A modified natural small molecule inhibits triple-negative breast cancer growth by interacting with Tubb3
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T. Yin | Yonghua Yang | Zhongling Wen | Minkai Yang | Xiaoming Wang | Jinliang Qi | Hongyan Lin | R. Fang | Xiaorong Yang | Hongyuan Chen | Xiaohui Lai | Xuan Wang | Yahan Zhang | Quan Zhao | H. Han
[1] Y. Kong,et al. The Single‐Cell Landscape of Intratumoral Heterogeneity and The Immunosuppressive Microenvironment in Liver and Brain Metastases of Breast Cancer , 2022, Advanced science.
[2] Hailin Tang,et al. The FUS/circEZH2/KLF5/ feedback loop contributes to CXCR4-induced liver metastasis of breast cancer by enhancing epithelial-mesenchymal transition , 2022, Molecular Cancer.
[3] Wanzi Yao,et al. Advances in anti-cancer effects and underlying mechanisms of marine algae polysaccharides. , 2022, International journal of biological macromolecules.
[4] A. Jemal,et al. Cancer treatment and survivorship statistics, 2022 , 2022, CA: a cancer journal for clinicians.
[5] P. K. Naik,et al. In vitro characterization and molecular dynamic simulation of shikonin as a tubulin-targeted anticancer agent , 2022, Comput. Biol. Medicine.
[6] R. Aebersold,et al. SWATH-MS Analysis of FFPE Tissues Identifies Stathmin as a Potential Marker of Endometrial Cancer in Patients Exposed to Tamoxifen. , 2020, Journal of proteome research.
[7] L. Cai,et al. Targeting the IL-1β/EHD1/TUBB3 axis overcomes resistance to EGFR-TKI in NSCLC , 2019, Oncogene.
[8] D. Xie,et al. LncRNA RPPH1 promotes colorectal cancer metastasis by interacting with TUBB3 and by promoting exosomes-mediated macrophage M2 polarization , 2019, Cell Death & Disease.
[9] T. Efferth,et al. Shikonin derivatives for cancer prevention and therapy. , 2019, Cancer letters.
[10] A. Fernández-Carballido,et al. Current status of nanomedicine in the chemotherapy of breast cancer , 2019, Cancer Chemotherapy and Pharmacology.
[11] M. Yar,et al. Anti-tubulin agents of natural origin: Targeting taxol, vinca, and colchicine binding domains. , 2019, European journal of medicinal chemistry.
[12] Q. Gao,et al. Shikonin inhibits cancer cell cycling by targeting Cdc25s , 2019, BMC Cancer.
[13] K. Zen,et al. Shikonin Inhibits Tumor Growth in Mice by Suppressing Pyruvate Kinase M2-mediated Aerobic Glycolysis , 2018, Scientific Reports.
[14] P. Clarke,et al. Atypical APC/C‐dependent degradation of Mcl‐1 provides an apoptotic timer during mitotic arrest , 2018, The EMBO journal.
[15] Yong-Hua Yang,et al. Design and characterization of α-lipoic acyl shikonin ester twin drugs as tubulin and PDK1 dual inhibitors. , 2018, European journal of medicinal chemistry.
[16] Peng-Fei Wang,et al. Identification of new shikonin derivatives as STAT3 inhibitors , 2017, Biochemical pharmacology.
[17] H. Kuwano,et al. High STMN1 Expression is Associated with Cancer Progression and Chemo-Resistance in Lung Squamous Cell Carcinoma , 2017, Annals of Surgical Oncology.
[18] Tianhua Zhou,et al. Microtubule-binding protein FOR20 promotes microtubule depolymerization and cell migration , 2017, Cell Discovery.
[19] Rong Liu,et al. YD277 Suppresses Triple-Negative Breast Cancer Partially Through Activating the Endoplasmic Reticulum Stress Pathway , 2017, Theranostics.
[20] Y. Liu,et al. Suppression of PTEN/AKT signaling decreases the expression of TUBB3 and TOP2A with subsequent inhibition of cell growth and induction of apoptosis in human breast cancer MCF-7 cells via ATP and caspase-3 signaling pathways. , 2017, Oncology reports.
[21] Zhenzhong Zhu,et al. Exosomes derived from human platelet-rich plasma prevent apoptosis induced by glucocorticoid-associated endoplasmic reticulum stress in rat osteonecrosis of the femoral head via the Akt/Bad/Bcl-2 signal pathway , 2017, Theranostics.
[22] J. Balko,et al. Triple-negative breast cancer: challenges and opportunities of a heterogeneous disease , 2016, Nature Reviews Clinical Oncology.
[23] Gary D Bader,et al. Functional Genomic Landscape of Human Breast Cancer Drivers, Vulnerabilities, and Resistance , 2016, Cell.
[24] Haw‐Wen Chen,et al. Shikonin inhibits oxidized LDL-induced monocyte adhesion by suppressing NFκB activation via up-regulation of PI3K/Akt/Nrf2-dependent antioxidation in EA.hy926 endothelial cells. , 2015, Biochemical pharmacology.
[25] M. Kavallaris,et al. TUBB3/βIII-tubulin acts through the PTEN/AKT signaling axis to promote tumorigenesis and anoikis resistance in non-small cell lung cancer. , 2015, Cancer research.
[26] A. Letai,et al. APC(Cdc20) suppresses apoptosis through targeting Bim for ubiquitination and destruction. , 2014, Developmental cell.
[27] P Kronqvist,et al. Cdc20 and securin overexpression predict short-term breast cancer survival , 2014, British Journal of Cancer.
[28] M. Kavallaris,et al. Microtubule Dynamics, Mitotic Arrest, and Apoptosis: Drug-Induced Differential Effects of βIII-Tubulin , 2010, Molecular Cancer Therapeutics.
[29] S. Ellard,et al. A phase IB study of ABT-751 in combination with docetaxel in patients with advanced castration-resistant prostate cancer. , 2010, Annals of oncology : official journal of the European Society for Medical Oncology.
[30] S. Geley,et al. Dose‐dependent effects of stable cyclin B1 on progression through mitosis in human cells , 2006, The EMBO journal.
[31] E. Martinelli,et al. Class III β-Tubulin Overexpression Is a Marker of Poor Clinical Outcome in Advanced Ovarian Cancer Patients , 2006, Clinical Cancer Research.
[32] D. Sackett,et al. Localization of the colchicine-binding site of tubulin. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[33] M. Gayyed,et al. A comprehensive analysis of CDC20 overexpression in common malignant tumors from multiple organs: its correlation with tumor grade and stage , 2015, Tumor Biology.