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许秋然 封面图

许秋然|Qiuran Xu

hangzhou medical college邮箱:xuqiuran@hmc.edu.cn
H指数:37
被引数:4,621
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个人简介

"许秋然,博士,研究员/副主任医师,博士生导师。全省肿瘤分子诊断与个体化治疗研究重点实验室副主任、消化道肿瘤诊疗与药物研发省工程实验室副主任。省级人才计划领军人才,近年来,以第一或通讯作者发表SCI论文80余篇,包括Nat Commun、Research、Adv Funct Mater、Adv Sci、Mol Ther、Nucleic Acids Res、Mol Cancer、Cancer Lett、J Nanobiotechnology等国内外知名期刊。主持国家自然科学基金2项、省重点研发项目1项、省杰青项目1项、省杰青延续项目1项、省部共建重大项目1项、重点项目1项、中国博士后基金1项、其他省部级项目等5项,参与国家新药创制重大专项等10余项,授权发明专利2项,实用新型专利2项,获浙江省科技进步二等奖4项和浙江省医药科技进步一等奖1项。\n教育背景\n博士:2011 年9 月-2014 年12 月,西安交通大学,外科学(肝胆外科);\n硕士:2004 年9 月-2011 年7 月,西安交通大学,临床医学。\n成果荣誉\n1.2022年,肝胰恶性肿瘤精准诊疗创新技术的基础研究及临床推广应用,浙江省科技进步二等奖,排名2/9;\n2.2020 年,肝癌创新诊疗的基础和临床应用研究,浙江省科技进步二等奖,排名2/9;\n3.2021年,恶性血液病新型诊疗体系和预后模型的建立及应用,浙江省科技进步二等奖,排名4/9;\n4.2016 年,肝胰恶性肿瘤分子标志物与治疗新技术的研究和应用,浙江省科技进步二等奖,排名4/11;\n学术任职\n全省肿瘤分子诊断与个体化治疗研究重点实验室副主任;消化道肿瘤诊疗与药物研发浙江省工程实验室副主任;中华医学会肝病学分会遗传代谢性肝病协作组第一届委员会委员;浙江省医学会常务理事;浙江省医学会分子医学分会常务委员;浙江省医学会科研管理分会常务委员; 《Annals of Translational Medicine》中青年编委;《Journal of Clinical and Translational Hepatology》中青年编委; 《Military Medical Research》期刊中青年编委;《中华肝胆外科手术学电子杂志》中青年编委;《中国普通外科杂志》中青年编委; 《临床与病理杂志》中青年编委。\n主持项目\n1、国家自然科学基金面上项目,缺氧肿瘤微环境中TUFT1促进肝细胞癌生长和转移的机制研究,主持。\n2、国家自然科学基金青年项目,HSP90通过调控PKM2磷酸化促进肝癌细胞糖酵解及增殖侵袭转移的作用机制研究,主持。\n3、浙江省自然科学基金杰出青年基金延续项目,肿瘤细胞双硫死亡的蛋白泛素化修饰调控与靶向治疗研究,主持。\n4、浙江省科技厅领雁项目,恶性肿瘤精准诊治新技术和新策略研究-肝细胞癌新型分子分型及免疫治疗新策略的探索,主持。\n5、浙江省自然科学基金杰出青年项目,去泛素化酶MINDY4作为抗肝癌药物新靶标的可行性和干预研究,主持。\n6、浙江省自然科学基金面上项目,Fbxw7通过泛素化蛋白酶解BCoR-L1蛋白调控肝癌细胞上皮间质转化的机制研究,主持。\n7、浙江省卫健委省部共建重大项目,泛素缀合酶E2K作为抗胃癌药物新靶标的可行性及临床研究,主持。\n8、浙江省医药科技计划省部共建重点项目,长链非编码RNA MCM3AP-AS1作为肝癌诊断新型生物标志物及特异性治疗靶点的研究,主持。\n发表论文\n[1] Q. Xu, C. Yang, Y. Du, Y. Chen, H. Liu, M. Deng, H. Zhang, L. Zhang, T. Liu, Q. Liu, L. Wang, Z. Lou, H. Pei, AMPK regulates histone H2B O-GlcNAcylation, Nucleic Acids Res, 42 (2014) 5594-5604.\n[2] Q. Xu, J. Tu, C. Dou, J. Zhang, L. Yang, X. Liu, K. Lei, Z. Liu, Y. Wang, L. Li, H. Bao, J. Wang, K. Tu, HSP90 promotes cell glycolysis, proliferation and inhibits apoptosis by regulating PKM2 abundance via Thr-328 phosphorylation in hepatocellular carcinoma, Mol Cancer, 16 (2017) 178.\n[3] Y. Wang, L. Yang, T. Chen, X. Liu, Y. Guo, Q. Zhu, X. Tong, W. Yang, Q. Xu, D. Huang, K. Tu, A novel lncRNA MCM3AP-AS1 promotes the growth of hepatocellular carcinoma by targeting miR-194-5p/FOXA1 axis, Mol Cancer, 18 (2019) 28.\n[4] Z. Xiao, Y. Liu, J. Zhao, L. Li, L. Hu, Q. Lu, Z. Zeng, X. Liu, D. Huang, W. Yang, Q. Xu, Long noncoding RNA LINC01123 promotes the proliferation and invasion of hepatocellular carcinoma cells by modulating the miR-34a-5p/TUFT1 axis, Int J Biol Sci, 16 (2020) 2296-2305.\n[5] S. Gao, T. Chen, L. Li, X. Liu, Y. Liu, J. Zhao, Q. Lu, Z. Zeng, Q. Xu, D. Huang, K. Tu, Hypoxia-Inducible Ubiquitin Specific Peptidase 13 Contributes to Tumor Growth and Metastasis via Enhancing the Toll-Like Receptor 4/Myeloid Differentiation Primary Response Gene 88/Nuclear Factor-kappaB Pathway in Hepatocellular Carcinoma, Front Cell Dev Biol, 8 (2020) 587389.\n[6] C. Shen, L. Ding, H. Mo, R. Liu, Q. Xu, K. Tu, Long noncoding RNA FIRRE contributes to the proliferation and glycolysis of hepatocellular carcinoma cells by enhancing PFKFB4 expression, J Cancer, 12 (2021) 4099-4108.\n[7] Z. Zeng, Z. Shi, Y. Liu, J. Zhao, Q. Lu, J. Guo, X. Liu, D. Huang, Q. Xu, HIF-1alpha-activated TM4SF1-AS1 promotes the proliferation, migration, and invasion of hepatocellular carcinoma cells by enhancing TM4SF1 expression, Biochem Biophys Res Commun, 566 (2021) 80-86.\n[8] J. Wang, R. Liu, Y. Wang, H. Mo, Y. Niu, Q. Xu, Q. Liu, Repression of the miR-627-5p by histone deacetylase 3 contributes to hypoxia-induced hepatocellular carcinoma progression, J Cancer, 12 (2021) 5320-5330.\n[9] J. Wang, R. Liu, H. Mo, X. Xiao, Q. Xu, W. Zhao, Deubiquitinase PSMD7 promotes the proliferation, invasion, and cisplatin resistance of gastric cancer cells by stabilizing RAD23B, Int J Biol Sci, 17 (2021) 3331-3342.\n[10] Y. Liu, R. Liu, J. Zhao, Z. Zeng, Z. Shi, Q. Lu, J. Guo, L. Li, Y. Yao, X. Liu, Q. Xu, LncRNA TMEM220-AS1 suppresses hepatocellular carcinoma cell proliferation and invasion by regulating the TMEM220/beta-catenin axis, J Cancer, 12 (2021) 6805-6813.\n[11] Z. Shi, R. Liu, Q. Lu, Z. Zeng, Y. Liu, J. Zhao, X. Liu, L. Li, H. Huang, Y. Yao, D. Huang, Q. Xu, UBE2O promotes hepatocellular carcinoma cell proliferation and invasion by regulating the AMPKalpha2/mTOR pathway, Int J Med Sci, 18 (2021) 3749-3758.\n[12] Y. Ma, X. Qu, C. Liu, Q. Xu, K. Tu, Metal-Organic Frameworks and Their Composites Towards Biomedical Applications, Front Mol Biosci, 8 (2021) 805228.\n[13] M. Yang, C. Yang, Y. Zhang, X. Yan, Y. Ma, Y. Zhang, Y. Cao, Q. Xu, K. Tu, M. Zhang, An oral pH-activated \"nano-bomb\" carrier combined with berberine by regulating gene silencing and gut microbiota for site-specific treatment of ulcerative colitis, Biomater Sci, 10 (2022) 1053-1067.\n[14] K. Fan, Z. Liu, M. Gao, K. Tu, Q. Xu, Y. Zhang, Targeting Nutrient Dependency in Cancer Treatment, Front Oncol, 12 (2022) 820173.\n[15] X. Yan, C. Yang, M. Yang, Y. Ma, Y. Zhang, Y. Zhang, C. Liu, Q. Xu, K. Tu, M. Zhang, All-in-one theranostic nano-platform based on polymer nanoparticles for BRET/FRET-initiated bioluminescence imaging and synergistically anti-inflammatory therapy for ulcerative colitis, J Nanobiotechnology, 20 (2022) 99.\n[16] X. Sun, R.Y. Zhang, F. Zhang, X.L. Hou, K. Cheng, C.Q. Li, X.T. Xie, Z.T. Zhong, B. Zhang, X.Q. Yang, W. Chen, B. Liu, Q.R. Xu, Y.D. Zhao, Multifunctional nanocarrier with self-catalytic production of nitric oxide for photothermal and gas-combined therapy of tumor, J Colloid Interface Sci, 621 (2022) 77-90.\n[17] C. Liu, X. Yan, Y. Zhang, M. Yang, Y. Ma, Y. Zhang, Q. Xu, K. Tu, M. Zhang, Oral administration of turmeric-derived exosome-like nanovesicles with anti-inflammatory and pro-resolving bioactions for murine colitis therapy, J Nanobiotechnology, 20 (2022) 206.\n[18] Z. Zhong, Y. Xu, J. Liu, C. Zhang, Z. Xiao, Y. Xia, Y. Wang, J. Wang, Q. Xu, Y. Lu, Clinicopathological study of gastric schwannoma and review of related literature, BMC Surg, 22 (2022) 159.\n[19] J. Guo, F. Qiu, J. Zhao, Q. Lu, W. Fu, Q. Xu, D. Huang, Case Report: Retroperitoneal Sarco"

教育背景

  • 2011.09 – 2014.12

    西安交通大学 博士 外科学(肝胆外科)

  • 2004.09 – 2011.07

    西安交通大学 硕士 临床医学

工作经历

暂无内容

荣誉奖项

  1. 肝胰恶性肿瘤精准诊疗创新技术的基础研究及临床推广应用(2022)|浙江省
  2. 肝癌创新诊疗的基础和临床应用研究(2020)|浙江省
  3. 恶性血液病新型诊疗体系和预后模型的建立及应用(2021)|浙江省
  4. 肝胰恶性肿瘤分子标志物与治疗新技术的研究和应用(2016)|浙江省
CD11b agonist GB1275 potentiates oncolytic bacterial therapy against pancreatic cancer in mouse tumor models

CD11b激动剂GB1275增强小鼠肿瘤模型中溶瘤细菌疗法对胰腺癌的治疗效果

2026-08-210
OA
Characterizing gene perturbations in single cells via network divergence analysis

通过网络分歧分析表征单细胞中的基因扰动

2026-04-110
OAAI
Engineered Bacteria Factory Integrating Drug Delivery and Antibody Manufacture for Activating the STING Signal Pathway Mediated Tumor Immunotherapy
2026-02-190
OAAI
UBE2V1 Promotes Hepatocellular Carcinoma Progression by Forming a Positive Feedback Loop with HIF-1α
RESEARCH
IF10.7
2025-12-230
PRE
UBE2K promotes breast cancer growth by ubiquitinating and degrading STUB1 to regulate the PKA/CREB1 signaling pathway, forming a feedback loop

UBE2K通过泛素化并降解STUB1来调节PKA/CREB1信号通路,从而促进乳腺癌的生长,形成了一个反馈环路。

2025-12-210
OAAI
Ubiquitin-specific peptidase 40 promotes cellular proliferation and inhibits apoptosis through deubiquitination-mediated stabilization of c-MYC in acute myeloid leukemia

泛素特异性肽酶40通过去泛素化介导的c-MYC稳定化促进细胞增殖并抑制凋亡,在急性髓系白血病中发挥作用。

2025-12-150
PRE
Hepatic stellate cells shape the ECM-disorganized and immunosuppressive microenvironment via CCL11/CCR3 axis in lenvatinib-treated hepatocellular carcinoma

肝星状细胞通过CCL11/CCR3轴塑造了lenvatinib处理的肝细胞癌中的ECM紊乱和免疫抑制性微环境。

2025-11-260
PRE
Retraction Note: Carbon dot nanozymes as free radicals scavengers for the management of hepatic ischemia-reperfusion injury by regulating the liver inflammatory network and inhibiting apoptosis

撤稿说明:碳点纳米酶作为自由基清除剂,通过调控肝脏炎症网络并抑制凋亡,用于肝缺血再灌注损伤的管理

2025-11-180
OAAI
Dual-Defect Engineering of LDH-Based Nanozymes to Enhance Antioxidative Effects in Ischemia Stroke-Reperfusion Injury

基于LDH的纳米酶的双缺陷工程以增强缺血性卒中再灌注损伤中的抗氧化效果

2025-10-270
PRE
Retraction notice to “LncRNA LINC00689 promotes the growth, metastasis and glycolysis of glioma cells by targeting miR-338–3p/PKM2 axis” [Biomed. Pharmacother. 117 (2019) 109069]

撤稿声明针对“LncRNA LINC00689通过靶向miR-338–3p/PKM2轴促进胶质瘤细胞的生长、转移和糖酵解”[Biomed. Pharmacother. 117 (2019) 109069]

2025-09-170
OAAI
Predicting textbook outcome after pancreaticoduodenectomy for invasive intraductal papillary mucinous neoplasm: An international validation cohort study

预测侵袭性导管内乳头状黏液性肿瘤行胰十二指肠切除术后的教科书式结局:一项国际验证队列研究

Surgery
IF2.7
2025-08-290
PRE
Electric-Field-Mediated In Situ Electrocatalysis for Enhanced Chemodynamic Therapy and Immunotherapy via 3D Electrode Arrays

电场介导的原位电催化用于通过3D电极阵列增强化学动力学疗法和免疫疗法

2025-08-280
PRE
The RNA-binding protein CELF1 targets ATG5 to regulate autophagy and promote drug resistance in acute myeloid leukemia

RNA结合蛋白CELF1靶向ATG5以调控自噬并促进急性髓系白血病中的药物抵抗。

2025-08-080
OA
GTF3C2 Promotes the Proliferation of Hepatocellular Carcinoma Cells through the USP21/MEK2/ERK1/2 Pathway

GTF3C2通过USP21/MEK2/ERK1/2通路促进肝癌细胞增殖

2025-02-110
OAAI
Inhibition of Endoplasmic Reticulum Stress Cooperates with SLC7A11 to Promote Disulfidptosis and Suppress Tumor Growth upon Glucose Limitation

抑制内质网应激与SLC7A11协同促进二硫凋亡并抑制葡萄糖限制下的肿瘤生长

2024-12-304
OAAI
USP24 promotes hepatocellular carcinoma tumorigenesis through deubiquitinating and stabilizing TRAF2
2024-11-011
OAAI
Tumor suppressor BAP1 suppresses disulfidptosis through the regulation of SLC7A11 and NADPH levels

肿瘤抑制因子BAP1通过调节SLC7A11和NADPH水平抑制二硫凋亡

2024-09-120
OAAI
Nanoreactors with Cascade Catalytic Activity Reprogram the Tumor Microenvironment for Enhanced Immunotherapy by Synchronously Regulating Treg and Macrophage Cells

具有级联催化活性的纳米反应器通过同步调节Treg和巨噬细胞来重新编程肿瘤微环境以增强免疫治疗

2024-09-060
PRE
UCHL3 promotes hepatocellular carcinoma progression by stabilizing EEF1A1 through deubiquitination
2024-07-041
OAAI
WTAP/IGF2BP3-mediated GBE1 expression accelerates the proliferation and enhances stemness in pancreatic cancer cells via upregulating c-Myc

WTAP/IGF2BP3-mediated GBE1表达通过上调c-myc促进胰腺癌细胞增殖并增强其干细胞性

2024-07-030
OAAI