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Series GSE213396 Query DataSets for GSE213396
Status Public on Sep 19, 2023
Title Identification of a ΔNp63-dependent Basal-like A Subtype-specific Transcribed Enhancer Program (B-STEP) in Aggressive Pancreatic Ductal Adenocarcinoma [leChRO-seq]
Organism Homo sapiens
Experiment type Other
Summary A major hurdle to the application of precision oncology in pancreatic cancer is the lack of molecular stratification approaches and targeted therapy for defined molecular subtypes. In this work, we sought to gain further insight and identify molecular and epigenetic signatures of the basal-like A pancreatic ductal adenocarcinoma (PDAC) subgroup that can be applied to clinical samples for both patient stratification and for choice of therapy. We generated and integrated global gene expression and epigenome mapping data from patient-derived xenograft (PDX) models to identify subtype-specific enhancer regions that were validated in patient-derived samples. In addition, complementary nascent transcription and chromatin topology (HiChIP) analysis revealed a basal-like A subtype-specific transcribed enhancer program (B-STEP) in PDAC characterized by enhancer RNA (eRNA) production that is associated with higher chromatin interactions and subtype-specific gene activation. Importantly, we successfully confirmed the validity of eRNA detection as a possible histological approach for PDAC patient stratification by performing RNA in situ hybridization analyses for subtype-specific eRNAs on pathological tissue samples. Thus, the finding in this study provides proof-of-concept that subtype-specific epigenetic changes relevant for PDAC progression can be detected at a single cell level in complex, heterogeneous, primary tumor material.
 
Overall design Length extension chromatin run-on assay followed by sequencing (leChRO-Seq) was performed in L3.6pl cells in control or P63 knockdown condition as well as in pancreatic ductal adenocarcinoma (PDAC) patient derived xenograft (PDX) tissue with basal-like A phenotype.
 
Contributor(s) Najafova Z, Johnsen SA
Citation(s) 37279184
Submission date Sep 14, 2022
Last update date Sep 19, 2023
Contact name Steven A. Johnsen
Organization name Robert Bosch Center for Tumor Diseases
Lab Molecular Cancer Epigenetics
Street address Auerbachstraße 112
City Stuttgart
State/province BW
ZIP/Postal code 70376
Country Germany
 
Platforms (1)
GPL20301 Illumina HiSeq 4000 (Homo sapiens)
Samples (5)
GSM6585589 L36_leChRO_NT5_Rep1
GSM6585590 L36_leChRO_NT5_Rep2
GSM6585591 L36_leChRO_sip63_Rep1
This SubSeries is part of SuperSeries:
GSE213397 Identification of a ΔNp63-dependent Basal-like A Subtype-specific Transcribed Enhancer Program (B-STEP) in Aggressive Pancreatic Ductal Adenocarcinoma
Relations
BioProject PRJNA880825

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
GSE213396_GPDX4_leChRO_minus.bw 16.6 Mb (ftp)(http) BW
GSE213396_GPDX4_leChRO_plus.bw 17.2 Mb (ftp)(http) BW
GSE213396_L36_leChRO_NT5_minus.bw 92.7 Mb (ftp)(http) BW
GSE213396_L36_leChRO_NT5_plus.bw 96.1 Mb (ftp)(http) BW
GSE213396_L36_leChRO_siP63_minus.bw 84.6 Mb (ftp)(http) BW
GSE213396_L36_leChRO_siP63_plus.bw 87.6 Mb (ftp)(http) BW
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Raw data are available in SRA
Processed data are available on Series record

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