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Transcriptional Heterogeneity of Cellular Senescence in Cancer
Cellular senescence plays a paradoxical role in tumorigenesis through the expression of diverse senescence-associated (SA) secretory phenotypes (SASPs). The heterogeneity of SA gene expression in cancer cells not only promotes cancer stemness but also protects these cells from chemotherapy. Despite...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Molecular and Cellular Biology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9448649/ https://www.ncbi.nlm.nih.gov/pubmed/35983702 http://dx.doi.org/10.14348/molcells.2022.0036 |
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author | Junaid, Muhammad Lee, Aejin Kim, Jaehyung Park, Tae Jun Lim, Su Bin |
author_facet | Junaid, Muhammad Lee, Aejin Kim, Jaehyung Park, Tae Jun Lim, Su Bin |
author_sort | Junaid, Muhammad |
collection | PubMed |
description | Cellular senescence plays a paradoxical role in tumorigenesis through the expression of diverse senescence-associated (SA) secretory phenotypes (SASPs). The heterogeneity of SA gene expression in cancer cells not only promotes cancer stemness but also protects these cells from chemotherapy. Despite the potential correlation between cancer and SA biomarkers, many transcriptional changes across distinct cell populations remain largely unknown. During the past decade, single-cell RNA sequencing (scRNA-seq) technologies have emerged as powerful experimental and analytical tools to dissect such diverse senescence-derived transcriptional changes. Here, we review the recent sequencing efforts that successfully characterized scRNA-seq data obtained from diverse cancer cells and elucidated the role of senescent cells in tumor malignancy. We further highlight the functional implications of SA genes expressed specifically in cancer and stromal cell populations in the tumor microenvironment. Translational research leveraging scRNA-seq profiling of SA genes will facilitate the identification of novel expression patterns underlying cancer susceptibility, providing new therapeutic opportunities in the era of precision medicine. |
format | Online Article Text |
id | pubmed-9448649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Korean Society for Molecular and Cellular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-94486492022-09-13 Transcriptional Heterogeneity of Cellular Senescence in Cancer Junaid, Muhammad Lee, Aejin Kim, Jaehyung Park, Tae Jun Lim, Su Bin Mol Cells Minireview Cellular senescence plays a paradoxical role in tumorigenesis through the expression of diverse senescence-associated (SA) secretory phenotypes (SASPs). The heterogeneity of SA gene expression in cancer cells not only promotes cancer stemness but also protects these cells from chemotherapy. Despite the potential correlation between cancer and SA biomarkers, many transcriptional changes across distinct cell populations remain largely unknown. During the past decade, single-cell RNA sequencing (scRNA-seq) technologies have emerged as powerful experimental and analytical tools to dissect such diverse senescence-derived transcriptional changes. Here, we review the recent sequencing efforts that successfully characterized scRNA-seq data obtained from diverse cancer cells and elucidated the role of senescent cells in tumor malignancy. We further highlight the functional implications of SA genes expressed specifically in cancer and stromal cell populations in the tumor microenvironment. Translational research leveraging scRNA-seq profiling of SA genes will facilitate the identification of novel expression patterns underlying cancer susceptibility, providing new therapeutic opportunities in the era of precision medicine. Korean Society for Molecular and Cellular Biology 2022-09-30 2022-08-19 /pmc/articles/PMC9448649/ /pubmed/35983702 http://dx.doi.org/10.14348/molcells.2022.0036 Text en © The Korean Society for Molecular and Cellular Biology. All rights reserved. https://creativecommons.org/licenses/by-nc-sa/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ (https://creativecommons.org/licenses/by-nc-sa/3.0/) |
spellingShingle | Minireview Junaid, Muhammad Lee, Aejin Kim, Jaehyung Park, Tae Jun Lim, Su Bin Transcriptional Heterogeneity of Cellular Senescence in Cancer |
title | Transcriptional Heterogeneity of Cellular Senescence in Cancer |
title_full | Transcriptional Heterogeneity of Cellular Senescence in Cancer |
title_fullStr | Transcriptional Heterogeneity of Cellular Senescence in Cancer |
title_full_unstemmed | Transcriptional Heterogeneity of Cellular Senescence in Cancer |
title_short | Transcriptional Heterogeneity of Cellular Senescence in Cancer |
title_sort | transcriptional heterogeneity of cellular senescence in cancer |
topic | Minireview |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9448649/ https://www.ncbi.nlm.nih.gov/pubmed/35983702 http://dx.doi.org/10.14348/molcells.2022.0036 |
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