Abstract

Breast cancer is the most common malignant tumor in women, and its incidence is increasing each year. To effectively treat breast cancer, it is important to identify genes involved in its occurrence and development and to exploit them as potential drug therapy targets. Here, we found that potassium channel subfamily K member 6 (KCNK6) is significantly overexpressed in breast cancer, however, its function in tumors has not been reported. We further verified that KCNK6 expression is upregulated in breast cancer biopsies. Moreover, overexpressed KCNK6 was found to enhance the proliferation, invasion, and migration ability of breast cancer cells. These effects may occur by weakening cell adhesion and reducing cell hardness, thus affecting the malignant phenotype of breast cancer cells. Our study confirmed, for the first time, that increased KCNK6 expression in breast cancer cells may promote their proliferation, invasion, and migration. Moreover, considering that ion channels serve as therapeutic targets for many small molecular drugs in clinical treatment, targeting KCNK6 may represent a novel strategy for breast cancer therapies. Hence, the results of this study provide a theoretical basis for KCNK6 to become a potential molecular target for breast cancer treatment in the future.

Highlights

  • The latest global cancer data released by the international cancer research agency (IARC) of the World Health Organization, show that in 2020, the number of new breast cancer cases worldwide was as high as 2.26 million, with an approximated 680,000 associated female deaths, far exceeding that of any other female cancer

  • We found that the expression of potassium channel protein KCNK6 in normal breast tissue was significantly lower than that in breast cancer tissue (P < 0.05; Figures 1A– C)

  • Through the data mining of two groups of breast cancer gene expression profile microarray datasets, we found that the potassium channel protein KCNK6 was expressed at an abnormally high level in breast cancer cells

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Summary

Introduction

The latest global cancer data released by the international cancer research agency (IARC) of the World Health Organization, show that in 2020, the number of new breast cancer cases worldwide was as high as 2.26 million, with an approximated 680,000 associated female deaths, far exceeding that of any other female cancer. With the development of modern oncology, the unrestricted proliferation of tumor cells, leading to their invasion and metastasis, has been confirmed as the fundamental cause of breast cancer progression and patient death (Chaffer et al, 2016; Mittal, 2018). It is, of urgency to predict the biological behavior of breast cancer by studying the proliferation, invasion, and metastasis of cancer cells, while seeking to identify genes and potential targets involved in the occurrence and development of breast cancer

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