Wruck, Wasco, Bremmer, Felix, Kotthoff, Mara, Fichtner, Alexander, Skowron, Margaretha A. ORCID: 0000-0003-2152-384X, Schoenberger, Stefan, Calaminus, Gabriele, Vokuhl, Christian, Pfister, David, Heidenreich, Axel, Albers, Peter, Adjaye, James and Nettersheim, Daniel ORCID: 0000-0002-4483-845X (2021). The pioneer and differentiation factor FOXA2 is a key driver of yolk-sac tumour formation and a new biomarker for paediatric and adult yolk-sac tumours. J. Cell. Mol. Med., 25 (3). S. 1394 - 1406. HOBOKEN: WILEY. ISSN 1582-4934

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Abstract

Yolk-sac tumours (YSTs), a germ cell tumour subtype, occur in newborns and infants as well as in young adults of age 14-44 years. In clinics, adult patients with YSTs face a poor prognosis, as these tumours are often therapy-resistant and count for many germ cell tumour related deaths. So far, the molecular and (epi)genetic mechanisms that control development of YST are far from being understood. We deciphered the molecular and (epi)genetic mechanisms regulating YST formation by meta-analysing high-throughput data of gene and microRNA expression, DNA methylation and mutational burden. We validated our findings by qRT-PCR and immunohistochemical analyses of paediatric and adult YSTs. On a molecular level, paediatric and adult YSTs were nearly indistinguishable, but were considerably different from embryonal carcinomas, the stem cell precursor of YSTs. We identified FOXA2 as a putative key driver of YST formation, subsequently inducing AFP, GPC3, APOA1/APOB, ALB and GATA3/4/6 expression. In YSTs, WNT-, BMP- and MAPK signalling-related genes were up-regulated, while pluripotency- and (primordial) germ cell-associated genes were down-regulated. Expression of FOXA2 and related key factors seems to be regulated by DNA methylation, histone methylation / acetylation and microRNAs. Additionally, our results highlight FOXA2 as a promising new biomarker for paediatric and adult YSTs.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Wruck, WascoUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Bremmer, FelixUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kotthoff, MaraUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Fichtner, AlexanderUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Skowron, Margaretha A.UNSPECIFIEDorcid.org/0000-0003-2152-384XUNSPECIFIED
Schoenberger, StefanUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Calaminus, GabrieleUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Vokuhl, ChristianUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Pfister, DavidUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Heidenreich, AxelUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Albers, PeterUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Adjaye, JamesUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Nettersheim, DanielUNSPECIFIEDorcid.org/0000-0002-4483-845XUNSPECIFIED
URN: urn:nbn:de:hbz:38-592193
DOI: 10.1111/jcmm.16222
Journal or Publication Title: J. Cell. Mol. Med.
Volume: 25
Number: 3
Page Range: S. 1394 - 1406
Date: 2021
Publisher: WILEY
Place of Publication: HOBOKEN
ISSN: 1582-4934
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
Cell Biology; Medicine, Research & ExperimentalMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/59219

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