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Xinying Yang
Researcher at Chinese Academy of Sciences
Publications - 20
Citations - 620
Xinying Yang is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Cancer & PARP inhibitor. The author has an hindex of 13, co-authored 19 publications receiving 479 citations.
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Journal ArticleDOI
Feedback Activation of Leukemia Inhibitory Factor Receptor Limits Response to Histone Deacetylase Inhibitors in Breast Cancer
Hanlin Zeng,Jia Qu,Nan Jin,Jun Xu,Chenchu Lin,Yi Chen,Xinying Yang,Xiang He,Shuai Tang,Lan Xiaojing,Xiao-Tong Yang,Ziqi Chen,Min Huang,Jian Ding,Meiyu Geng +14 more
TL;DR: It is discovered that feedback activation of leukemia inhibitory factor receptor (LIFR) signaling in breast cancer limits the response to HDAC inhibition, implicating combination inhibition of HDAC with JAK1 or BRD4 as potential therapies for breast cancer.
Journal ArticleDOI
Phosphoglycerate mutase 1 promotes cancer cell migration independent of its metabolic activity.
Di Zhang,Nan Jin,Wei Sun,Xia Li,Bo Liu,Zuoquan Xie,Jia Qu,Jiangshan Xu,Xinying Yang,Yi Su,Shuang Tang,H Han,Dong-Ying Chen,Jian Ding,Minjia Tan,Min Huang,Meiyu Geng +16 more
TL;DR: This study provided the first evidence revealing a non-metabolic function of PGAM1 in promoting cell migration, and gained new insights into the role of PG AM1 in cancer progression.
Journal ArticleDOI
Evaluating the possibility of using acetone‐butanol‐ethanol (ABE) fermentation wastewater for bacterial cellulose production by Gluconacetobacter xylinus
Chao Huang,Xinying Yang,Lian Xiong,Hai Jun Guo,Jing Luo,Bo Wang,Haijuan Zhang,Lin Xiaoqing,Chen Xuefang +8 more
TL;DR: ABE fermentation wastewater is one promising substrate for BC production and showed small influence on the BC structure by comparison with the BC products obtained in traditional HS medium using field emission scanning electron microscope (FE‐SEM), Fourier transform infrared spectroscopy (FTIR) and X‐ray diffraction (XRD).
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Discovery of 3-(5'-Substituted)-Benzimidazole-5-(1-(3,5-dichloropyridin-4-yl)ethoxy)-1H-indazoles as Potent Fibroblast Growth Factor Receptor Inhibitors: Design, Synthesis, and Biological Evaluation.
Wei Yan,Wang Xinyi,Yang Dai,Bin Zhao,Xinying Yang,Jun Fan,Yinglei Gao,Fanwang Meng,Fanwang Meng,Yuming Wang,Cheng Luo,Jing Ai,Meiyu Geng,Wenhu Duan,Wenhu Duan +14 more
TL;DR: The identification of the potent pan-FGFR inhibitor (R)-21c is described, which provided nearly complete inhibition of tumor growth in NCI-H1581 (FGFR1-amplified) xenograft mice model at the dose of 10 mg/kg/qd via oral administration.
Journal ArticleDOI
c-Myc Alterations Confer Therapeutic Response and Acquired Resistance to c-Met Inhibitors in MET-Addicted Cancers
Aijun Shen,Lu Wang,Min Huang,J.R. Sun,Yi Chen,Yanyan Shen,Xinying Yang,Xin Wang,Jian Ding,Meiyu Geng +9 more
TL;DR: It is reported that the transcriptional factor c-Myc functions as a downstream effector to dictate the therapeutic response to c-Met inhibitors in c- Met-addicted cancer and derived resistance, offering a preclinical proof of concept for the application of c- myc-blocking agents as a tactic to thwart resistance to kinase inhibitors.