In situ characterization of the tumor microenvironment

被引:1
|
作者
Sadeghirad, Habib [1 ]
Naei, Vahid Yaghoubi [1 ,2 ]
O'Byrne, Ken [3 ]
Warkiani, Majid E. [2 ]
Kulasinghe, Arutha [1 ]
机构
[1] Univ Queensland, Frazer Inst, Fac Med, Brisbane, Qld, Australia
[2] Univ Technol Sydney, Sch Biomed Engn, Sydney, NSW, Australia
[3] Princess Alexandra Hosp, Woolloongabba, Qld, Australia
关键词
HETEROGENEITY;
D O I
10.1016/j.copbio.2024.103083
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The development of new therapies for cancer is underpinned by an increasing need to comprehensively characterize the tumor microenvironment (TME). While traditional approaches have relied on bulk or single-cell approaches, these are limited in their ability to provide cellular context. Deconvolution of the complex TME is fundamental to understanding tumor dynamics and treatment resistance. Spatially resolved characterization of the TME is likely to provide greater insights into the cellular architecture, tumor-immune cell interactions, receptor-ligand interactions, and cell niches. In turn, these aid in dictating the optimal way in which to target each patient's individual cancer. In this review, we discuss a number of cutting-edge in situ spatial profiling methods giving us new insights into tumor biology.
引用
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页数:8
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