Search Results - "Boshuizen, Julia"
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Cancer drug addiction is relayed by an ERK2-dependent phenotype switch
Published in Nature (London) (12-10-2017)“…The identification of an ERK2–JUNB–FRA1 signalling pathway that drives addiction to therapeutic drugs in cancer cells, and an ERK2-dependent phenotype switch…”
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Reversal of pre-existing NGFR-driven tumor and immune therapy resistance
Published in Nature communications (07-08-2020)“…Melanomas can switch to a dedifferentiated cell state upon exposure to cytotoxic T cells. However, it is unclear whether such tumor cells pre-exist in patients…”
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Ubiquitin ligase STUB1 destabilizes IFNγ-receptor complex to suppress tumor IFNγ signaling
Published in Nature communications (08-04-2022)“…The cytokine IFNγ differentially impacts on tumors upon immune checkpoint blockade (ICB). Despite our understanding of downstream signaling events, less is…”
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Author Correction: Reversal of pre-existing NGFR-driven tumor and immune therapy resistance
Published in Nature communications (07-02-2023)Get full text
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Mutationally-activated PI3’-kinase-α promotes de-differentiation of lung tumors initiated by the BRAFV600E oncoprotein kinase
Published in eLife (27-08-2019)“…Human lung adenocarcinoma exhibits a propensity for de-differentiation, complicating diagnosis and treatment, and predicting poorer patient survival. In…”
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TMED inhibition suppresses cell surface PD-1 expression and overcomes T cell dysfunction
Published in Journal for immunotherapy of cancer (07-11-2024)“…Background Blockade of the programmed cell death protein 1 (PD-1) immune checkpoint (ICB) is revolutionizing cancer therapy, but little is known about the…”
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Rational Cancer Treatment Combinations: An Urgent Clinical Need
Published in Molecular cell (18-06-2020)“…We are witnessing several revolutionary technological advances in cancer. These innovations have not only contributed to a growing understanding of the tumor…”
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Augmenting Immunotherapy Impact by Lowering Tumor TNF Cytotoxicity Threshold
Published in Cell (25-07-2019)“…New opportunities are needed to increase immune checkpoint blockade (ICB) benefit. Whereas the interferon (IFN)γ pathway harbors both ICB resistance factors…”
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Cooperative targeting of melanoma heterogeneity with an AXL antibody-drug conjugate and BRAF/MEK inhibitors
Published in Nature medicine (01-02-2018)“…Expression of AXL earmarks melanoma cells resistant to BRAF and MEK inhibitors that either pre-exist in treatment-naive tumors or emerge in response to…”
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Cooperative Targeting of Immunotherapy-Resistant Melanoma and Lung Cancer by an AXL-Targeting Antibody-Drug Conjugate and Immune Checkpoint Blockade
Published in Cancer research (Chicago, Ill.) (01-04-2021)“…Although immune checkpoint blockade (ICB) has shown remarkable clinical benefit in a subset of patients with melanoma and lung cancer, most patients experience…”
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Abstract 4591: Specific elimination of invasive and multidrug-resistant cancer cells by an antibody-drug conjugate targeting AXL
Published in Cancer research (Chicago, Ill.) (01-07-2017)“…Abstract Upon therapeutic pressure, cancers commonly select for drug-resistant, invasive subpopulations with elevated expression of the receptor tyrosine…”
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Multimodal stimulation screens reveal unique and shared genes limiting T cell fitness
Published in Cancer cell (08-04-2024)“…Genes limiting T cell antitumor activity may serve as therapeutic targets. It has not been systematically studied whether there are regulators that uniquely or…”
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Augmenting Immunotherapy Impact by Lowering Tumor TNF Cytotoxicity Threshold
Published in Cell (23-01-2020)Get full text
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Predictive Immune-Checkpoint Blockade Classifiers Identify Tumors Responding to Inhibition of PD-1 and/or CTLA-4
Published in Clinical cancer research (01-10-2021)“…Combining anti-PD-1 + anti-CTLA-4 immune-checkpoint blockade (ICB) shows improved patient benefit, but it is associated with severe immune-related adverse…”
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Mutationally-activated PI3'-kinase-α promotes de-differentiation of lung tumors initiated by the BRAF V600E oncoprotein kinase
Published in eLife (27-08-2019)“…Human lung adenocarcinoma exhibits a propensity for de-differentiation, complicating diagnosis and treatment, and predicting poorer patient survival. In…”
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BMN 673, a Novel and Highly Potent PARP1/2 Inhibitor for the Treatment of Human Cancers with DNA Repair Deficiency
Published in Clinical cancer research (15-09-2013)“…PARP1/2 inhibitors are a class of anticancer agents that target tumor-specific defects in DNA repair. Here, we describe BMN 673, a novel, highly potent PARP1/2…”
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