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  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Doi.org Make Money
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We began analyzing https://www.nature.com/articles/nrclinonc.2016.217, but it redirected us to https://www.nature.com/articles/nrclinonc.2016.217. The analysis below is for the second page.

Title[redir]:
Tumour-associated macrophages as treatment targets in oncology | Nature Reviews Clinical Oncology
Description:
Tumour-associated macrophages (TAMs) are key drivers of tumour-promoting inflammation and cancer progression, and are important determinants of responsiveness to a range of therapies. Herein, the authors summarize the roles of TAMs in cancer, and discuss the potential of TAM-targeted therapeutic strategies to complement and synergize with other anticancer treatments. Macrophages are crucial drivers of tumour-promoting inflammation. Tumour-associated macrophages (TAMs) contribute to tumour progression at different levels: by promoting genetic instability, nurturing cancer stem cells, supporting metastasis, and taming protective adaptive immunity. TAMs can exert a dual, yin–yang influence on the effectiveness of cytoreductive therapies (chemotherapy and radiotherapy), either antagonizing the antitumour activity of these treatments by orchestrating a tumour-promoting, tissue-repair response or, instead, enhancing the overall antineoplastic effect. TAMs express molecular triggers of checkpoint proteins that regulate T-cell activation, and are targets of certain checkpoint-blockade immunotherapies. Other macrophage-centred approaches to anticancer therapy are under investigation, and include: inhibition of macrophage recruitment to, and/or survival in, tumours; functional re-education of TAMs to an antitumour,

Matching Content Categories {📚}

  • Education
  • Health & Fitness
  • Science

Content Management System {📝}

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Custom-built

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Traffic Estimate {📈}

What is the average monthly size of doi.org audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


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Keywords {🔍}

pubmed, google, scholar, cas, cancer, central, macrophages, macrophage, cells, cell, tumor, res, tumorassociated, nature, immunol, mantovani, med, nat, patients, oncol, article, immunity, therapy, factor, clin, antitumor, blockade, targeting, science, immune, receptor, anticancer, human, antibody, metastasis, survival, rev, breast, natl, content, progression, chemotherapy, inhibition, exp, monocytes, pancreatic, lymphoma, clinical, microenvironment, tumour,

Topics {✒️}

nature portfolio journals permissions reprints nature portfolio privacy policy colony-stimulating factor-1 receptor ipilimumab-dependent cell-mediated cytotoxicity pi3k/akt/rhoa signaling pathway cox/mpges-1/pge2 pathway depicts advertising european research council worldwide cancer research macrophage colony-stimulating factor-1 macrophage colony-stimulating factor anti-csf-1r antibody reveals antibody-dependent cellular cytotoxicity social media cancer research tenosynovial giant-cell tumor anti-pd-l1 antibody mpdl3280a anti-cd47 antibody-mediated phagocytosis colony-stimulating factor-1 open-label cancer stem/initiating cells author information authors nature+ nature 454 nature 228 nature 475 nature 515 nature myeloid-derived suppressor cells t-cell checkpoint immunotherapy targeting cgas-sting pathway csf1 receptor targeting author correspondence intra-tumoral infiltrating macrophages facilitate breast-tumour metastasis her2-positive breast cancer provide tools tam-focused therapeutic strategies macrophage-activating signal factor hypoxia enhanced mdsc-mediated anti-cd47 antibody synergizes small-cell lung cancer csf1r kinase tumour-targeting monoclonal antibodies antitumor t-cell immunity vegf receptor flt-1 phase ii study microsatellite-unstable gastric carcinoma

Questions {❓}

  • Inflammation and cancer: back to Virchow?
  • Innate inflammation and cancer: is it time for cancer prevention?
  • Neutralizing tumor-promoting chronic inflammation: a magic bullet?

Schema {🗺️}

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         headline:Tumour-associated macrophages as treatment targets in oncology
         description: Tumour-associated macrophages (TAMs) are key drivers of tumour-promoting inflammation and cancer progression, and are important determinants of responsiveness to a range of therapies. Herein, the authors summarize the roles of TAMs in cancer, and discuss the potential of TAM-targeted therapeutic strategies to complement and synergize with other anticancer treatments. Macrophages are crucial drivers of tumour-promoting inflammation. Tumour-associated macrophages (TAMs) contribute to tumour progression at different levels: by promoting genetic instability, nurturing cancer stem cells, supporting metastasis, and taming protective adaptive immunity. TAMs can exert a dual, yin–yang influence on the effectiveness of cytoreductive therapies (chemotherapy and radiotherapy), either antagonizing the antitumour activity of these treatments by orchestrating a tumour-promoting, tissue-repair response or, instead, enhancing the overall antineoplastic effect. TAMs express molecular triggers of checkpoint proteins that regulate T-cell activation, and are targets of certain checkpoint-blockade immunotherapies. Other macrophage-centred approaches to anticancer therapy are under investigation, and include: inhibition of macrophage recruitment to, and/or survival in, tumours; functional re-education of TAMs to an antitumour, 'M1-like' mode; and tumour-targeting monoclonal antibodies that elicit macrophage-mediated extracellular killing, or phagocytosis and intracellular destruction of cancer cells. The evidence supporting these strategies is reviewed herein. We surmise that TAMs can provide tools to tailor the use of cytoreductive therapies and immunotherapy in a personalized medicine approach, and that TAM-focused therapeutic strategies have the potential to complement and synergize with both chemotherapy and immunotherapy.
         datePublished:2017-01-24T00:00:00Z
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External Links {🔗}(781)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Prism.js
  • Zoom.js

Emails and Hosting {✉️}

Mail Servers:

  • mx.zoho.eu
  • mx2.zoho.eu
  • mx3.zoho.eu

Name Servers:

  • josh.ns.cloudflare.com
  • zita.ns.cloudflare.com

CDN Services {📦}

  • Crossref

6.09s.