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Research Paper - Translational
HMGB1 represses the anti-cancer activity of sunitinib by governing TP53 autophagic degradation via its nucleus-to-cytoplasm transport
Peihua LuoInstitute of Pharmacology & Toxicology, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, ChinaCorrespondence[email protected] [email protected] [email protected]
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Zhifei XuInstitute of Pharmacology & Toxicology, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, ChinaView further author information
, Guanqun LiInstitute of Pharmacology & Toxicology, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, ChinaView further author information
, Hao YanInstitute of Pharmacology & Toxicology, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, ChinaView further author information
, Yi ZhuInstitute of Pharmacology & Toxicology, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, ChinaView further author information
, Hong ZhuInstitute of Pharmacology & Toxicology, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, ChinaView further author information
, Shenglin MaDepartment of Oncology, Hangzhou First People’s Hospital, Nanjing Medical University, Hangzhou, ChinaView further author information
, Bo YangInstitute of Pharmacology & Toxicology, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, ChinaCorrespondence[email protected] [email protected] [email protected]
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Qiaojun HeInstitute of Pharmacology & Toxicology, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, ChinaCorrespondence[email protected] [email protected] [email protected]
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show allView further author information
Pages 2155-2170
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Received 05 Sep 2017, Accepted 10 Jul 2018, Published online: 11 Sep 2018
Related Research Data
HMGB1 represses the anti-cancer activity of sunitinib by governing TP53 autophagic degradation via its nucleus-to-cytoplasm transport
Source:
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HMGB1 represses the anti-cancer activity of sunitinib by governing TP53 autophagic degradation via its nucleus-to-cytoplasm transport.
Source:
Taylor & Francis
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