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Neutrophil diversity and plasticity in tumour progression and therapy

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NATURE REVIEWS CANCER
卷 20, 期 9, 页码 485-503

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NATURE PORTFOLIO
DOI: 10.1038/s41568-020-0281-y

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  1. Ministero dell'Istruzione, dell'Universita e della Ricerca (MIUR) [PRIN 2015YYKPNN, PRIN 2017K7FSYB, PRIN 20177J4E75]
  2. Ministero della Salute [GR-2016-02361263, GR-2016-02363531]
  3. Fondazione AIRC per la ricerca sul cancro [AIRC IG-19014, AIRC IG-22815, AIRC IG-20269]
  4. Fondazione AIRC per la ricerca sul cancro (AIRC Start-Up grant) [19141]
  5. Fondazione Umberto Veronesi (FUV)

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Neutrophils play a key role in defence against infection and in the activation and regulation of innate and adaptive immunity. In cancer, tumour-associated neutrophils (TANs) have emerged as an important component of the tumour microenvironment. Here, they can exert dual functions. TANs can be part of tumour-promoting inflammation by driving angiogenesis, extracellular matrix remodelling, metastasis and immunosuppression. Conversely, neutrophils can also mediate antitumour responses by direct killing of tumour cells and by participating in cellular networks that mediate antitumour resistance. Neutrophil diversity and plasticity underlie the dual potential of TANs in the tumour microenvironment. Myeloid checkpoints as well as the tumour and tissue contexture shape neutrophil function in response to conventional therapies and immunotherapy. We surmise that neutrophils can provide tools to tailor current immunotherapy strategies and pave the way to myeloid cell-centred therapeutic strategies, which would be complementary to current approaches. This Review discusses the emerging dual role played by neutrophils in the tumour microenvironment as part of tumour-promoting inflammation, while also mediating antitumour immune responses, and suggests that neutrophil function could be manipulated in myeloid cell-based therapeutic approaches to improve patient outcomes.

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