Tumour-associated macrophages and cancer

被引:201
作者
Cook, Jenny [1 ]
Hagemann, Thorsten [1 ]
机构
[1] John Vane Sci Ctr, Barts Canc Inst, Ctr Canc & Inflammat, London EC1M 6BQ, England
关键词
COLONY-STIMULATING FACTOR; INFLAMMATORY MONOCYTES; FACTOR-I; GM-CSF; EXPRESSION; POLARIZATION; DIFFERENTIATION; ANGIOGENESIS; PROGRESSION; STROMA;
D O I
10.1016/j.coph.2013.05.017
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Our understanding of the complex roles and functions of tumour-associated myeloid cells has improved vastly over the last few years. Alternatively activated macrophages, TAMs, are an abundant part of solid and haematological malignancies and have been linked with progression, metastasis and resistance to therapy. Still, characterisation and TAM targeting is hindered by a lack of TAM specific markers, but advances in next generation technologies are rapidly increasing our understanding of the sheer diversity of myeloid differentiation and phenotypic regulation. These technologies help to shed light on the heterogeneous phenotypic states of myeloid cells within the tumour. Alternative approaches to influence the myeloid compartment within cancers surround inhibition of myeloid recruitment or 're-education' of the plastic TAM phenotype. Our knowledge continuously grows on how even 'established' therapies might influence the myeloid compartment within tumours. Now the promising results from elegant pre-clinical studies at first translate into the clinic and use combination therapies with myeloid inhibitors and standard chemotherapy.
引用
收藏
页码:595 / 601
页数:7
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