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Translational biology of osteosarcoma
被引:1012
|作者:
Kansara, Maya
[1
,2
]
Teng, Michele W.
[3
,4
,5
]
Smyth, Mark J.
[3
,4
,5
]
Thomas, David M.
[1
,2
,6
]
机构:
[1] Peter MacCallum Canc Ctr, Div Res, Melbourne, Vic 3002, Australia
[2] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Melbourne, Vic 3010, Australia
[3] OIMR Berghofer Med Res Inst, Immunol Canc & Infect Lab, Brisbane, Qld 4006, Australia
[4] OIMR Berghofer Med Res Inst, Canc Immunoregulat & Immunotherapy Lab, Brisbane, Qld 4006, Australia
[5] Univ Queensland, Sch Med, Herston, Qld 4006, Australia
[6] St Vincents Hosp, Garvan Inst Med Res, Kinghorn Canc Ctr, Darlinghurst, NSW 2010, Australia
基金:
澳大利亚国家健康与医学研究理事会;
英国医学研究理事会;
关键词:
HIGH-GRADE OSTEOSARCOMA;
CHILDRENS ONCOLOGY GROUP;
RAPAMYCIN INHIBITOR RIDAFOROLIMUS;
COMPARATIVE GENOMIC HYBRIDIZATION;
PRECLINICAL TESTING PROGRAM;
ROTHMUND-THOMSON-SYNDROME;
COLONY-STIMULATING FACTOR;
TUMOR-REJECTION ANTIGEN;
MESENCHYMAL STEM-CELLS;
GROWTH-FACTOR-I;
D O I:
10.1038/nrc3838
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
For the past 30 years, improvements in the survival of patients with osteosarcoma have been mostly incremental. Despite evidence of genomic instability and a high frequency of chromothripsis and kataegis, osteosarcomas carry few recurrent targetable mutations, and trials of targeted agents have been generally disappointing. Bone has a highly specialized immune environment and many immune signalling pathways are important in bone homeostasis. The success of the innate immune stimulant mifamurtide in the adjuvant treatment of non-metastatic osteosarconna suggests that newer immune-based treatments, such as immune checkpoint inhibitors, may substantially improve disease outcome.
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页码:722 / 735
页数:14
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