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DHODH-mediated ferroptosis defence is a targetable vulnerability in cancer

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  1. Article

    Open Access

    Author Correction: 3-Phosphoinositide-dependent kinase 1 drives acquired resistance to osimertinib

    Ismail M. Meraz, Mourad Majidi, Bingliang Fang, Feng Meng in Communications Biology (2023)

  2. Article

    Open Access

    3-Phosphoinositide-dependent kinase 1 drives acquired resistance to osimertinib

    Osimertinib sensitive and resistant NSCLC NCI-H1975 clones are used to model osimertinib acquired resistance in humanized and non-humanized mice and delineate potential resistance mechanisms. No new EGFR mutat...

    Ismail M. Meraz, Mourad Majidi, Bingliang Fang, Feng Meng in Communications Biology (2023)

  3. Article

    Open Access

    CombPDX: a unified statistical framework for evaluating drug synergism in patient-derived xenografts

    Anticancer combination therapy has been developed to increase efficacy by enhancing synergy. Patient-derived xenografts (PDXs) have emerged as reliable preclinical models to develop effective treatments in tra...

    Licai Huang, **g Wang, Bingliang Fang, Funda Meric-Bernstam in Scientific Reports (2022)

  4. Article

    Open Access

    Combined MEK/MDM2 inhibition demonstrates antitumor efficacy in TP53 wild-type thyroid and colorectal cancers with MAPK alterations

    Most tumors with activating MAPK (mitogen-activated protein kinase) pathway alterations respond poorly to MEK inhibitors alone. Here, we evaluated combination therapy with MEK inhibitor selumetinib and MDM2 in...

    Seyed Pairawan, Argun Akcakanat, Scott Kopetz, Coya Tapia in Scientific Reports (2022)

  5. Article

    Open Access

    Author Correction: Comprehensive characterization of 536 patient-derived xenograft models prioritizes candidates for targeted treatment

    Hua Sun, Song Cao, R. Jay Mashl, Chia-Kuei Mo, Simone Zaccaria in Nature Communications (2022)

  6. Article

    Open Access

    Structure-based classification predicts drug response in EGFR-mutant NSCLC

    Epidermal growth factor receptor (EGFR) mutations typically occur in exons 18–21 and are established driver mutations in non-small cell lung cancer (NSCLC)13. Targeted therapies are approved for patients with ‘c...

    Jacqulyne P. Robichaux, **uning Le, R. S. K. Vijayan, J. Kevin Hicks, Simon Heeke in Nature (2021)

  7. Article

    Open Access

    Comprehensive characterization of 536 patient-derived xenograft models prioritizes candidates for targeted treatment

    Development of candidate cancer treatments is a resource-intensive process, with the research community continuing to investigate options beyond static genomic characterization. Toward this goal, we have estab...

    Hua Sun, Song Cao, R. Jay Mashl, Chia-Kuei Mo, Simone Zaccaria in Nature Communications (2021)

  8. Article

    Author Correction: DHODH-mediated ferroptosis defence is a targetable vulnerability in cancer

    Chao Mao, **aoguang Liu, Yilei Zhang, Guang Lei, Yuelong Yan, Hyemin Lee in Nature (2021)

  9. Article

    Open Access

    Author Correction: Conservation of copy number profiles during engraftment and passaging of patient-derived cancer xenografts

    A Correction to this paper has been published: https://doi.org/10.1038/s41588-021-00811-4.

    **ng Yi Woo, Jessica Giordano, Anuj Srivastava, Zi-Ming Zhao in Nature Genetics (2021)

  10. Article

    Open Access

    mTORC1 couples cyst(e)ine availability with GPX4 protein synthesis and ferroptosis regulation

    Glutathione peroxidase 4 (GPX4) utilizes glutathione (GSH) to detoxify lipid peroxidation and plays an essential role in inhibiting ferroptosis. As a selenoprotein, GPX4 protein synthesis is highly inefficient...

    Yilei Zhang, Robert V. Swanda, Litong Nie, **aoguang Liu in Nature Communications (2021)

  11. Article

    Open Access

    Conservation of copy number profiles during engraftment and passaging of patient-derived cancer xenografts

    Patient-derived xenografts (PDXs) are resected human tumors engrafted into mice for preclinical studies and therapeutic testing. It has been proposed that the mouse host affects tumor evolution during PDX engr...

    **ng Yi Woo, Jessica Giordano, Anuj Srivastava, Zi-Ming Zhao in Nature Genetics (2021)

  12. Article

    Open Access

    Therapeutic targeting of the PI4K2A/PKR lysosome network is critical for misfolded protein clearance and survival in cancer cells

    The role of RNA-dependent protein kinase R (PKR) and its association with misfolded protein expression in cancer cells are unclear. Herein we report that PKR regulates misfolded protein clearance by preventing...

    Apar Pataer, Bulent Ozpolat, Ru** Shao, Neil R. Cashman, Steven S. Plotkin in Oncogene (2020)

  13. Article

    Open Access

    Repurposing auranofin to treat TP53-mutated or PTEN-deleted refractory B-cell lymphoma

    Jeffrey Wang, Jacqueline Wang, Elyse Lopez, Hui Guo, Hui Zhang in Blood Cancer Journal (2019)

  14. Article

    Open Access

    Patient-derived tumor immune microenvironments in patient-derived xenografts of lung cancer

    Because patient-derived xenografts (PDXs) are grown in immunodeficient mouse strains, PDXs are regarded as lacking an immune microenvironment. However, whether patients’ immune cells co-exist in PDXs remains u...

    **ngxiang Pu, Ran Zhang, Li Wang, Yungchang Chen in Journal of Translational Medicine (2018)

  15. Article

    Open Access

    Immunotherapy for non-small cell lung cancers: biomarkers for predicting responses and strategies to overcome resistance

    Recent breakthroughs in targeted therapy and immunotherapy have revolutionized the treatment of lung cancer, the leading cause of cancer-related deaths in the United States and worldwide. Here we provide an ov...

    **ngxiang Pu, Lin Wu, Dan Su, Weimin Mao, Bingliang Fang in BMC Cancer (2018)

  16. Article

    Author Correction: Mutations in the SWI/SNF complex induce a targetable dependence on oxidative phosphorylation in lung cancer

    In the version of this article originally published, information regarding several funding sources was omitted from the Acknowledgements section. The following sentences should have been included: “This work w...

    Yonathan Lissanu Deribe, Yuting Sun, Christopher Terranova, Fatima Khan in Nature Medicine (2018)

  17. Article

    Open Access

    TUSC2(FUS1)-erlotinib Induced Vulnerabilities in Epidermal Growth Factor Receptor(EGFR) Wildtype Non-small Cell Lung Cancer(NSCLC) Targeted by the Repurposed Drug Auranofin

    Expression of the TUSC2/FUS1 tumor suppressor gene in TUSC2 deficient EGFR wildtype lung cancer cells increased sensitivity to erlotinib. Microarray mRNA expression analysis of TUSC2 inducible lung cancer cell...

    Cao **aobo, Mourad Majidi, Meng Feng, Ru** Shao, **g Wang in Scientific Reports (2016)

  18. Article

    Open Access

    Predictive biomarkers in precision medicine and drug development against lung cancer

    The molecular characterization of various cancers has shown that cancers with the same origins, histopathologic diagnoses, and clinical stages can be highly heterogeneous in their genetic and epigenetic altera...

    Bingliang Fang, Reza J Mehran, John V Heymach in Chinese Journal of Cancer (2015)

  19. Article

    Open Access

    Elafin, an inhibitor of elastase, is a prognostic indicator in breast cancer

    Elafin is an elastase-specific inhibitor with increased transcription in normal mammary epithelial cells compared to mammary carcinoma cells. In this report, we test the hypothesis that inhibition of elastase,...

    Kelly K Hunt, Hannah Wingate, Tomoya Yokota, Yanna Liu in Breast Cancer Research (2013)

  20. Article

    Open Access

    Targeting different types of human meningioma and glioma cells using a novel adenoviral vector expressing GFP-TRAIL fusion protein from hTERT promoter

    The objective of this study was to evaluate the anti-tumor effects of Ad/gTRAIL (an adenoviral vector in which expression of GFP and TRAIL is driven by a human telomerase reverse transcriptase promoter, hTERT)...

    Jessica T Li, Ka Bian, Alan L Zhang, Dong H Kim in Cancer Cell International (2011)

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