Inhibition of TASK-3 (KCNK9) channel biosynthesis changes cell morphology and decreases both DNA content and mitochondrial function of melanoma cells maintained in cell culture

Lívia Kosztka, Zoltán Rusznák, Dénes Nagy, Zsuzsanna Nagy, János Fodor, Géza Szucs, Andrea Telek, Mónika Gönczi, Olga Ruzsnavszky, Norbert Szentandrássy, László Csernoch

Research output: Article

23 Citations (Scopus)

Abstract

TASK-3 channel overexpression was shown to facilitate the survival of malignantly transformed cells, possibly by providing greater hypoxia tolerance through a still unknown mechanism. Although it has been suggested previously that TASK-3 channels are expressed in the mitochondrial membranes, their role here remains elusive. In this study, a transient transfection of TASK-3 knockdown melanoma cell cultures was produced to show the significance of TASK-3 expression. Reduction of the TASK-3 protein biosynthesis induced characteristic changes in cell morphology, reduced the amount of DNA and decreased metabolic activity and mitochondrial function of melanoma cells when compared with control. These findings indicate that TASK-3 channel expression and function is indispensable for the proliferation and/or survival of the melanoma cells, as they seem to contribute to their mitochondrial functions. The significance is that, in this study, we have shown that TASK-3 channels are expressed in the mitochondria of melanoma malignum cells, and they are essential for maintaining cellular integrity and viability. The TASK-3 knockdown melanoma cell line had altered morphology, reduced DNA content, decreased metabolic activity and impaired mitochondrial function. These data indicate that TASK-3 channels are functionally present in the mitochondria of the melanoma cells, and their function is essential for the survival of these cells, thus TASK-3 channels may be the possible targets of future anticancer therapy.

Original languageEnglish
Pages (from-to)308-322
Number of pages15
JournalMelanoma research
Volume21
Issue number4
DOIs
Publication statusPublished - aug. 1 2011

ASJC Scopus subject areas

  • Oncology
  • Dermatology
  • Cancer Research

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