NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE101413 Query DataSets for GSE101413
Status Public on Apr 17, 2018
Title Tracking transcriptional changes in a species-specific manner during experimental hepatoblastoma progression in vivo
Organisms Gallus gallus; Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Hepatoblastoma is a primitive liver cancer occurring mainly in infants with defined molecular alterations driving its progression, which is difficult to model in vivo. Here we present a new animal model for hepatoblastoma on the chick chorioallantoic membrane (CAM), which recapitulates relevant features of hepatoblastoma in patients. Expression of classic tumor-associated proteins such as β-catenin, EpCAM and CK19 was maintained in acini-like organized tumors on CAM, as was synthesis of AFP, a tumor marker used for monitoring patient response. RNA sequencing revealed an unexpected molecular evolution of hepatoblastoma cells on the CAM, with significant deregulation of more than 6000 genes including more than half of all HOX genes. Bioinformatic analysis could clearly distinguish between tumor cell-expressed genes and chick host genes, thereby shedding new light on the complex interactions taking place during experimental hepatoblastoma progression. Importantly, human tumor suppressive ribosomal genes were downregulated after implantation, whereas mitochondrial genes encoding for anti-apoptotic peptides were strongly induced in vivo. Meprin-1α expression was increased during evolution of CAM tumors and confirmed by immunohistochemistry. Cisplatin, a commonly used chemotherapeutic agent for hepatoblastoma, showed significant anti-tumoral effects in this model. Our results broaden the understanding of the molecular adaptation process of human cancer cells to the microenvironment and might help to elaborate novel therapeutic concepts for the treatment of this pediatric liver tumor.
 
Overall design HuH6 cells and CAM mRNA profiles were generated by deep sequencing, in triplicate, using Illumina HiSeq 2500 and HiSeq 2000, respectively
 
Contributor(s) Hooks KB, Indersi E, Hagedorn M
Citation(s) 29662633
Submission date Jul 13, 2017
Last update date May 15, 2019
Contact name Katarzyna B Hooks
E-mail(s) katarzyna.hooks@gmail.com
Organization name Univ. Bordeaux
Department CBIB
Street address 146, rue Léo Saignat
City Bordeaux
ZIP/Postal code 33076
Country France
 
Platforms (3)
GPL11154 Illumina HiSeq 2000 (Homo sapiens)
GPL16133 Illumina HiSeq 2000 (Gallus gallus)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
Samples (22)
GSM2702310 E11 rep1
GSM2702311 E11 rep2
GSM2702312 E11 rep3
Relations
BioProject PRJNA394137
SRA SRP111862

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE101413_counts_mapped2GR38.txt.gz 781.8 Kb (ftp)(http) TXT
GSE101413_counts_mapped2galgal.txt.gz 455.5 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap