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RNA m^(6)A reader YTHDF2 facilitates precursor miR-126 maturation to promote acute myeloid leukemia progression

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Genes & Diseases 2024年第1期11卷 382-396页

作者： Zheng Zhang Keren Zhou Li Han Andrew Small Jianhuang Xue Huilin Huang Hengyou weng Rui Su Brandon Tan Chao Shen wei Li Zhicong Zhao Ying Qing Xi Qin Kitty Wang Keith Leung Mark Boldin Chun-wei Chen David Ann Zhijian Qian Xiaolan Deng Jianjun Chen Zhenhua Chen Department of Systems Biology Beckman Research Institute of City of HopeMonroviaCA 91016USA Irell and Manella Graduate School of Biological Sciences Beckman Research Institute of City of HopeDuarteCA 91010USA Gehr Family Center for Leukemia Research City of HopeDuarteCA 91010USA Sun Yat-sen University Cancer Center State Key Laboratory of Oncology in South ChinaCollaborative Innovation Center for Cancer MedicineGuangzhouGuangdong 510060China Guangzhou Laboratory GuangzhouGuangdong 510005China Bioland Laboratory GuangzhouGuangdong 51005China Department of Liver Surgery Renji HospitalShanghai Jiao Tong University School of MedicineShanghai 200127China Department of Diabetes Complications and Metabolism Beckman Research Institute of City of HopeDuarteCA 91010USA Department of Biochemistry and Molecular Biology University of FloridaGainesvilleFL 32603USA Tongji Hospital Affiliated to Tongji University Frontier Science Center for Stem Cell ResearchSchool of Life Sciences and TechnologyTongji UniversityShanghai 200092China School of Pharmacy China Medical UniversityShenyangLiaoning 110001China

As the most common internal modification of mRNA,Ne-methyladenosine(m^(6)A)and its regulators modulate gene expression and play critical roles in various biological and patholog-ical processes including tumorigenesis.It was reported previously that m^(6)A methyltransferase(writer),methyltransferase-like 3(METTL3)adds m^(6)A in primary microRNAs(pri-miRNAs)and fa-cilitates its processing into precursor miRNAs(pre-miRNAs).However,it is unknown whether m^(6)A modification also plays a role in the maturation process of pre-miRNAs and(if so)whether such a function contributes to tumorigenesis.Here,we found that YTHDF2 is aberrantly overexpressed in acute myeloid leukemia(AML)patients,especially in relapsed patients,and plays an onco-genic role in AML.Moreover,YTHDF2 promotes expression of miR-126-3p(also known as miR-126,as it is the main product of precursor miR-126(pre-miR-126)),a miRNA that was reported as an oncomiRNA in AML,through facilitating the processing of pre-miR-126 into mature miR-126.Mechanistically,YTHDF2 recognizes m^(6)A modification in pre-miR-126 and recruits AGO2,a regulator of pre-miRNA processing,to promote the maturation of pre-miR-126.YTHDF2 posi-tively and negatively correlates with miR-126 and miR-126's downstream target genes,respec-tively,in AML patients,and forced expression of miR-126 could largely rescue YTHDF2/Ythdf2 depletion-mediated suppression on AML cell growth/proliferation and leukemogenesis,indi-cating that miR-126 is a functionally important target of YTHDF2 in AML.Overall,our studies not only reveal a previously unappreciated YTHDF2/miR-126 axis in AML and highlight the ther-apeutic potential of targeting this axis for AML treatment,but also suggest that m^(6)A plays a role in pre-miRNA processing that contributes to tumorigenesis.

关键词： AML miR-126 N^(6)-methyladenosine Pre-miRNA maturation YTHDF2

Stabilized cathode/sulfide solid electrolyte interface via Li_(2)ZrO_(3)coating for all-solid-state batteries

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Rare Metals 2022年第11期41卷 3639-3645页

作者： Chen Zhao Zi-Qiang Liu wei weng Ming Wu Xiao-Yan Yan Jing Yang Huan-Ming Lu Xia-Yin Yao School of Materials Scienceand Engineering Taiyuan Universityof Scienceand TechnologyTaiyuan 030024China Ningbo Institute of Materials Technology and Engineering Chinese Academy of SciencesNingbo315201China Center of Materials Science and Optoelectronics Engineering University of Chinese Academy of SciencesBeijing100049China

High-capacity LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)(NCM)cathode is essential for realizing high energy density all-solid-state lithium batteries.However,the space charge layer effect between NCM cathode and the commonly used sulfide solid electrolyte results in deterioration of the battery performance.In this work,a 10-nm electrochemical stable Li_(2)ZrO_(3)(LZO)layer was in situ coated on the surface of NCM particles through facile wet chemical method.

关键词： battery electrolyte solid

XELOX(capecitabine plus oxaliplatin)plus bevacizumab(anti-VEGF-A antibody)with or without adoptive cell immunotherapy in the treatment of patients with previously untreated metastatic colorectal cancer:a multicenter,open-label,randomized,controlled,phase 3 trial

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Signal Transduction and Targeted Therapy 2024年第5期9卷 2104-2113页

作者： Qiu-Zhong Pan Jing-Jing Zhao Liang Liu Dong-Sheng Zhang Li-Ping Wang Wen-wei Hu De-Sheng weng Xiang Xu Yi-Zhuo Li Yan Tang wei-Hong Zhang Jie-Yao Li Xiao Zheng Qi-Jing Wang Yong-Qiang Li Tong Xiang Li Zhou Shuang-Ning Yang Chen Wu Rong-Xing Huang Jia He wei-Jiao Du Lu-Jun Chen Yue-Na Wu Bin Xu Qiong Shen Yi Zhang Jing-Ting Jiang Xiu-Bao Ren Jian-Chuan Xia State Key Laboratory of Oncology in South China Guangdong Provincial Clinical Research Center for CancerCollaborative Innovation Center for Cancer MedicineSun Yat-Sen University Cancer CenterGuangzhouGuangdong 510060PR China Department of Biotherapy Sun Yat-Sen University Cancer CenterGuangzhouGuangdong 510060PR China Tianjin Medical University Cancer Institute and Hospital National Clinical Research Center for CancerTianjin 300060PR China Key Laboratory of Cancer Immunology and Biotherapy Tianjin 300060PR China Department of Biotherapy/Immunology Tianjin Medical University Cancer Institute and HospitalTianjin 300060PR China Department of Medical Oncology Sun Yat-sen University Cancer CenterGuangzhou 510060PR China Department of Oncology the First Affiliated Hospital of Zhengzhou UniversityZhengzhou 450052PR China Department of Tumor Biological Treatment the Third Affiliated Hospital of Soochow UniversityChangzhouJiangsu 213003PR China Jiangsu Engineering Research Center for Tumor Immunotherapy ChangzhouJiangsu 213003PR China Institute for Cell Therapy of Soochow University ChangzhouJiangsu 213003PR China Department of Stem Cell&Regenerative Medicine State Key Laboratory of TraumaBurn and Combined InjuryDaping HospitalArmy Medical UniversityChongqing 400042PR China Imaging Diagnosis and Interventional Center Sun Yat-sen University Cancer CenterGuangzhouGuangdong 510060PR China

Fluoropyrimidine-based combination chemotherapy plus targeted therapy is the standard initial treatment for unresectable metastatic colorectal cancer(mCRC),but the prognosis remains poor.This phase 3 trial(ClinicalTrials.gov:NCT03950154)assessed the efficacy and adverse events(AEs)of the combination of PD-1 blockade-activated DC-CIK(PD1-T)cells with XELOX plus bevacizumab as a first-line therapy in patients with mCRC.A total of 202 participants were enrolled and randomly assigned in a 1:1 ratio to receive either first-line XELOX plus bevacizumab(the control group,n=102)or the same regimen plus autologous PD1-T cell immunotherapy(the immunotherapy group,n=100)every 21 days for up to 6 cycles,followed by maintenance treatment with capecitabine and bevacizumab.The main endpoint of the trial was progression-free survival(PFS).The median follow-up was 19.5 months.Median PFS was 14.8 months(95%CI,11.6-18.0)for the immunotherapy group compared with 9.9 months(8.0-11.8)for the control group(hazard ratio[HR],0.60[95%CI,0.40-0.88];p=0.009).Median overall survival(OS)was not reached for the immunotherapy group and 25.6 months(95%CI,18.3-32.8)for the control group(HR,0.57[95%CI,0.33-0.98];p=0.043).Grade 3 or higher AEs occurred in 20.0%of patients in the immunotherapy group and 23.5%in the control groups,with no toxicity-associated deaths reported.The addition of PD1-T cells to first-line XELOX plus bevacizumab demonstrates significant clinical improvement of PFS and OS with well tolerability in patients with previously untreated mCRC.

关键词： PD1 immunotherapy bevacizumab

Catalytic decomposition of methane to produce hydrogen:A review

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Journal of Energy Chemistry 2021年第7期30卷 415-430页

作者： Zeyu Fan wei weng Jing Zhou Dong Gu wei Xiao School of Resource and Environmental Sciences Hubei International Scientiﬁc and Technological Cooperation Base of Sustainable Resource and EnergyWuhan UniversityWuhan 430072HubeiChina College of Chemistry and Molecular Sciences Hubei Key Laboratory of Electrochemical Power SourcesWuhan UniversityWuhan 430072HubeiChina The Institute for Advanced Studies Wuhan UniversityWuhan 430072HubeiChina

The increasing demands of hydrogen and the recent discovery of large reserves of methane have prompted the conversion of methane to hydrogen.The challenges raised by intensive CO_(2) emission from the traditional conversion of methane have provoked emission-free hydrogen production from methane.The catalytic decomposition of methane(CDM) to produce hydrogen and advanced carbon hence comes into consideration due to the short process and environmental benignity.Although many researchers have made considerable progress in CDM research on the laboratory scale,CDM is still in its infancy in industrialization.The history of its development,fundamental mechanisms,and recent research progress in catalysts and catalytic systems are herein highlighted.The problems of catalytic interface degradation are reviewed,focusing on deactivation from coke deposition in the CDM process.The introduction of a liquid phase interface which can in-situ remove carbon products provides a new strategy for this process.Furthermore,the challenges and prospects for future research into novel CDM catalysts or catalyst systems are included.

关键词： Hydrogen production Methane decomposition Metal-based catalysts Carbon-based catalysts Liquid catalyst

Interfacial confinement of Ni-V2O3 in molten salts for enhanced electrocatalytic hydrogen evolution

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Journal of Energy Chemistry 2020年第11期29卷 280-285页

作者： Jing Zhou Hansheng Xiao wei weng Dong Gu wei Xiao College of Chemistry and Molecular Sciences Hubei Key Laboratory of Electrochemical Power SourcesWuhan UniversityWuhan 430072HubeiChina School of Resource and Environmental Sciences Hubei International Scientific and Technological Cooperation Base of Sustainable Resource and EnergyWuhan UniversityWuhan 430072HubeiChina The Institute of Advanced Studies.Wuhan University Wuhan 430072HubeiChina

Implementation of non-precious electrocatalysts is key-enabling for water electrolysis to relieve challenges in energy and environmental sustainability. Self-supporting Ni-V2O3 electrodes consisting of nanostrip-like V2O3 perpendicularly anchored on Ni meshes are herein constructed via the electrochemical reduction of soluble NaVO3 in molten salts for enhanced electrocatalytic hydrogen evolution. Such a special configuration in morphology and composition creates a well confined interface between Ni and V2O3. Experimental and Density-Functional-Theory results confirm that the synergy between Ni and V2O3 accelerates the dissociation of H2O for forming hydrogen intermediates and enhances the combination of H*for generating H2.

关键词： Hydrogen evolution Electrochemistry Molten salt Ni V2O3

Effects of K and Mn promoters over Fe2O3 on Fischer–Tropsch synthesis

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Journal of Energy Chemistry 2020年第8期29卷 118-127,I0004页

作者： Teng Lv wei weng Jing Zhou Dong Gu wei Xiao School of Resource and Environmental Sciences Hubei International Scientific and Technological Cooperation Base of Sustainable Resource and EnergyWuhan UniversityWuhan 430072HubeiChina The Institute for Advanced Studies Wuhan UniversityWuhan 430072.HubeiChina

Structural and compositional design of core-shell structure is an effective strategy towards enhanced catalysis.Herein,amorphous MnO2 nanosheets and K+-intercalated layered MnO2 nanosheets are controllably assembled over Fe2O3 spindles,in which the MnO2 nanosheets are perpendicularly anchored to the surface of Fe2O3.Such a core shell structure contributes to a high specific surface area and abundant pore channels on the surface of catalysts.In addition,the existence of K+provides large numbers of basic sites and restrains the formation of unpleasant(Fe1-xMnx)3O4.Benefiting from the merits in structure and composition,CO adsorption is enhanced and remaining time of intermediates is prolonged on the surfaces of catalysts during the Fischer–Tropsch synthesis(FTS),facilitating to the formation of active iron carbides and C–C coupling reactions.Resultantly,the Fe2O3@K+-Mn O2 shows both a high CO conversion of 82.3%and a high C5+ selectivity of 73.1%.The present study provides structural and compositional rationales on design high-performance catalysts towards FTS.

关键词： Fischer–Tropsch synthesis K promoter Mn promoter CO conversion C5+selectivity

Controllable conversion of rice husks to Si/C and SiC/C composites in molten salts

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Journal of Energy Chemistry 2021年第4期30卷 102-107页

作者： Da Pang wei weng Jing Zhou Dong Gu wei Xiao School of Resource and Environmental Sciences Hubei International Scientific and Technological Cooperation Base of Sustainable Resource and EnergyWuhan UniversityWuhan 430072HubeiChina College of Chemistry and Molecular Sciences Hubei Key Laboratory of Electrochemical Power SourcesWuhan UniversityWuhan 430072HubeiChina The Institute of Advanced Studies Wuhan UniversityWuhan 430072HubeiChina

Direct conversion of biomass to functional materials is an ideal solution to relieve challenges in environmental and energy sustainability.We herein demonstrate a molten salt thermoelectrolysis of rice husks(RHs)mainly consisting of organic mass and biosilica to achieve high-efficiency and upgraded utilization of both Si and C in RHs.By coupling pyrolysis of organic mass with electrochemical reduction of silica in molten salts,the thermoelectrolysis of RHs in molten CaCl_(2)-NaCl at 800℃ refines the RHs and acidleached RHs to SiC nanowire/C(SiC-NW/C)and Si nanoparticle/C(Si-NP/C),respectively.The present study highlights the molten salt thermoelectrolysis for reclamation of biomass wastes in an affordable and controllable manner.

关键词： Rice husks Molten salt Silicon Silicon carbide Electrochemistry

Enhanced electrodeposition and separation of metallic Cr from soluble K2CrO4 on a liquid Zn cathode

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Journal of Energy Chemistry 2020年第1期29卷 204-211,I0007页

作者： wei weng Zhi Wang Zhancheng Guo Shuqiang Jiao Mingyong Wang State Key Laboratory of Advanced Metallurgy University of Science and Technology BeijingBeijing 100083China School of Resource and Environmental Sciences Hubei International Scientific and Technological Cooperation Base of Sustainable Resource and EnergyWuhan UniversityWuhan 430072HubeiChina Key Laboratory of Green Process and Engineering National Engineering Laboratory for Hydrometallurgical Cleaner Production TechnologyInstitute of Process EngineeringChinese Academy of SciencesBeijing 100190China

Carbon contamination and the formation of low-valence oxides limit the preparation of refractory metals by molten salt electrolysis.In this paper,a liquid Zn cathode is adopted for the electrochemical reduction of soluble K2CrO4 to metallic Cr in CaCl2-KCl molten salt.It is found that CrO4^2-can be directly electrochemically reduced to Cr via a six-electron-transfer step and low-valence Cr oxides is hardly produced.The reduction rate is obviously increased from 16.7 mgCrh^-1cm^-2 on the solid Mo cathode to58.7 mgCrh-1cm-2on liquid Zn cathode.The electrodeposited Cr is distributed in liquid Zn cathode.Carbon contamination is effectively avoided due to the negligible solubility of carbon in the liquid Zn cathode.Furthermore,Cr can be effectively separated and enriched to the bottom of liquid Zn under supergravity field,realizing the efficient acquisition of metallic Cr and recycling of liquid Zn.The method herein provides a promising route for the preparation of refractory metals with high-purity by molten salt electrolysis.

关键词： Molten salt electrolysis Liquid Zn cathode Carbon contamination K2CrO4 Metallic Cr

高效液相色谱-质谱技术在蛋白质组学中的应用

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色谱 2024年第7期42卷 601-612页

作者：刘威翁凌霄高明霞张祥民复旦大学化学系上海200438 复旦大学生物医学研究院上海200032

蛋白质组学研究在生物医学领域发挥了重要作用,然而研究面临的主要难点在于其研究对象的复杂性和多样性。随着质谱技术的快速发展,高效液相色谱-质谱(HPLC-MS)分离分析复杂生物样品已经成为蛋白质组学研究的基础工具。蛋白质组学的研究... 详细信息

蛋白质组学研究在生物医学领域发挥了重要作用,然而研究面临的主要难点在于其研究对象的复杂性和多样性。随着质谱技术的快速发展,高效液相色谱-质谱(HPLC-MS)分离分析复杂生物样品已经成为蛋白质组学研究的基础工具。蛋白质组学的研究从肽段分离,延伸到蛋白质和蛋白质复合物的分离,随着分析物的分子质量不断增大,其结构和组成复杂性也持续增加,分子特性也发生改变。面对不同的蛋白质组学研究对象,选择不同的分离模式、分离条件以及固定相参数是进行深度蛋白质组学研究的关键。本文综述了实验室常用的液相色谱分离模式,包括反相色谱(RPLC)、亲水相互作用色谱(HILIC)、疏水相互作用色谱(HIC)、离子交换色谱(IEC)和体积排阻色谱(SEC),以及其不同的组合模式与质谱联用在自下而上(bottom-up)分析、自上而下(top-down)分析、蛋白-蛋白相互作用分析中应用的研究。具体分析了色谱流动相与被分析对象之间的兼容性问题、色谱流动相与质谱兼容性问题,以及多维色谱中不同色谱模式之间流动相的兼容性问题。重点关注存在不兼容问题时研究者所提出的解决方案。此外,本文还评述了HPLC-MS结合样本前处理的方法在外泌体和单细胞蛋白质组学中的应用研究。总之,文章聚焦于近年来HPLC-MS技术在蛋白质组学中的研究进展,旨在为未来蛋白质组学领域的研究提供参考。

关键词：高效液相色谱反相液相色谱亲水相互作用色谱疏水作用色谱离子交换色谱体积排阻色谱蛋白质组学