Gene Expression Nebulas
A data portal of transcriptomic profiles analyzed by a unified pipeline across multiple species

Gene Expression Nebulas

A data portal of transcriptome profiles across multiple species

PRJNA464359: Stromal Fibroblasts Drive Single Cell Heterogeneity in Pancreatic Cancer

Source: NCBI / GSE113616
Submission Date: Apr 24 2018
Release Date: Apr 24 2019
Update Date: Jun 06 2019

Summary: To understand the interplay between cancer and stroma, we performed single cell RNA-sequencing of PDAC cells admixed with stromal fibroblasts and defined different single cell populations with varying levels of proliferative and metastatic transcriptional states. PDAC cell behavior in vitro and in vivo on these phenotypic axes could be tuned with the proportion of stromal fibroblasts. These cell types were identified in human pancreatic tumors, and specific subpopulations were associated with worsened outcomes.

Overall Design: 92 single PDAC cells and 92 single CAF cells were micromanipulated and prepared for sequencing (23 of each cell type from four culture ratios). The 24th sample from each cell type-culture condition combination is a population control obtained by micromanipulating 100 cells of the given type from the given culture condition and preparing it as if it were a single cell, giving a total of 96 PDAC samples and 96 CAF samples. During the course of library construction, 3 samples were lost, all PDAC cells from the 30:70 condition (two single cells and the population control), leaving 93 total PDAC samples and 96 total CAF samples.

GEN Datasets:
GEND000051
Strategy:
Species:
Healthy Condition:
Cell Line:
Protocol
Growth Protocol: PDAC cells and CAFs were seeded in 6-well plates in 5 different ratios: 100% PDAC, 50:50 PDAC:CAF, 30:70 PDAC:CAF, 10:90 PDAC:CAF, and 100% CAF. DMEM (high glucose, pyruvate) with 10% fetal bovine serum (FBS) and 100 U/mL Penicillin and 100 mg/mL Streptomycin was used for all cultures.
Treatment Protocol: -
Extract Protocol: After 72 hours of culture, cells were trypsinized and resuspended in PBS solution, and micromanipulated. PDAC cells or CAFs were then individually micromanipulated using a 10 m transfer tip on an Eppendorf TransferMan NK2 micromanipulator, transferred into PCR tubes containing RNA protective lysis buffer (Clontech Laboratories), and flash frozen in liquid nitrogen.
Library Construction Protocol: -
Sequencing
Molecule Type: poly(A)+ RNA
Library Source:
Library Layout: PAIRED
Library Strand: -
Platform: ILLUMINA
Instrument Model: Illumina HiSeq 2000
Strand-Specific: Unspecific
Samples
Basic Information:
Sample Characteristic:
Biological Condition:
Experimental Variables:
Protocol:
Sequencing:
Assessing Quality:
Analysis:
Data Resource GEN Sample ID GEN Dataset ID Project ID BioProject ID Sample ID Sample Name BioSample ID Sample Accession Experiment Accession Release Date Submission Date Update Date Species Race Ethnicity Age Age Unit Gender Source Name Tissue Cell Type Cell Subtype Cell Line Disease Disease State Development Stage Mutation Phenotype Case Detail Control Detail Growth Protocol Treatment Protocol Extract Protocol Library Construction Protocol Molecule Type Library Layout Strand-Specific Library Strand Spike-In Strategy Platform Instrument Model Cell Number Reads Number Gbases AvgSpotLen1 AvgSpotLen2 Uniq Mapping Rate Multiple Mapping Rate Coverage Rate
Publications
Stromal Microenvironment Shapes the Intratumoral Architecture of Pancreatic Cancer.
Cell . 2019-05-30 [PMID: 31155233]