ADCK2 knockdown affects the migration of melanoma cells via MYL6

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 ADCK...

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Hauptverfasser: Vierthaler, Marlene (VerfasserIn) , Sun, Qian (VerfasserIn) , Wang, Yiman (VerfasserIn) , Steinfass, Tamara (VerfasserIn) , Poelchen, Juliane (VerfasserIn) , Hielscher, Thomas (VerfasserIn) , Novak, Daniel (VerfasserIn) , Umansky, Viktor (VerfasserIn) , Utikal, Jochen (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 20 February 2022
In: Cancers
Year: 2022, Jahrgang: 14, Heft: 4, Pages: 1-18
ISSN:2072-6694
DOI:10.3390/cancers14041071
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.3390/cancers14041071
Verlag, kostenfrei, Volltext: https://www.mdpi.com/2072-6694/14/4/1071
Volltext
Verfasserangaben:Marlene Vierthaler, Qian Sun, Yiman Wang, Tamara Steinfass, Juliane Poelchen, Thomas Hielscher, Daniel Novak, Viktor Umansky, Jochen Utikal

MARC

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245 1 0 |a ADCK2 knockdown affects the migration of melanoma cells via MYL6  |c Marlene Vierthaler, Qian Sun, Yiman Wang, Tamara Steinfass, Juliane Poelchen, Thomas Hielscher, Daniel Novak, Viktor Umansky, Jochen Utikal 
246 3 3 |a ADCK two knockdown affects the migration of melanoma cells via MYL six 
246 3 3 |a ADCK 2 knockdown affects the migration of melanoma cells via MYL 6 
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520 |a 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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