Cancers (Feb 2022)

ADCK2 Knockdown Affects the Migration of Melanoma Cells via MYL6

  • Marlene Vierthaler,
  • Qian Sun,
  • Yiman Wang,
  • Tamara Steinfass,
  • Juliane Poelchen,
  • Thomas Hielscher,
  • Daniel Novak,
  • Viktor Umansky,
  • Jochen Utikal

DOI
https://doi.org/10.3390/cancers14041071
Journal volume & issue
Vol. 14, no. 4
p. 1071

Abstract

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Background: ADCK2 is a member of the AarF domain-containing kinase family, which consists of five members, and has been shown to play a role in CoQ metabolism. However, ADCKs have also been connected to cancer cell survival, proliferation and motility. In this study, we investigated the role of ADCK2 in melanoma. Methods: The effect of ADCK2 on melanoma cell motility was evaluated by a scratch assay and a transwell invasion assay upon siRNA-mediated knockdown or stable overexpression of ADCK2. Results: We found that high levels of intratumoral ADCK2 and MYL6 are associated with a higher survival rate in melanoma patients. Knocking down ADCK2 resulted in enhanced cell migration of melanoma cells. Moreover, ADCK2-knockdown cells adopted a more dedifferentiated phenotype. A gene expression array revealed that the expression of ADCK2 correlated with the expressions of MYL6 and RAB2A. Knocking down MYL6 in ADCK2-overexpressing cells could abrogate the effect of ADCK2 overexpression and thus confirm the functional connection between ADCK2 and MYL6. Conclusion: ADCK2 affects melanoma cell motility, most probably via MYL6. Our results allow the conclusion that ADCK2 could act as a tumor suppressor in melanoma.

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