Single-cell RNA sequencing in melanoma: what have we learned so far?

被引:10
作者
Lim, Su Yin [1 ,2 ,3 ]
Rizos, Helen [1 ,2 ]
机构
[1] Macquarie Univ, Fac Med Hlth & Human Sci, Macquarie Med Sch, Sydney, Australia
[2] Melanoma Inst Australia, Sydney, Australia
[3] Macquarie Univ, Level 1,75 Talavera Rd, Sydney 2109, Australia
来源
EBIOMEDICINE | 2024年 / 100卷
基金
英国医学研究理事会;
关键词
Immunotherapies; MAPK inhibitors; Dedifferentiation; Cellular states; IMMUNE CHECKPOINT INHIBITORS; ACQUIRED-RESISTANCE; METASTATIC MELANOMA; PD-1; BLOCKADE; BRAF-MUTANT; HETEROGENEITY; MECHANISMS; DIFFERENTIATION; PROGRESSION; LANDSCAPE;
D O I
10.1016/j.ebiom.2024.104969
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Over the past decade, there have been remarkable improvements in the treatment and survival rates of melanoma patients. Treatment resistance remains a persistent challenge, however, and is partly attributable to intratumoural heterogeneity. Melanoma cells can transition through a series of phenotypic and transcriptional cell states that vary in invasiveness and treatment responsiveness. The diverse stromal and immune contexture of the tumour microenvironment also contributes to intratumoural heterogeneity and disparities in treatment response in melanoma patients. Recent advances in single -cell sequencing technologies have enabled a more detailed understanding of melanoma heterogeneity and the underlying transcriptional programs that regulate melanoma cell diversity and behaviour. In this review, we examine the concept of intratumoural heterogeneity and the challenges it poses to achieving long-lasting treatment responses. We focus on the significance of next generation single -cell sequencing in advancing our understanding of melanoma diversity and the unique insights gained from single -cell studies. Copyright (c) 2024 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
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页数:10
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