Search Tips

Transcriptome change mediated by tumor-intrinsic PRC2 inactivation in transplant murine breast cancer AT3 tumor model in C57BL/6J mice

UID: 11318

Author(s): Chi, Ping*, Chen, Yuedan*, Yan, Juan*, Chen, Yu* * MSK affiliated

Description
Description from GEO:

"We used CRISPR/Cas9-mediated knockout of PRC2 core components, Eed and generated PRC2-isogenic murine mammary tumor model (AT3, sgCon vs. sgEed ) amenable for syngeneic transplant in C57BL/6J mice. Transcriptome analysis of the explanted PRC2-wt (sgCon) and PRC2-loss (sgEed) AT3 tumors by RNA-seq demonstrated that PRC2 loss led to the upregulation of various developmental pathways, and the downregulation of both innate and adaptive immune response pathways."

Overall design from GEO:

"mRNA profiles of AT3 sgCon and sgEed tumors after mammary fat pad grafting in C57BL/6J mice"
Subject of Study
Subject(s)
Access via GEO


Accession #: GSE179703

Access via BioProject


Accession #: PRJNA744572

Access via SRA


Accession #: SRP327420

Access Restrictions
Free to All
Access Instructions
The NCBI Gene Expression Omnibus, BioProject, and SRA databases provide open access to these files.
Associated Publications
Equipment Used
Illumina HiSeq 2500
Dataset Format(s)
TXT
Dataset Size
587.3 KB
Data Catalog Record Updated
2024-08-14