Abstract

Kv1.5 (also known as KCNA5) is a protein encoded by the KCNA5 gene, which belongs to the voltage-gated potassium channel, shaker-related subfamily. Recently, a number of studies have suggested that Kv1.5 is overexpressed in numerous cancers and plays crucial roles in cancer development. However, until now, the expression and functions of Kv1.5 in osteosarcoma are still unclear. To characterize the potential biological functions of Kv1.5 in osteosarcoma, herein, we examined the expression levels of Kv1.5 in osteosarcoma cells and tissues using quantitative real-time polymerase chain reaction (qRT-PCR), western blot, and immunohistochemistry assays. Four short hairpin RNAs (shRNAs) targeting Kv1.5 were designed and homologous recombination technology was used to construct pGeneSil-Kv1.5 vectors. In addition, the vectors were transfected into osteosarcoma MG63 cells and Kv1.5 mRNA level was measured by qRT-PCR and the Kv1.5 protein level was examined by western blot. We also examined the effects of Kv1.5 silencing on proliferation, cell cycle and apoptosis of the osteosarcoma cells using CCK-8, colony formation, flow cytometry and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assays. Our results showed that Kv1.5 was aberrantly expressed in osteosarcoma and that the synthesized shRNA targeting Kv1.5 reduced Kv1.5 mRNA and protein expression effectively. Silencing Kv1.5 expression in the osteosarcoma cells significantly inhibited the proliferation of osteosarcoma cells, induced cell cycle arrest at G0/G1 phase, and induced cell apoptosis through up-regulation of p21, p27, Bax, Bcl-XL and caspase-3 and down-regulation of cyclins A, cyclins D1, cyclins E, Bcl-2 and Bik. In summary, our results indicate that Kv1.5 silencing could suppress osteosarcoma progression through multiple signaling pathways and suggest that Kv1.5 may be a novel target for osteosarcoma therapeutics.

Highlights

  • Osteosarcoma, originating in bone, is the most commonly encountered primary sarcoma, which accounts for 60% of total malignant childhood bone tumors [1]

  • The results of our study indicated that Kv1.5 mRNA and protein were aberrantly expressed in osteosarcoma and it regulated osteosarcoma cell proliferation, cell cycle and apoptosis

  • The results showed that positive Kv1.5 staining was detected in 15/23 (65.21%) osteosarcoma tissues and negative expression was found in six cases of osteosfibrous dysplasia

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Summary

Introduction

Osteosarcoma, originating in bone, is the most commonly encountered primary sarcoma, which accounts for 60% of total malignant childhood bone tumors [1]. A profound genetic instability was found to induce aberrant expression of several gene products, which is associated with osteosarcoma [5]. These genes might be potential targets for osteosarcoma treatment. Experimental research is urgently needed to characterize the biological functions of Kv1.5 in cancer, especially in osteosarcoma. To this end, we measured the expression levels of Kv1.5 in osteosarcoma using western blot, qRT-PCR and immunohistochemistry assays. The results of our study indicated that Kv1.5 mRNA and protein were aberrantly expressed in osteosarcoma and it regulated osteosarcoma cell proliferation, cell cycle and apoptosis. Our data suggest that Kv1.5 may regulate multiple signaling pathways to modulate cell cycle arrest and apoptosis

Results
Cell Culture
Western Blot Analysis
Sample Collection
Immunohistochemistry
Design and Synthesis of shRNA and PCR Primers
Construction of shRNA Plasmid and Cell Transfection
Cell Proliferation Assay
Colony Formation Assay
4.10. Flow Cytometry Analysis
4.11. Tunel Assay
4.12. Statistical Analysis
Full Text
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