Tumor Heterogeneity, Single-Cell Sequencing, and Drug Resistance
Tumor heterogeneity has been compared with Darwinian evolution and survival of the fittest. The evolutionary ecosystem of tumors consisting of heterogeneous tumor cell populations represents a considerable challenge to tumor therapy, since all genetically and phenotypically different subpopulations...
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doaj-e7d7a3f8958446a2a82c99ca2e7b9fa82020-11-25T01:59:20ZengMDPI AGPharmaceuticals1424-82472016-06-01923310.3390/ph9020033ph9020033Tumor Heterogeneity, Single-Cell Sequencing, and Drug ResistanceFelix Schmidt0Thomas Efferth1Department of Pharmaceutical Biology, Institute of Pharmacy and Biochemistry, Johannes Gutenberg University, Staudinger Weg 5, 55128 Mainz, GermanyDepartment of Pharmaceutical Biology, Institute of Pharmacy and Biochemistry, Johannes Gutenberg University, Staudinger Weg 5, 55128 Mainz, GermanyTumor heterogeneity has been compared with Darwinian evolution and survival of the fittest. The evolutionary ecosystem of tumors consisting of heterogeneous tumor cell populations represents a considerable challenge to tumor therapy, since all genetically and phenotypically different subpopulations have to be efficiently killed by therapy. Otherwise, even small surviving subpopulations may cause repopulation and refractory tumors. Single-cell sequencing allows for a better understanding of the genomic principles of tumor heterogeneity and represents the basis for more successful tumor treatments. The isolation and sequencing of single tumor cells still represents a considerable technical challenge and consists of three major steps: (1) single cell isolation (e.g., by laser-capture microdissection), fluorescence-activated cell sorting, micromanipulation, whole genome amplification (e.g., with the help of Phi29 DNA polymerase), and transcriptome-wide next generation sequencing technologies (e.g., 454 pyrosequencing, Illumina sequencing, and other systems). Data demonstrating the feasibility of single-cell sequencing for monitoring the emergence of drug-resistant cell clones in patient samples are discussed herein. It is envisioned that single-cell sequencing will be a valuable asset to assist the design of regimens for personalized tumor therapies based on tumor subpopulation-specific genetic alterations in individual patients.http://www.mdpi.com/1424-8247/9/2/33intratumoral heterogeneitytumor ecosystemssingle-cell sequencingmicromanipulationlaser-capture microdissectionflow cytometrynext generation sequencingRNA sequencingwhole genome amplificationmulti-region sequencingcirculating tumor cellsxenograft tumor modelscancer treatmentindividualized therapyprecision medicine |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Felix Schmidt Thomas Efferth |
spellingShingle |
Felix Schmidt Thomas Efferth Tumor Heterogeneity, Single-Cell Sequencing, and Drug Resistance Pharmaceuticals intratumoral heterogeneity tumor ecosystems single-cell sequencing micromanipulation laser-capture microdissection flow cytometry next generation sequencing RNA sequencing whole genome amplification multi-region sequencing circulating tumor cells xenograft tumor models cancer treatment individualized therapy precision medicine |
author_facet |
Felix Schmidt Thomas Efferth |
author_sort |
Felix Schmidt |
title |
Tumor Heterogeneity, Single-Cell Sequencing, and Drug Resistance |
title_short |
Tumor Heterogeneity, Single-Cell Sequencing, and Drug Resistance |
title_full |
Tumor Heterogeneity, Single-Cell Sequencing, and Drug Resistance |
title_fullStr |
Tumor Heterogeneity, Single-Cell Sequencing, and Drug Resistance |
title_full_unstemmed |
Tumor Heterogeneity, Single-Cell Sequencing, and Drug Resistance |
title_sort |
tumor heterogeneity, single-cell sequencing, and drug resistance |
publisher |
MDPI AG |
series |
Pharmaceuticals |
issn |
1424-8247 |
publishDate |
2016-06-01 |
description |
Tumor heterogeneity has been compared with Darwinian evolution and survival of the fittest. The evolutionary ecosystem of tumors consisting of heterogeneous tumor cell populations represents a considerable challenge to tumor therapy, since all genetically and phenotypically different subpopulations have to be efficiently killed by therapy. Otherwise, even small surviving subpopulations may cause repopulation and refractory tumors. Single-cell sequencing allows for a better understanding of the genomic principles of tumor heterogeneity and represents the basis for more successful tumor treatments. The isolation and sequencing of single tumor cells still represents a considerable technical challenge and consists of three major steps: (1) single cell isolation (e.g., by laser-capture microdissection), fluorescence-activated cell sorting, micromanipulation, whole genome amplification (e.g., with the help of Phi29 DNA polymerase), and transcriptome-wide next generation sequencing technologies (e.g., 454 pyrosequencing, Illumina sequencing, and other systems). Data demonstrating the feasibility of single-cell sequencing for monitoring the emergence of drug-resistant cell clones in patient samples are discussed herein. It is envisioned that single-cell sequencing will be a valuable asset to assist the design of regimens for personalized tumor therapies based on tumor subpopulation-specific genetic alterations in individual patients. |
topic |
intratumoral heterogeneity tumor ecosystems single-cell sequencing micromanipulation laser-capture microdissection flow cytometry next generation sequencing RNA sequencing whole genome amplification multi-region sequencing circulating tumor cells xenograft tumor models cancer treatment individualized therapy precision medicine |
url |
http://www.mdpi.com/1424-8247/9/2/33 |
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AT felixschmidt tumorheterogeneitysinglecellsequencinganddrugresistance AT thomasefferth tumorheterogeneitysinglecellsequencinganddrugresistance |
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