyV)-positive (MCPyV+) and low in MCPyV-negative (MCPyV-) MCC tumors. In this study, we characterized the function and target of miR-375 in MCPyV+ and MCPyV- MCC cell lines. Ectopic expression of miR-375 in MCPyV- MCC cells resulted in decreased cell proliferation and migration, as well as increased cell apoptosis and cell cycle arrest. However, in MCPyV+ MCC cells, inhibition of miR-375 expression reduced cell growth and induced apoptosis. Additionally, the expression of lactate dehydrogenase B (LDHB), a known target of miR-375, was inversely correlated with miR-375. Silencing of LDHB reduced cell growth in MCPyV- cell lines, while its silencing in MCPyV+ cell lines rescued the cell growth effect mediated by miR-375 inhibition. Together, our results suggest dual roles of miR-375 and LDHB in MCPyV and non-MCPyV-associated MCCs. We propose that LDHB could be a therapeutic target in MCC and different strategies should be applied in virus- and non-virus-associated MCCs.
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页数:16
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