Suchergebnisse - "Jiang, Baishan"
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USP8 inhibition reshapes an inflamed tumor microenvironment that potentiates the immunotherapy
ISSN: 2041-1723, 2041-1723Veröffentlicht: London Nature Publishing Group UK 31.03.2022Veröffentlicht in Nature communications (31.03.2022)“… Anti-PD-1/PD-L1 immunotherapy has achieved impressive therapeutic outcomes in patients with multiple cancer types. However, the underlined molecular …”
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Discovery and resistance mechanism of a selective CDK12 degrader
ISSN: 1552-4450, 1552-4469, 1552-4469Veröffentlicht: New York Nature Publishing Group US 01.06.2021Veröffentlicht in Nature chemical biology (01.06.2021)“… Cyclin-dependent kinase 12 (CDK12) is an emerging therapeutic target due to its role in regulating transcription of DNA-damage response (DDR) genes. However, …”
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Pharmacological perturbation of CDK9 using selective CDK9 inhibition or degradation
ISSN: 1552-4450, 1552-4469, 1552-4469Veröffentlicht: United States Nature Publishing Group 01.02.2018Veröffentlicht in Nature chemical biology (01.02.2018)“… Cyclin-dependent kinase 9 (CDK9), an important regulator of transcriptional elongation, is a promising target for cancer therapy, particularly for cancers …”
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Homolog-Selective Degradation as a Strategy to Probe the Function of CDK6 in AML
ISSN: 2451-9448, 2451-9448Veröffentlicht: United States 21.02.2019Veröffentlicht in Cell chemical biology (21.02.2019)“… The design of selective small molecules is often stymied by similar ligand binding pockets. Here, we report BSJ-03-123, a phthalimide-based degrader that …”
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INK4 Tumor Suppressor Proteins Mediate Resistance to CDK4/6 Kinase Inhibitors
ISSN: 2159-8290, 2159-8290Veröffentlicht: United States 01.02.2022Veröffentlicht in Cancer discovery (01.02.2022)“… Cyclin-dependent kinases 4 and 6 (CDK4/6) represent a major therapeutic vulnerability for breast cancer. The kinases are clinically targeted via ATP …”
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MELK is not necessary for the proliferation of basal-like breast cancer cells
ISSN: 2050-084X, 2050-084XVeröffentlicht: England eLife Sciences Publications Ltd 19.09.2017Veröffentlicht in eLife (19.09.2017)“… Thorough preclinical target validation is essential for the success of drug discovery efforts. In this study, we combined chemical and genetic perturbants, …”
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Therapeutic targeting nudix hydrolase 1 creates a MYC-driven metabolic vulnerability
ISSN: 2041-1723, 2041-1723Veröffentlicht: London Nature Publishing Group UK 16.03.2024Veröffentlicht in Nature communications (16.03.2024)“… Tumor cells must rewire nucleotide synthesis to satisfy the demands of unbridled proliferation. Meanwhile, they exhibit augmented reactive oxygen species (ROS) …”
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Catalytic Degraders Effectively Address Kinase Site Mutations in EML4-ALK Oncogenic Fusions
ISSN: 1520-4804, 1520-4804Veröffentlicht: United States 27.04.2023Veröffentlicht in Journal of medicinal chemistry (27.04.2023)“… Heterobifunctional degraders, known as proteolysis targeting chimeras (PROTACs), theoretically possess a catalytic mode-of-action, yet few studies have either …”
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Palmitoylation of KSHV pORF55 is required for Golgi localization and efficient progeny virion production
ISSN: 1553-7374, 1553-7366, 1553-7374Veröffentlicht: United States Public Library of Science 01.04.2024Veröffentlicht in PLoS pathogens (01.04.2024)“… Kaposi’s sarcoma-associated herpesvirus (KSHV) is a double-stranded DNA virus etiologically associated with multiple malignancies. Both latency and sporadic …”
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Ligase IV inhibitor SCR7 enhances gene editing directed by CRISPR–Cas9 and ssODN in human cancer cells
ISSN: 2045-3701, 2045-3701Veröffentlicht: London BioMed Central 19.02.2018Veröffentlicht in Cell & bioscience (19.02.2018)“… Background Precise genome editing is essential for both basic and translational research. The recently developed CRISPR/Cas9 system can specifically cleave a …”
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ULK1 inhibition overcomes compromised antigen presentation and restores antitumor immunity in LKB1-mutant lung cancer
ISSN: 2662-1347, 2662-1347Veröffentlicht: England Nature Publishing Group 01.05.2021Veröffentlicht in Nature cancer (01.05.2021)“… Inactivating mutations in LKB1/STK11 are present in roughly 20% of nonsmall cell lung cancers (NSCLC) and portend poor response to anti-PD-1 immunotherapy …”
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Targeting protein tyrosine phosphatases for CDK6-induced immunotherapy resistance
ISSN: 2211-1247, 2211-1247Veröffentlicht: United States Elsevier Inc 25.04.2023Veröffentlicht in Cell reports (Cambridge) (25.04.2023)“… Elucidating the mechanisms of resistance to immunotherapy and developing strategies to improve its efficacy are challenging goals. Bioinformatics analysis …”
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Increased lysosomal biomass is responsible for the resistance of triple-negative breast cancers to CDK4/6 inhibition
ISSN: 2375-2548, 2375-2548Veröffentlicht: United States American Association for the Advancement of Science 01.06.2020Veröffentlicht in Science advances (01.06.2020)“… This study presents strategies to render triple-negative breast cancers sensitive to CDK4/6 inhibitors. Inhibitors of cyclin-dependent kinases CDK4 and CDK6 …”
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Development of Oral, Potent, and Selective CK1α Degraders for AML Therapy
ISSN: 2691-3704, 2691-3704Veröffentlicht: United States American Chemical Society 25.11.2024Veröffentlicht in JACS Au (25.11.2024)“… Molecular glue degraders (MGDs) are proximity-inducing agents that mediate the cooperative interaction between a target protein and an E3 ligase, introducing …”
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ELISA detection of semicarbazide based on a fast sample pretreatment method
ISSN: 1359-7345, 1364-548X, 1364-548XVeröffentlicht: CAMBRIDGE Royal Soc Chemistry 01.01.2013Veröffentlicht in Chemical communications (Cambridge, England) (01.01.2013)“… A direct ELISA was established for the fast detection of semicarbazide (SEM) using a novel biotin derivative. Without a tedious extraction procedure, as low as …”
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Harmine Induces Adipocyte Thermogenesis through RAC1-MEK-ERK-CHD4 Axis
ISSN: 2045-2322, 2045-2322Veröffentlicht: London Nature Publishing Group UK 02.11.2016Veröffentlicht in Scientific reports (02.11.2016)“… Harmine is a natural compound possessing insulin-sensitizing effect in db/db diabetic mice. However its effect on adipose tissue browning is unknown. Here we …”
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Development of Dual and Selective Degraders of Cyclin‐Dependent Kinases 4 and 6
ISSN: 1433-7851, 1521-3773, 1521-3773Veröffentlicht: WEINHEIM Wiley 06.05.2019Veröffentlicht in Angewandte Chemie International Edition (06.05.2019)“… Cyclin‐dependent kinases 4 and 6 (CDK4/6) are key regulators of the cell cycle, and there are FDA‐approved CDK4/6 inhibitors for treating patients with …”
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Mapping the Degradable Kinome Provides a Resource for Expedited Degrader Development
ISSN: 1097-4172, 1097-4172Veröffentlicht: United States 10.12.2020Veröffentlicht in Cell (10.12.2020)“… Targeted protein degradation (TPD) refers to the use of small molecules to induce ubiquitin-dependent degradation of proteins. TPD is of interest in drug …”
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Selective and Potent Molecular Glue Degraders for NIMA‐Related Kinase 7
ISSN: 1433-7851, 1521-3773, 1521-3773Veröffentlicht: WEINHEIM Wiley 17.03.2025Veröffentlicht in Angewandte Chemie International Edition (17.03.2025)“… Molecular glue degraders (MGDs) represent a promising strategy for targeted protein degradation within cells. While chemoproteomics has unveiled hundreds of …”
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PROTAC-mediated CDK degradation differentially impacts cancer cell cycles due to heterogeneity in kinase dependencies
ISSN: 0007-0920, 1532-1827, 1532-1827Veröffentlicht: England Nature Publishing Group 12.10.2023Veröffentlicht in British journal of cancer (12.10.2023)“… Cyclin-dependent kinase 4 and 6 (CDK4/6) inhibition yields differential cellular responses in multiple tumor models due to redundancy in cell cycle. We …”
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