Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Junaid, Muhammad, Lee, Aejin, Kim, Jaehyung, Park, Tae Jun, Lim, Su Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Molecular and Cellular Biology 2022
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
_version_ 1784784111372599296
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
work_keys_str_mv AT junaidmuhammad transcriptionalheterogeneityofcellularsenescenceincancer
AT leeaejin transcriptionalheterogeneityofcellularsenescenceincancer
AT kimjaehyung transcriptionalheterogeneityofcellularsenescenceincancer
AT parktaejun transcriptionalheterogeneityofcellularsenescenceincancer
AT limsubin transcriptionalheterogeneityofcellularsenescenceincancer