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ADCK2 Knockdown Affects the Migration of Melanoma Cells via MYL6.
Vierthaler, Marlene; Sun, Qian; Wang, Yiman; Steinfass, Tamara; Poelchen, Juliane; Hielscher, Thomas; Novak, Daniel; Umansky, Viktor; Utikal, Jochen.
Affiliation
  • Vierthaler M; Skin Cancer Unit, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
  • Sun Q; Department of Dermatology, Venereology and Allergology, University Medical Center Mannheim, Ruprecht Karl University of Heidelberg, 68167 Mannheim, Germany.
  • Wang Y; DKFZ-Hector Cancer Institute, University Medical Centre Mannheim, 68167 Mannheim, Germany.
  • Steinfass T; Faculty of Biosciences, Ruprecht Karl University, 69120 Heidelberg, Germany.
  • Poelchen J; Skin Cancer Unit, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
  • Hielscher T; Department of Dermatology, Venereology and Allergology, University Medical Center Mannheim, Ruprecht Karl University of Heidelberg, 68167 Mannheim, Germany.
  • Novak D; DKFZ-Hector Cancer Institute, University Medical Centre Mannheim, 68167 Mannheim, Germany.
  • Umansky V; Faculty of Biosciences, Ruprecht Karl University, 69120 Heidelberg, Germany.
  • Utikal J; Skin Cancer Unit, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Cancers (Basel) ; 14(4)2022 Feb 20.
Article in En | MEDLINE | ID: mdl-35205819
ABSTRACT

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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cancers (Basel) Year: 2022 Document type: Article Affiliation country: Alemania

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cancers (Basel) Year: 2022 Document type: Article Affiliation country: Alemania