Albumin-based drug carrier targeting urokinase receptor for cancer therapy.
暂无分享,去创建一个
C. Yuan | Mingdong Huang | Yang Zhou | Peng Xu | Shujuan Yu | Longguang Jiang | Hanlin Li | Shanli Chen | Yuhan Qu | Zhiyou Wang
[1] B. Ghosh,et al. Human serum albumin-poly(Lactide)-conjugated self-assembly NPs for targeted docetaxel delivery and improved therapeutic efficacy in oral cancer. , 2022, International journal of biological macromolecules.
[2] C. Yuan,et al. A versatile insertion point on albumin to accommodate peptides and maintain their activities. , 2022, International journal of biological macromolecules.
[3] B. Ghosh,et al. Oleanolic Acid-conjugated human serum albumin nanoparticles encapsulating doxorubicin as synergistic combination chemotherapy in oropharyngeal carcinoma and melanoma. , 2022, International journal of pharmaceutics.
[4] M. Ploug,et al. The Urokinase Receptor (uPAR) as a “Trojan Horse” in Targeted Cancer Therapy: Challenges and Opportunities , 2021, Cancers.
[5] Y. Zhen,et al. The development of human serum albumin-based drugs and relevant fusion proteins for cancer therapy. , 2021, International journal of biological macromolecules.
[6] Jakob Nikolas Kather,et al. Serum Levels of Soluble Urokinase Plasminogen Activator Receptor Predict Tumor Response and Outcome to Immune Checkpoint Inhibitor Therapy , 2021, Frontiers in Oncology.
[7] C. Yuan,et al. Development of inhibitors for uPAR: blocking the interaction of uPAR with its partners. , 2021, Drug discovery today.
[8] M. Otagiri,et al. Serum Albumin, Lipid and Drug Binding. , 2020, Sub-cellular biochemistry.
[9] Wei Gao,et al. Correction to: Celastrol mediates autophagy and apoptosis via the ROS/JNK and Akt/mTOR signaling pathways in glioma cells , 2019, Journal of experimental & clinical cancer research : CR.
[10] G. Rabbani,et al. Structure, enzymatic activities, glycation and therapeutic potential of human serum albumin: A natural cargo. , 2019, International journal of biological macromolecules.
[11] Chern Ein Oon,et al. Molecular targeted therapy: Treating cancer with specificity , 2018, European journal of pharmacology.
[12] J. Zhao,et al. A Mechanistic Overview of Triptolide and Celastrol, Natural Products from Tripterygium wilfordii Hook F , 2018, Front. Pharmacol..
[13] O. Abdallah,et al. Self-assembled phospholipid-based phytosomal nanocarriers as promising platforms for improving oral bioavailability of the anticancer celastrol. , 2018, International journal of pharmaceutics.
[14] Chen Jiang,et al. Biomacromolecules as carriers in drug delivery and tissue engineering , 2017, Acta pharmaceutica Sinica. B.
[15] J. Fonseca,et al. Celastrol: A Spectrum of Treatment Opportunities in Chronic Diseases , 2017, Front. Med..
[16] X. Miao,et al. Celastrol inhibits chondrosarcoma proliferation, migration and invasion through suppression CIP2A/c-MYC signaling pathway. , 2017, Journal of pharmacological sciences.
[17] C. H. Nielsen,et al. First-in-human uPAR PET: Imaging of Cancer Aggressiveness , 2015, Theranostics.
[18] C. Yuan,et al. A drug carrier targeting murine uPAR for photodynamic therapy and tumor imaging. , 2015, Acta biomaterialia.
[19] W. Strohl. Fusion Proteins for Half-Life Extension of Biologics as a Strategy to Make Biobetters , 2015, BioDrugs.
[20] Yunmei Huang,et al. Zinc phthalocyanine conjugated with the amino-terminal fragment of urokinase for tumor-targeting photodynamic therapy. , 2014, Acta biomaterialia.
[21] Xiaole Qi,et al. Solid self-microemulsifying dispersible tablets of celastrol: formulation development, charaterization and bioavailability evaluation. , 2014, International journal of pharmaceutics.
[22] S. Lippard,et al. Pt(IV) Prodrugs Designed to Bind Non-Covalently to Human Serum Albumin for Drug Delivery , 2014, Journal of the American Chemical Society.
[23] H. Nielsen,et al. Urokinase-type plasminogen activator receptor (uPAR) on tumor-associated macrophages is a marker of poor prognosis in colorectal cancer , 2014, Cancer medicine.
[24] Guang-Biao Zhou,et al. Cancerous inhibitor of PP2A is targeted by natural compound celastrol for degradation in non-small-cell lung cancer. , 2014, Carcinogenesis.
[25] Wei Zheng,et al. A Novel Tumor Targeting Drug Carrier for Optical Imaging and Therapy , 2014, Theranostics.
[26] Yaping Wang,et al. Comparative Study of Somatostatin-Human Serum Albumin Fusion Proteins and Natural Somatostatin on Receptor Binding, Internalization and Activation , 2014, PloS one.
[27] Leslie R Evans,et al. Albumin as a versatile platform for drug half-life extension. , 2013, Biochimica et biophysica acta.
[28] Sang Mee Lee,et al. Novel AGLP-1 albumin fusion protein as a long-lasting agent for type 2 diabetes , 2013, BMB reports.
[29] Shuang Huang,et al. Role of Urokinase Receptor in Tumor Progression and Development , 2013, Theranostics.
[30] A. Kjaer,et al. Urokinase-type plasminogen activator receptor (uPAR) as a promising new imaging target: potential clinical applications , 2013, Clinical physiology and functional imaging.
[31] Mingdong Huang,et al. Structure-based Engineering of Species Selectivity in the Interaction between Urokinase and Its Receptor , 2010, The Journal of Biological Chemistry.
[32] C. Marshall,et al. Regulation of cell signalling by uPAR , 2010, Nature Reviews Molecular Cell Biology.
[33] Paula D. Bos,et al. Metastasis: from dissemination to organ-specific colonization , 2009, Nature Reviews Cancer.
[34] Mingdong Huang,et al. A new drug binding subsite on human serum albumin and drug-drug interaction studied by X-ray crystallography. , 2008, Journal of structural biology.
[35] Craig M. Crews,et al. Molecular Understanding and Modern Application of Traditional Medicines: Triumphs and Trials , 2007, Cell.
[36] Patrick Soon-Shiong,et al. Increased antitumor activity, intratumor paclitaxel concentrations, and endothelial cell transport of cremophor-free, albumin-bound paclitaxel, ABI-007, compared with cremophor-based paclitaxel. , 2006, Clinical cancer research : an official journal of the American Association for Cancer Research.
[37] S. Curry,et al. Structural basis of the drug-binding specificity of human serum albumin. , 2005, Journal of molecular biology.
[38] A. Ménez,et al. Crystal structure of the human urokinase plasminogen activator receptor bound to an antagonist peptide , 2005, The EMBO journal.
[39] C. D. de Bock,et al. Clinical significance of urokinase‐type plasminogen activator receptor (uPAR) expression in cancer , 2004, Medicinal research reviews.
[40] N. Schmiedeberg,et al. Synthesis, solution structure, and biological evaluation of urokinase type plasminogen activator (uPA)-derived receptor binding domain mimetics. , 2002, Journal of medicinal chemistry.
[41] W. Hall,et al. Targeting urokinase-type plasminogen activator receptor on human glioblastoma tumors with diphtheria toxin fusion protein DTAT. , 2002, Journal of the National Cancer Institute.
[42] M. Ploug,et al. Peptide-derived antagonists of the urokinase receptor. affinity maturation by combinatorial chemistry, identification of functional epitopes, and inhibitory effect on cancer cell intravasation. , 2001, Biochemistry.
[43] S. Curry,et al. Crystallographic analysis reveals common modes of binding of medium and long-chain fatty acids to human serum albumin. , 2000, Journal of molecular biology.
[44] D. Hanahan,et al. The Hallmarks of Cancer , 2000, Cell.