TY - JOUR
T1 - Drug-tolerant persister cells in cancer
T2 - the cutting edges and future directions
AU - Pu, Yi
AU - Li, Lu
AU - Peng, Haoning
AU - Liu, Lunxu
AU - Heymann, Dominique
AU - Robert, Caroline
AU - Vallette, François
AU - Shen, Shensi
N1 - Publisher Copyright:
© 2023, Springer Nature Limited.
PY - 2023/11/1
Y1 - 2023/11/1
N2 - Drug-tolerant persister (DTP) cell populations were originally discovered in antibiotic-resistant bacterial biofilms. Similar populations with comparable features have since been identified among cancer cells and have been linked with treatment resistance that lacks an underlying genomic alteration. Research over the past decade has improved our understanding of the biological roles of DTP cells in cancer, although clinical knowledge of the role of these cells in treatment resistance remains limited. Nonetheless, targeting this population is anticipated to provide new treatment opportunities. In this Perspective, we aim to provide a clear definition of the DTP phenotype, discuss the underlying characteristics of these cells, their biomarkers and vulnerabilities, and encourage further research on DTP cells that might improve our understanding and enable the development of more effective anticancer therapies.
AB - Drug-tolerant persister (DTP) cell populations were originally discovered in antibiotic-resistant bacterial biofilms. Similar populations with comparable features have since been identified among cancer cells and have been linked with treatment resistance that lacks an underlying genomic alteration. Research over the past decade has improved our understanding of the biological roles of DTP cells in cancer, although clinical knowledge of the role of these cells in treatment resistance remains limited. Nonetheless, targeting this population is anticipated to provide new treatment opportunities. In this Perspective, we aim to provide a clear definition of the DTP phenotype, discuss the underlying characteristics of these cells, their biomarkers and vulnerabilities, and encourage further research on DTP cells that might improve our understanding and enable the development of more effective anticancer therapies.
UR - http://www.scopus.com/inward/record.url?scp=85172162909&partnerID=8YFLogxK
U2 - 10.1038/s41571-023-00815-5
DO - 10.1038/s41571-023-00815-5
M3 - Article
C2 - 37749382
AN - SCOPUS:85172162909
SN - 1759-4774
VL - 20
SP - 799
EP - 813
JO - Nature Reviews Clinical Oncology
JF - Nature Reviews Clinical Oncology
IS - 11
ER -