Q
Qiang Xia
Researcher at Shanghai Jiao Tong University
Publications - 284
Citations - 5334
Qiang Xia is an academic researcher from Shanghai Jiao Tong University. The author has contributed to research in topics: Liver transplantation & Medicine. The author has an hindex of 33, co-authored 223 publications receiving 3507 citations.
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Journal ArticleDOI
YTHDF2 reduction fuels inflammation and vascular abnormalization in hepatocellular carcinoma.
Jiajie Hou,He Zhang,He Zhang,Jun Liu,Zhenjun Zhao,Jianye Wang,Zhike Lu,Bian Hu,Jiankui Zhou,Zhicong Zhao,Mingxuan Feng,Haiyan Zhang,Haiyan Zhang,Bin Shen,Xingxu Huang,Beicheng Sun,Chuan He,Chuan He,Qiang Xia +18 more
TL;DR: The results have characterized the m6A-mRNA landscape in human HCC and revealed YTHDF2 as a molecular ‘rheostat’ in epitranscriptome and cancer progression.
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Cisplatin-induced downregulation of miR-199a-5p increases drug resistance by activating autophagy in HCC cell
TL;DR: It is found that miR-199a-5p levels were significantly reduced in HCC patients treated with cisplatin-based chemotherapy, thus offering a new target for chemotherapy of HCC.
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The Role of Nrf2 in Liver Disease: Novel Molecular Mechanisms and Therapeutic Approaches.
TL;DR: Recent advances in the function and principal mechanisms by regulating Nrf2 in liver diseases, including acute liver failure, hepatic ischemia–reperfusion injury (IRI), alcoholic liver disease, viral hepatitis, non-alcoholic fatty liver disease (NAFLD), non- alcoholic steatohepatitis (NASH), and hepatocellular carcinoma are discussed.
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Exosome-mediated secretion of LOXL4 promotes hepatocellular carcinoma cell invasion and metastasis.
Rong-Kun Li,Ya-Hui Wang,Xiao-Xin Zhang,Mingxuan Feng,Jun Ma,Jun Li,Xiao-Mei Yang,Fang Fang,Qiang Xia,Zhigang Zhang,Mingyi Shang,Shu-Heng Jiang +11 more
TL;DR: A novel function of LOXL4 in tumor metastasis mediated by exosomes through regulation of the FAK/Src pathway and angiogenesis in HCC is demonstrated.
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Upregulated miR-130a increases drug resistance by regulating RUNX3 and Wnt signaling in cisplatin-treated HCC cell.
TL;DR: It is demonstrated that upregulated miR-130a directly inhibited expression of tumor suppressor gene RUNX3, which resulted in activation of Wnt/β-catenin signaling and increased drug resistance, thus offering a new target for chemotherapy of HCC.