Mutational Landscape of Virus- and UV-Associated Merkel Cell Carcinoma Cell Lines Is Comparable to Tumor Tissue
Merkel cell carcinoma (MCC) is a rare, highly aggressive cutaneous malignancy that is either associated with the integration of the Merkel cell polyomavirus or chronic UV exposure. These two types of carcinogenesis are reflected in characteristic mutational features present in MCC tumor lesions. How...
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doaj-85749e5ccb774371b5d640d763afb6312021-02-06T00:06:40ZengMDPI AGCancers2072-66942021-02-011364964910.3390/cancers13040649Mutational Landscape of Virus- and UV-Associated Merkel Cell Carcinoma Cell Lines Is Comparable to Tumor TissueKai Horny0Patricia Gerhardt1Angela Hebel-Cherouny2Corinna Wülbeck3Jochen Utikal4Jürgen C. Becker5Translational Skin Cancer Research, German Cancer Consortium (DKTK), 45141 Essen, GermanyDepartment of Dermatology, University Medicine Essen, 45141 Essen, GermanyDepartment of Dermatology, University Medicine Essen, 45141 Essen, GermanyDepartment of Dermatology, University Medicine Essen, 45141 Essen, GermanySkin Cancer Unit, German Cancer Research Center (DKFZ), 69120 Heidelberg, GermanyTranslational Skin Cancer Research, German Cancer Consortium (DKTK), 45141 Essen, GermanyMerkel cell carcinoma (MCC) is a rare, highly aggressive cutaneous malignancy that is either associated with the integration of the Merkel cell polyomavirus or chronic UV exposure. These two types of carcinogenesis are reflected in characteristic mutational features present in MCC tumor lesions. However, the genomic characteristics of MCC cell lines used as preclinical models are not well established. Thus, we analyzed the exomes of three virus-negative and six virus-positive MCC cell lines, all showing a classical neuroendocrine growth pattern. Virus-negative cell lines are characterized by a high tumor mutational burden (TMB), UV-light-induced DNA damage, functionally relevant coding mutations, e.g., in <i>RB1</i> and <i>TP53</i>, and large amounts of copy number variations (CNVs). In contrast, virus-positive cell lines have a low TMB with few coding mutations and lack prominent mutational signatures, but harbor characteristic CNVs. One of the virus-negative cell lines has a local <i>MYC</i> amplification associated with high <i>MYC</i> mRNA expression. In conclusion, virus-positive and -negative MCC cell lines with a neuroendocrine growth pattern resemble mutational features observed in MCC tissue samples, which strengthens their utility for functional studies.https://www.mdpi.com/2072-6694/13/4/649merkel cell carcinomamerkel cell polyoma virusUVcell lineMYCTP53 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kai Horny Patricia Gerhardt Angela Hebel-Cherouny Corinna Wülbeck Jochen Utikal Jürgen C. Becker |
spellingShingle |
Kai Horny Patricia Gerhardt Angela Hebel-Cherouny Corinna Wülbeck Jochen Utikal Jürgen C. Becker Mutational Landscape of Virus- and UV-Associated Merkel Cell Carcinoma Cell Lines Is Comparable to Tumor Tissue Cancers merkel cell carcinoma merkel cell polyoma virus UV cell line MYC TP53 |
author_facet |
Kai Horny Patricia Gerhardt Angela Hebel-Cherouny Corinna Wülbeck Jochen Utikal Jürgen C. Becker |
author_sort |
Kai Horny |
title |
Mutational Landscape of Virus- and UV-Associated Merkel Cell Carcinoma Cell Lines Is Comparable to Tumor Tissue |
title_short |
Mutational Landscape of Virus- and UV-Associated Merkel Cell Carcinoma Cell Lines Is Comparable to Tumor Tissue |
title_full |
Mutational Landscape of Virus- and UV-Associated Merkel Cell Carcinoma Cell Lines Is Comparable to Tumor Tissue |
title_fullStr |
Mutational Landscape of Virus- and UV-Associated Merkel Cell Carcinoma Cell Lines Is Comparable to Tumor Tissue |
title_full_unstemmed |
Mutational Landscape of Virus- and UV-Associated Merkel Cell Carcinoma Cell Lines Is Comparable to Tumor Tissue |
title_sort |
mutational landscape of virus- and uv-associated merkel cell carcinoma cell lines is comparable to tumor tissue |
publisher |
MDPI AG |
series |
Cancers |
issn |
2072-6694 |
publishDate |
2021-02-01 |
description |
Merkel cell carcinoma (MCC) is a rare, highly aggressive cutaneous malignancy that is either associated with the integration of the Merkel cell polyomavirus or chronic UV exposure. These two types of carcinogenesis are reflected in characteristic mutational features present in MCC tumor lesions. However, the genomic characteristics of MCC cell lines used as preclinical models are not well established. Thus, we analyzed the exomes of three virus-negative and six virus-positive MCC cell lines, all showing a classical neuroendocrine growth pattern. Virus-negative cell lines are characterized by a high tumor mutational burden (TMB), UV-light-induced DNA damage, functionally relevant coding mutations, e.g., in <i>RB1</i> and <i>TP53</i>, and large amounts of copy number variations (CNVs). In contrast, virus-positive cell lines have a low TMB with few coding mutations and lack prominent mutational signatures, but harbor characteristic CNVs. One of the virus-negative cell lines has a local <i>MYC</i> amplification associated with high <i>MYC</i> mRNA expression. In conclusion, virus-positive and -negative MCC cell lines with a neuroendocrine growth pattern resemble mutational features observed in MCC tissue samples, which strengthens their utility for functional studies. |
topic |
merkel cell carcinoma merkel cell polyoma virus UV cell line MYC TP53 |
url |
https://www.mdpi.com/2072-6694/13/4/649 |
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