دورية أكاديمية

The Immune Microenvironment Confers Resistance to MAPK Pathway Inhibitors through Macrophage-Derived TNF alpha

التفاصيل البيبلوغرافية
العنوان: The Immune Microenvironment Confers Resistance to MAPK Pathway Inhibitors through Macrophage-Derived TNF alpha
المؤلفون: Smith, MP, Sanchez-Laorden, B, O Brien, K, Brunton, H, Ferguson, J, Young, H, Dhomen, N, Flaherty, KT, Frederick, DT, Cooper, ZA, Wargo, JA, Marais, R, Wellbrock, C
المساهمون: Marais, Richard Malcolm
بيانات النشر: AMER ASSOC CANCER RESEARCH
سنة النشر: 2018
المجموعة: The Institute of Cancer Research (ICR): Publications Repository
الوصف: Recently, the rationale for combining targeted therapy with immunotherapy has come to light, but our understanding of the immune response during MAPK pathway inhibitor treatment is limited. We discovered that the immune microenvironment can act as a source of resistance to MAPK pathway-targeted therapy, and moreover during treatment this source becomes reinforced. In particular, we identified macrophage-derived TNF alpha as a crucial melanoma growth factor that provides resistance to MAPK pathway inhibitors through the lineage transcription factor MITF (microphthalmia transcription factor). Most strikingly, in BRAF-mutant melanomas of patients and BRAF(V600E) melanoma allografts, MAPK pathway inhibitors increased the number of tumor-associated macrophages, and TNF alpha and MITF expression. Inhibiting TNF alpha signaling with I kappa B kinase inhibitors profoundly enhanced the efficacy of MAPK pathway inhibitors by targeting not only the melanoma cells but also the microenvironment. In summary, we identify the immune microenvironment as a novel source of resistance and reveal a new strategy to improve the efficacy of targeted therapy in melanoma. SIGNIFICANCE: This study identifies the immune microenvironment as a source of resistance to MAPK pathway inhibitors through macrophage-derived TNF alpha, and reveals that in patients on treatment this source becomes reinforced. Inhibiting I kappa B kinase enhances the efficacy of MAPK pathway inhibitors, which identifies this approach as a potential novel strategy to improve targeted therapy in melanoma. (C) 2014 AACR.
نوع الوثيقة: article in journal/newspaper
وصف الملف: 1229; application/pdf
اللغة: English
تدمد: 2159-8274
2159-8290
العلاقة: 10; CANCER DISCOVERY, 2014, 4 pp. 1214 - 1229; https://repository.icr.ac.uk/handle/internal/2255Test
DOI: 10.1158/2159-8290.CD-13-1007
الإتاحة: https://doi.org/10.1158/2159-8290.CD-13-1007Test
https://repository.icr.ac.uk/handle/internal/2255Test
حقوق: https://www.rioxx.net/licenses/all-rights-reservedTest
رقم الانضمام: edsbas.A8682222
قاعدة البيانات: BASE
الوصف
تدمد:21598274
21598290
DOI:10.1158/2159-8290.CD-13-1007