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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Main Authors: Felix Schmidt, Thomas Efferth
Format: Article
Language:English
Published: MDPI AG 2016-06-01
Series:Pharmaceuticals
Subjects:
Online Access:http://www.mdpi.com/1424-8247/9/2/33
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spelling 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
work_keys_str_mv AT felixschmidt tumorheterogeneitysinglecellsequencinganddrugresistance
AT thomasefferth tumorheterogeneitysinglecellsequencinganddrugresistance
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