Identification of ERBB Pathway-Activated Cells in Triple-Negative Breast Cancer

Intratumor heterogeneity within a single tumor mass is one of the hallmarks of malignancy and has been reported in various tumor types. The molecular characterization of intratumor heterogeneity in breast cancer is a significant challenge for effective treatment. Using single-cell RNA sequencing (RN...

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Main Author: Soo Young Cho
Format: Article
Language:English
Published: BioMed Central 2019-03-01
Series:Genomics & Informatics
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Online Access:http://genominfo.org/upload/pdf/gi-2019-17-1-e3.pdf
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author Soo Young Cho
author_facet Soo Young Cho
author_sort Soo Young Cho
collection DOAJ
description Intratumor heterogeneity within a single tumor mass is one of the hallmarks of malignancy and has been reported in various tumor types. The molecular characterization of intratumor heterogeneity in breast cancer is a significant challenge for effective treatment. Using single-cell RNA sequencing (RNA-seq) data from a public resource, an ERBB pathway activated triple-negative cell population was identified. The differential expression of three subtyping marker genes (ERBB2, ESR1, and PGR) was not changed in the bulk RNA-seq data, but the single-cell transcriptomes showed intratumor heterogeneity. This result shows that ERBB signaling is activated using an indirect route and that the molecular subtype is changed on a single-cell level. Our data propose a different view on breast cancer subtypes, clarifying much confusion in this field and contributing to precision medicine.
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series Genomics & Informatics
spelling doaj-art-b68a0d0fd3894c39b135928aa1dd89b22025-02-02T13:28:54ZengBioMed CentralGenomics & Informatics2234-07422019-03-0117110.5808/GI.2019.17.1.e3546Identification of ERBB Pathway-Activated Cells in Triple-Negative Breast CancerSoo Young ChoIntratumor heterogeneity within a single tumor mass is one of the hallmarks of malignancy and has been reported in various tumor types. The molecular characterization of intratumor heterogeneity in breast cancer is a significant challenge for effective treatment. Using single-cell RNA sequencing (RNA-seq) data from a public resource, an ERBB pathway activated triple-negative cell population was identified. The differential expression of three subtyping marker genes (ERBB2, ESR1, and PGR) was not changed in the bulk RNA-seq data, but the single-cell transcriptomes showed intratumor heterogeneity. This result shows that ERBB signaling is activated using an indirect route and that the molecular subtype is changed on a single-cell level. Our data propose a different view on breast cancer subtypes, clarifying much confusion in this field and contributing to precision medicine.http://genominfo.org/upload/pdf/gi-2019-17-1-e3.pdfbreast neoplasmsERBB signaling pathwayintratumor heterogeneitymolecular subtypingsingle-cell RNA-seq
spellingShingle Soo Young Cho
Identification of ERBB Pathway-Activated Cells in Triple-Negative Breast Cancer
Genomics & Informatics
breast neoplasms
ERBB signaling pathway
intratumor heterogeneity
molecular subtyping
single-cell RNA-seq
title Identification of ERBB Pathway-Activated Cells in Triple-Negative Breast Cancer
title_full Identification of ERBB Pathway-Activated Cells in Triple-Negative Breast Cancer
title_fullStr Identification of ERBB Pathway-Activated Cells in Triple-Negative Breast Cancer
title_full_unstemmed Identification of ERBB Pathway-Activated Cells in Triple-Negative Breast Cancer
title_short Identification of ERBB Pathway-Activated Cells in Triple-Negative Breast Cancer
title_sort identification of erbb pathway activated cells in triple negative breast cancer
topic breast neoplasms
ERBB signaling pathway
intratumor heterogeneity
molecular subtyping
single-cell RNA-seq
url http://genominfo.org/upload/pdf/gi-2019-17-1-e3.pdf
work_keys_str_mv AT sooyoungcho identificationoferbbpathwayactivatedcellsintriplenegativebreastcancer