Innate lymphoid cells: potential targets for cancer therapeutics
被引:2
|
作者:
Ng, Chun Ki
论文数: 0引用数: 0
h-index: 0
机构:
Univ Queensland, Univ Queensland Diamantina Inst, Fac Med, Woolloongabba, Qld 4102, AustraliaUniv Queensland, Univ Queensland Diamantina Inst, Fac Med, Woolloongabba, Qld 4102, Australia
Ng, Chun Ki
[1
]
Belz, Gabrielle T.
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机构:
Univ Queensland, Univ Queensland Diamantina Inst, Fac Med, Woolloongabba, Qld 4102, AustraliaUniv Queensland, Univ Queensland Diamantina Inst, Fac Med, Woolloongabba, Qld 4102, Australia
Belz, Gabrielle T.
[1
]
机构:
[1] Univ Queensland, Univ Queensland Diamantina Inst, Fac Med, Woolloongabba, Qld 4102, Australia
来源:
TRENDS IN CANCER
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2023年
/
9卷
/
02期
基金:
英国医学研究理事会;
关键词:
TYRAMIDE SIGNAL AMPLIFICATION;
T-CELL;
NK CELLS;
RET PROTOONCOGENE;
STEM-CELLS;
IFN-GAMMA;
LUNG;
METASTASIS;
EXPRESSION;
PLASTICITY;
D O I:
10.1016/j.trecan.2022.10.007
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Innate lymphoid cells (ILCs) comprise a number of different subsets, including natural killer (NK) cells, ILC1s, ILC2s, ILC3s, and lymphoid tissue-inducer (LTi) cells that express receptors and signaling pathways that are highly responsive to continuously changing microenvironmental cues. In this Review, we highlight the key features of innate cells that define their capacity to respond rapidly to dif-ferent environments, how this ability can drive both tumor protection (limiting tumor development) or, alternatively, tumor progression, promoting tumor dis-semination and resistance to immunotherapy. We discuss how understanding the regulation of ILCs that can detect tumor cells early in a response opens the possibility of exploiting this functional plasticity to develop rational therapeutic strategies to bolster adaptive immune responses and improve patient outcomes.
机构:
Chinese Acad Sci, Inst Microbiol, CAS Key Lab Pathogen Microbiol & Immunol, Beijing 100101, Peoples R China
Univ Chinese Acad Sci, Beijing 100049, Peoples R ChinaChinese Acad Sci, Inst Microbiol, CAS Key Lab Pathogen Microbiol & Immunol, Beijing 100101, Peoples R China
Wang, Ziyu
Wang, Jun
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机构:
Chinese Acad Sci, Inst Microbiol, CAS Key Lab Pathogen Microbiol & Immunol, Beijing 100101, Peoples R China
Univ Chinese Acad Sci, Beijing 100049, Peoples R ChinaChinese Acad Sci, Inst Microbiol, CAS Key Lab Pathogen Microbiol & Immunol, Beijing 100101, Peoples R China
机构:
Chinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Gastroenterol, Beijing 100730, Peoples R ChinaChinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Gastroenterol, Beijing 100730, Peoples R China
Jiao, Yuhao
Yan, Zhiyu
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机构:
Chinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Gastroenterol, Beijing 100730, Peoples R China
Chinese Acad Med Sci & Peking Union Med Coll, MD Program 44, Beijing 100730, Peoples R ChinaChinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Gastroenterol, Beijing 100730, Peoples R China
Yan, Zhiyu
Yang, Aiming
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h-index: 0
机构:
Chinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Gastroenterol, Beijing 100730, Peoples R ChinaChinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Gastroenterol, Beijing 100730, Peoples R China
机构:
Univ Toronto, Temerty Fac Med, Dept Immunol, Toronto, ON, Canada
Univ Hlth Network, Toronto Gen Hosp Res Inst, Ajmera Transplant Ctr, Toronto, ON, CanadaUniv Toronto, Temerty Fac Med, Dept Immunol, Toronto, ON, Canada
Jegatheeswaran, Sinthuja
Mathews, Jessica A.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Hlth Network, Toronto Gen Hosp Res Inst, Ajmera Transplant Ctr, Toronto, ON, CanadaUniv Toronto, Temerty Fac Med, Dept Immunol, Toronto, ON, Canada
Mathews, Jessica A.
Crome, Sarah Q.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Toronto, Temerty Fac Med, Dept Immunol, Toronto, ON, Canada
Univ Hlth Network, Toronto Gen Hosp Res Inst, Ajmera Transplant Ctr, Toronto, ON, CanadaUniv Toronto, Temerty Fac Med, Dept Immunol, Toronto, ON, Canada