Search Results - "Koya, Richard C."
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Tunable-Combinatorial Mechanisms of Acquired Resistance Limit the Efficacy of BRAF/MEK Cotargeting but Result in Melanoma Drug Addiction
Published in Cancer cell (09-02-2015)“…Combined BRAF- and MEK-targeted therapy improves upon BRAF inhibitor (BRAFi) therapy but is still beset by acquired resistance. We show that melanomas acquire…”
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Inhibition of CSF-1 Receptor Improves the Antitumor Efficacy of Adoptive Cell Transfer Immunotherapy
Published in Cancer research (Chicago, Ill.) (2014)“…Colony stimulating factor 1 (CSF-1) recruits tumor-infiltrating myeloid cells (TIM) that suppress tumor immunity, including M2 macrophages and myeloid-derived…”
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3
Acquired resistance and clonal evolution in melanoma during BRAF inhibitor therapy
Published in Cancer discovery (01-01-2014)“…BRAF inhibitors elicit rapid antitumor responses in the majority of patients with BRAF(V600)-mutant melanoma, but acquired drug resistance is almost universal…”
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Host immunity contributes to the anti-melanoma activity of BRAF inhibitors
Published in The Journal of clinical investigation (01-03-2013)“…The BRAF mutant, BRAF(V600E), is expressed in nearly half of melanomas, and oral BRAF inhibitors induce substantial tumor regression in patients with…”
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BRAF Inhibitor Vemurafenib Improves the Antitumor Activity of Adoptive Cell Immunotherapy
Published in Cancer research (Chicago, Ill.) (15-08-2012)“…Combining immunotherapy with targeted therapy blocking oncogenic BRAFV600 may result in improved treatments for advanced melanoma. In this study, we developed…”
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CTLA4 Blockade Induces Frequent Tumor Infiltration by Activated Lymphocytes Regardless of Clinical Responses in Humans
Published in Clinical cancer research (15-06-2011)“…CTLA4 blocking monoclonal antibodies provide durable clinical benefit in a subset of patients with advanced melanoma mediated by intratumoral lymphocytic…”
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CTLA4 blockade increases Th17 cells in patients with metastatic melanoma
Published in Journal of translational medicine (20-05-2009)“…Th17 cells are CD4+ cells that produce interleukin 17 (IL-17) and are potent inducers of tissue inflammation and autoimmunity. We studied the levels of this T…”
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Human antigen-specific regulatory T cells generated by T cell receptor gene transfer
Published in PloS one (22-07-2010)“…Therapies directed at augmenting regulatory T cell (Treg) activities in vivo as a systemic treatment for autoimmune disorders and transplantation may be…”
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Antitumor activity from antigen-specific CD8 T cells generated in vivo from genetically engineered human hematopoietic stem cells
Published in Proceedings of the National Academy of Sciences - PNAS (20-12-2011)“…The goal of cancer immunotherapy is the generation of an effective, stable, and self-renewing antitumor T-cell population. One such approach involves the use…”
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Efficient identification of neoantigen-specific T-cell responses in advanced human ovarian cancer
Published in Journal for immunotherapy of cancer (20-06-2019)“…Efficient identification of neoantigen-specific T-cell responses in epithelial ovarian cancer (EOC) remains a challenge. Existing investigations of spontaneous…”
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11
WHSC1/NSD2 regulates immune infiltration in prostate cancer
Published in Journal for immunotherapy of cancer (01-02-2021)“…BackgroundImmunotherapy in prostate cancer (PCa) lags behind the progresses obtained in other cancer types partially because of its limited immune…”
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Kinetic phases of distribution and tumor targeting by T cell receptor engineered lymphocytes inducing robust antitumor responses
Published in Proceedings of the National Academy of Sciences - PNAS (10-08-2010)“…A key issue in advancing the use of adoptive cell transfer (ACT) of T cell receptor (TCR) engineered lymphocytes for cancer therapy is demonstrating how TCR…”
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13
A rare population of tumor antigen-specific CD4 + CD8 + double-positive αβ T lymphocytes uniquely provide CD8-independent TCR genes for engineering therapeutic T cells
Published in Journal for immunotherapy of cancer (09-01-2019)“…High-affinity tumor antigen-specific T-cell receptor (TCR) gene is required to engineer potent T cells for therapeutic treatment of cancer patients. However,…”
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Antitumor effects of the investigational selective MEK inhibitor TAK733 against cutaneous and uveal melanoma cell lines
Published in Molecular cancer (19-04-2012)“…TAK733 is a novel allosteric, non-ATP-binding, inhibitor of the BRAF substrates MEK-1/2. The growth inhibitory effects of TAK733 were assessed in a panel of 27…”
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Natural killer T cells in advanced melanoma patients treated with tremelimumab
Published in PloS one (22-10-2013)“…A significant barrier to effective immune clearance of cancer is loss of antitumor cytotoxic T cell activity. Antibodies to block pro-apoptotic/downmodulatory…”
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Host immunity contributes to the anti-melanoma activity of BRAF inhibitors
Published in The Journal of clinical investigation (01-01-2016)Get full text
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Decitabine immunosensitizes human gliomas to NY-ESO-1 specific T lymphocyte targeting through the Fas/Fas ligand pathway
Published in Journal of translational medicine (07-11-2011)“…The lack of effective treatments for gliomas makes them a significant health problem and highlights the need for the development of novel and innovative…”
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Modulation of cell signaling networks after CTLA4 blockade in patients with metastatic melanoma
Published in PloS one (15-09-2010)“…The effects on cell signalling networks upon blockade of cytotoxic T lymphocyte-associated antigen-4 (CTLA4) using the monoclonal antibody tremelimumab were…”
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Improved antitumor activity of immunotherapy with BRAF and MEK inhibitors in BRAF(V600E) melanoma
Published in Science translational medicine (18-03-2015)“…Combining immunotherapy and BRAF targeted therapy may result in improved antitumor activity with the high response rates of targeted therapy and the durability…”
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20
Single-cell analysis resolves the cell state transition and signaling dynamics associated with melanoma drug-induced resistance
Published in Proceedings of the National Academy of Sciences - PNAS (26-12-2017)“…Continuous BRAF inhibition of BRAF mutant melanomas triggers a series of cell state changes that lead to therapy resistance and escape from immune control…”
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