Single-cell sequencing in translational cancer research and challenges to meet clinical diagnostic needs
(2021) In Genes, Chromosomes and Cancer 60(7). p.504-524- Abstract
The ability to capture alterations in the genome or transcriptome by next-generation sequencing has provided critical insight into molecular changes and programs underlying cancer biology. With the rapid technological development in single-cell sequencing, it has become possible to study individual cells at the transcriptional, genetic, epigenetic, and protein level. Using single-cell analysis, an increased resolution of fundamental processes underlying cancer development is obtained, providing comprehensive insights otherwise lost by sequencing of entire (bulk) samples, in which molecular signatures of individual cells are averaged across the entire cell population. Here, we provide a concise overview on the application of single-cell... (More)
The ability to capture alterations in the genome or transcriptome by next-generation sequencing has provided critical insight into molecular changes and programs underlying cancer biology. With the rapid technological development in single-cell sequencing, it has become possible to study individual cells at the transcriptional, genetic, epigenetic, and protein level. Using single-cell analysis, an increased resolution of fundamental processes underlying cancer development is obtained, providing comprehensive insights otherwise lost by sequencing of entire (bulk) samples, in which molecular signatures of individual cells are averaged across the entire cell population. Here, we provide a concise overview on the application of single-cell analysis of different modalities within cancer research by highlighting key articles of their respective fields. We furthermore examine the potential of existing technologies to meet clinical diagnostic needs and discuss current challenges associated with this translation.
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- author
- Pfisterer, Ulrich LU ; Bräunig, Julia LU ; Brattås, Per LU ; Heidenblad, Markus LU ; Karlsson, Göran LU and Fioretos, Thoas LU
- organization
-
- Center for Translational Genomics (CTG)
- LUCC: Lund University Cancer Centre
- Translational Genomic and Functional Studies of Leukemia (research group)
- Division of Clinical Genetics
- Stem Cells and Leukemia (research group)
- Division of Molecular Hematology (DMH)
- StemTherapy: National Initiative on Stem Cells for Regenerative Therapy
- Department of Laboratory Medicine
- publishing date
- 2021-07-01
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Genes, Chromosomes and Cancer
- volume
- 60
- issue
- 7
- pages
- 21 pages
- publisher
- John Wiley & Sons Inc.
- external identifiers
-
- scopus:85102467396
- pmid:33611828
- ISSN
- 1045-2257
- DOI
- 10.1002/gcc.22944
- language
- English
- LU publication?
- yes
- id
- e7315982-eb86-4e80-9d3a-4dfb515e02ed
- date added to LUP
- 2021-03-26 12:12:44
- date last changed
- 2024-11-02 23:06:14
@article{e7315982-eb86-4e80-9d3a-4dfb515e02ed, abstract = {{<p>The ability to capture alterations in the genome or transcriptome by next-generation sequencing has provided critical insight into molecular changes and programs underlying cancer biology. With the rapid technological development in single-cell sequencing, it has become possible to study individual cells at the transcriptional, genetic, epigenetic, and protein level. Using single-cell analysis, an increased resolution of fundamental processes underlying cancer development is obtained, providing comprehensive insights otherwise lost by sequencing of entire (bulk) samples, in which molecular signatures of individual cells are averaged across the entire cell population. Here, we provide a concise overview on the application of single-cell analysis of different modalities within cancer research by highlighting key articles of their respective fields. We furthermore examine the potential of existing technologies to meet clinical diagnostic needs and discuss current challenges associated with this translation.</p>}}, author = {{Pfisterer, Ulrich and Bräunig, Julia and Brattås, Per and Heidenblad, Markus and Karlsson, Göran and Fioretos, Thoas}}, issn = {{1045-2257}}, language = {{eng}}, month = {{07}}, number = {{7}}, pages = {{504--524}}, publisher = {{John Wiley & Sons Inc.}}, series = {{Genes, Chromosomes and Cancer}}, title = {{Single-cell sequencing in translational cancer research and challenges to meet clinical diagnostic needs}}, url = {{http://dx.doi.org/10.1002/gcc.22944}}, doi = {{10.1002/gcc.22944}}, volume = {{60}}, year = {{2021}}, }