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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Main Authors: Marlene Vierthaler, Qian Sun, Yiman Wang, Tamara Steinfass, Juliane Poelchen, Thomas Hielscher, Daniel Novak, Viktor Umansky, Jochen Utikal
Format: Article
Language:English
Published: MDPI AG 2022-02-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/14/4/1071
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author Marlene Vierthaler
Qian Sun
Yiman Wang
Tamara Steinfass
Juliane Poelchen
Thomas Hielscher
Daniel Novak
Viktor Umansky
Jochen Utikal
author_facet Marlene Vierthaler
Qian Sun
Yiman Wang
Tamara Steinfass
Juliane Poelchen
Thomas Hielscher
Daniel Novak
Viktor Umansky
Jochen Utikal
author_sort Marlene Vierthaler
collection DOAJ
description 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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spelling doaj.art-7299160abc454fd4a611e43652e626082023-11-23T19:10:57ZengMDPI AGCancers2072-66942022-02-01144107110.3390/cancers14041071ADCK2 Knockdown Affects the Migration of Melanoma Cells via MYL6Marlene Vierthaler0Qian Sun1Yiman Wang2Tamara Steinfass3Juliane Poelchen4Thomas Hielscher5Daniel Novak6Viktor Umansky7Jochen Utikal8Skin Cancer Unit, German Cancer Research Center (DKFZ), 69120 Heidelberg, GermanySkin Cancer Unit, German Cancer Research Center (DKFZ), 69120 Heidelberg, GermanySkin Cancer Unit, German Cancer Research Center (DKFZ), 69120 Heidelberg, GermanySkin Cancer Unit, German Cancer Research Center (DKFZ), 69120 Heidelberg, GermanySkin Cancer Unit, German Cancer Research Center (DKFZ), 69120 Heidelberg, GermanyBiostatistik, German Cancer Research Center (DKFZ), 69120 Heidelberg, GermanySkin Cancer Unit, German Cancer Research Center (DKFZ), 69120 Heidelberg, GermanySkin Cancer Unit, German Cancer Research Center (DKFZ), 69120 Heidelberg, GermanySkin Cancer Unit, German Cancer Research Center (DKFZ), 69120 Heidelberg, GermanyBackground: 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.https://www.mdpi.com/2072-6694/14/4/1071melanomaADCK2MYL6motilitycancer
spellingShingle Marlene Vierthaler
Qian Sun
Yiman Wang
Tamara Steinfass
Juliane Poelchen
Thomas Hielscher
Daniel Novak
Viktor Umansky
Jochen Utikal
ADCK2 Knockdown Affects the Migration of Melanoma Cells via MYL6
Cancers
melanoma
ADCK2
MYL6
motility
cancer
title ADCK2 Knockdown Affects the Migration of Melanoma Cells via MYL6
title_full ADCK2 Knockdown Affects the Migration of Melanoma Cells via MYL6
title_fullStr ADCK2 Knockdown Affects the Migration of Melanoma Cells via MYL6
title_full_unstemmed ADCK2 Knockdown Affects the Migration of Melanoma Cells via MYL6
title_short ADCK2 Knockdown Affects the Migration of Melanoma Cells via MYL6
title_sort adck2 knockdown affects the migration of melanoma cells via myl6
topic melanoma
ADCK2
MYL6
motility
cancer
url https://www.mdpi.com/2072-6694/14/4/1071
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