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Michael A. Beckett

Researcher at University of Chicago

Publications -  90
Citations -  13124

Michael A. Beckett is an academic researcher from University of Chicago. The author has contributed to research in topics: Radioresistance & Radiation therapy. The author has an hindex of 46, co-authored 88 publications receiving 11857 citations. Previous affiliations of Michael A. Beckett include Harvard University.

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Irradiation and anti–PD-L1 treatment synergistically promote antitumor immunity in mice

TL;DR: Evidence is provided for a close interaction between IR, T cells, and the PD-L1/PD-1 axis and a basis for the rational design of combination therapy with immune modulators and radiotherapy is established.
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STING-Dependent Cytosolic DNA Sensing Promotes Radiation-Induced Type I Interferon-Dependent Antitumor Immunity in Immunogenic Tumors

TL;DR: Radiation-mediated antitumor immunity in immunogenic tumors requires a functional cytosolic DNA-sensing pathway and suggests that cGAMP treatment might provide a new strategy to improve radiotherapy.
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Therapeutic effects of ablative radiation on local tumor require CD8+ T cells: changing strategies for cancer treatment

TL;DR: It is reported that reduction of tumor burden after ablative RT depends largely on T-cell responses, and the need for new strategies that not only reduce tumor burden but also enhance the role of antitumor immunity is emphasized.
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Blockade of the Vascular Endothelial Growth Factor Stress Response Increases the Antitumor Effects of Ionizing Radiation

TL;DR: It is reported that VEGF expression is induced in Lewis lung carcinomas (LLCs) both in vitro and in vivo after exposure to ionizing radiation (IR) and in human tumor cell lines (Seg-1 esophageal adenocarcinoma, SQ20B squamous cell carcinoma, T98 and U87 glioblastomas, and U1 melanoma) in vitro.
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Tumorigenic Keratinocyte Lines Requiring Anchorage and Fibroblast Support Cultured from Human Squamous Cell Carcinomas

TL;DR: It is demonstrated that SCC's often grow as established lines in culture, but they frequently possess in vitro growth requirements similar to those of normal keratinocytes.