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Long noncoding RNA LINC01106 promotes lung adenocarcinoma progression via upregulation of autophagy

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Oncology Research 2025年第1期33卷 171-184页

作者： GENGYUN SUN YIPING ZHENG JIANFENG CAI JIE GAO LIE DONG XIANGBIN ZHANG YINGHUI HUANG department of respiratory and Critical Care Medicine The First Affiliated Hospital of Anhui Medical UniversityHefei230022China department of respiratory and Critical Care Medicine Nanping First Hospital Affiliated to Fujian Medical UniversityNanping353006China

Background:Long noncoding RNA,LINC01106 exhibits high expression in lung adenocarcinoma(LUAD)tumor tissues,but its functional role and regulatory mechanism in LUAD cells remain ***:LINC01106 expression was analyzed in LUAD tissues and its functional impact on LUAD cells was *** cells were silenced with sh-LINC01106 and injected into nude mice to investigate tumor *** downstream transcription factors and molecular mechanism were determined using the Human transcription factor database(TFDB)database and Gene Expression Profiling Interactive Analysis(GEPIA)***,the impact of linc01106 on autophagy was analyzed by determining the expression of autophagy-related genes(ATGs)in LUAD ***:Our results showed that LINC01106 exhibited upregulation in both LUAD tissues and cell *** silencing of LINC01106 demonstrated a suppressive effect on tumorigenesis in a xenograft mouse model of ***,LINC01106 was found to recruit TATA-binding protein-associated factor 15(TAF15),an RNA-binding protein,thereby enhancing the mRNA stability of TEA domain transcription factor 4(TEAD4).In turn,TEAD4 served as a transcription factor that bound to the LINC01106 promoter and regulated its *** assays indicated that LINC01106 promoted autophagy in LUAD cells by upregulating the expression of autophagy-related genes(ATGs).The silencing of LINC01106 in LUAD cells inhibited autophagy,and cell proliferation,and promoted apoptosis,which all were effectively reversed by ATG5 ***:Overall,LINC01106,transcriptionally activated by TEAD4,interacts with TAF15 to promote the stability of TEAD4 and upregulates the expression of ATGs,promoting malignancy of LUAD cells.

关键词： LINC01106 TAF15 TEAD4 ATG5 Lung adenocarcinoma(LUAD) Non-small cell lung cancer(NSCLC)

Incidence of hematological toxicity with use of immunotherapy and chemotherapy in advanced non-small cell lung cancer

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中华医学杂志(英文版) 2025年第2期138卷 2024 Sep 19页

作者： Fu Wenhai Jiang Yu Ye Wenjun Zhong Ran Xiong Shan Li Jianfu Li Caichen He Jianxing Liang Wenhua department of Thoracic Surgery and Oncology The First Affiliated Hospital of Guangzhou Medical University Guangzhou Guangdong China State Key Laboratory of respiratory Disease Guangzhou Guangdong China National Clinical Research Center for respiratory Disease Guangzhou Guangdong China Guangzhou Institute of respiratory Health Guangzhou Guangdong China

Knotting ligands to control metal coordination geometry

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Science China Chemistry 2025年第2期68卷 403-404页

作者： Fabien B.L.Cougnon department of Chemistry and Nanoscience centre University of JyväskyläJyväskyläFinland

Zinc is a metal of particular importance for life[1].It is the most abundant transition metal in biological systems after iron and contributes both structural and catalytic roles to many cellular *** properties of Zn^(Ⅱ),unlike those of any other first-row transition metal ions,explain its biological *** to its filled d-shell orbitals,Zn^(Ⅱ) is redox-stable,has a ligand-field energy stabilization of zero and,consequently,no typical coordination number and *** metalloproteins exploit these features to carry a broad range of chemical reactions in mild *** metalloenzymes,unsaturated ZnII centres often act as redox-stable Lewis *** protein backbone provides a highly preorganized environment around the metal centre and accompanies the changes in coordination geometry occurring as substrate transformation proceeds,thereby modulating the metal reactivity.

关键词： coordination geometry centre

A Greener Future: Carbon Nanomaterials from Lignocellulose

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Journal of Renewable Materials 2025年第1期13卷 21-47页

作者： Hebat-Allah S.Tohamy Mohamed El-Sakhawy Samir Kamel Cellulose and Paper department National Research CentreDokkiGiza12622Egypt

Lignocellulosic materials(LCMs),abundant biomass residues,pose signiﬁcant environmental challenges when improperly disposed ***,such as sugarcane bagasse,rice straw,saw dust and agricultural residues,are abun-dant but often burned,contributing to air pollution and greenhouse gas *** review explores the potential of transforming these materials into high-value carbon nanomaterials(CNMs).We explore the potential of transforming these materials into high-value *** employing techniques like carbonization and activa-tion,LCMs can be converted into various CNMs,including carbon nanotubes(CNTs),graphene(G),graphene oxide(GO),carbon quantum dots(CQDs),nanodiamonds(NDs),fullerenes(F),carbon nanoﬁbers(CNFs),and *** different carbon allotropes further enhances their *** derived from cellulose,lignin,and hemicellulose exhibit promising applications in diverseﬁ*** instance,CNTs can be used in energy storage devices like batteries and supercapacitors due to their exceptional electrical conductivity and mechanical ***,CNTs can be incorporated into recycled paper as aﬁre retardant additive,enhancing itsﬂame resistance.G,renowned for its high surface area and excellent electrical conductivity,ﬁnds applications in electronics,sensors,catalysis,and water treatment,where it can be used to adsorb heavy metal ***,owing to their unique optical properties,are used in bioimaging,drug delivery,and optoelectronic *** harnessing the potential of LCMs,we can not only mitigate environmental concerns but also contri-bute to a sustainable *** research is essential to optimize synthesis methods,explore novel applica-tions,and unlock the full potential of these versatile materials.

关键词： Lignocellulosic materials carbon-based nanomaterials carbon allotropes

Acellular scaffold‑based approach for in situ genetic engineering of host T‑cells in solid tumor immunotherapy

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Military Medical Research 2025年第1期12卷 16-35页

作者： Hiren Y.Dandia Mamatha M.Pillai Deepak Sharma Meghna Suvarna Neha Dalal Ayush Madhok Arvind Ingle Shubhada V.Chiplunkar Sanjeev Galande Prakriti Tayalia department of Biosciences and Bioengineering Indian Institute of Technology BombayPowaiMumbai 400076India Radiation Biology and Health Sciences Division Bhabha Atomic Research CentreMumbai 400085India centre of Excellence in Epigenetics Department of BiologyIndian Institute of Science Education and ResearchPune 411008India Advanced centre for Treatment Research and Education in Cancer(ACTREC)Tata Memorial CentreKhargharMumbai 410210India

Background:Targeted T-cell therapy has emerged as a promising strategy for the treatment of hematological ***,its application to solid tumors presents significant challenges due to the limited accessibility and *** delivery of tumor-specific T-cells using biomaterials has shown promise,however,procedures required for genetic modification and generation of a sufficient number of tumor-specific T-cells ex vivo remain major obstacles due to cost and time ***:Polyethylene glycol(PEG)-based three-dimensional(3D)scaffolds were developed and conjugated with positively charged poly-L-lysine(PLL)using carbamide chemistry for efficient loading of lentiviruses(LVs)carrying tumor antigen-specific T-cell receptors(TCRs).The physical and biological properties of the scaffold were extensively ***,the scaffold loaded with OVA-TCR LVs was implanted in B16F10 cells expressing ovalbumin(B16-OVA)tumor model to evaluate the anti-tumor response and the presence of transduced ***:Our findings demonstrate that the scaffolds do not induce any systemic inflammation upon subcutaneous implantation and effectively recruit T-cells to the *** B16-OVA melanoma tumor-bearing mice,the scaffolds efficiently transduce host T-cells with OVA-specific *** genetically modified T-cells exhibit homing capability towards the tumor and secondary lymphoid organs,resulting in a significant reduction of tumor size and systemic increase in anti-tumor *** cell profiling revealed a significantly high percentage of transduced T-cells and a notable reduction in suppressor immune cells within the tumors of mice implanted with these ***:Our scaffold-based T-cell therapy presents an innovative in situ localized approach for programming T-cells to target solid *** approach offers a viable alternative to in vitro manipulation of T-cells,circumventing the need for large-scale in vitro generat

关键词： Polyethylene glycol diacrylate Poly-L-lysine Lentiviruses T-cell therapy B16F10-OVA melanoma

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CAF-derived exosome-miR-3124-5p promotes malignant biological processes in NSCLC via the TOLLIP/TLR4-MyD88-NF-κB pathway

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Oncology Research 2025年第1期33卷 133-148页

作者： TAO SUN QINGHUA SONG HUA LIU department of respiratory and Critical Care Medicine Affiliated Hospital of Nantong UniversityMedical School of Nantong UniversityNantong226001China department of Emergency The People’s Hospital of RugaoNantong226500China department of Haematology The People’s Hospital of RugaoNantong226500China

Background:Lung cancer is a life-threatening disease that occurs worldwide,but is especially common in *** crucial role of the tumour microenvironment(TME)in non-small cell lung cancer(NSCLC)has attracted recent ***-associated fibroblasts(CAFs)are the main factors that contribute to the TME function,and CAF exosomes are closely linked to ***:The expression levels of miR-3124-5p and Toll-interacting protein(TOLLIP)were analysed by bioinformatics prediction combined with RT-qPCR/Western Blot *** were isolated and identified from clinical NSCLC *** electron microscopy and Western Blot were used to identify exosomes from these *** in proliferation(CCK-8 and clone formation),migration(wound healing),and invasion(transwell)of NSCLC cells were *** Luciferase reporter test was applied to clarify the binding of miR-3124-5p to *** TOLLIP/TLR4/MyD88/NF-κB pathway proteins were determined using Western blot ***:MiR-3124-5p is overexpressed in clinical tissues and cells of ***-3124-5p was dramatically enriched in CAF-derived *** experiments revealed that CAFs delivered miR-3124-5p into NSCLC cells via exosomes,stimulating cancer cell ***-3124-5p acted as a sponge to negatively regulate TOLLIP expression,which activated the TLR4/MyD88/NF-κB axis to promote the occurrence and development of *** salvage tests were performed to determine whether CAF-exosome-derived miR-3124-5p plays a pro-cancer role in NSCLC by affecting the TOLLIP signalling ***:These results provide an interesting direction for the diagnosis and therapy of NSCLC.

关键词： Non-small cell lung cancer(NSCLC) Cancer-associated fibroblasts(CAFs) Exosomes miR-3124-5p Toll-interacting protein(TOLLIP)

Stepping up after spinal cord injury:negotiating an obstacle during walking

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Neural Regeneration Research 2025年第7期20卷 1919-1929页

作者： Alain Frigon Charly G.Lecomte department of Pharmacology-Physiology Faculty of Medicine and Health SciencesUniversitéde SherbrookeCentre de recherche du Centre Hospitalier Universitaire de SherbrookeSherbrookeQCCanada

Every day walking consists of frequent voluntary modifications in the gait pattern to negotiate *** spinal cord injury,stepping over an obstacle becomes *** over an obstacle requires sensorimotor transformations in several structures of the brain,including the parietal cortex,premotor cortex,and motor *** information and planning are transformed into motor commands,which are sent from the motor cortex to spinal neuronal circuits to alter limb trajectory,coordinate the limbs,and maintain *** spinal cord injury,bidirectional communication between the brain and spinal cord is disrupted and animals,including humans,fail to voluntarily modify limb trajectory to step over an ***,in this review,we discuss the neuromechanical control of stepping over an obstacle,why it fails after spinal cord injury,and how it recovers to a certain extent.

关键词： biomechanics locomotion neurophysiology obstacle negotiation spinal cord injury

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Personalized federated few-shot node classification

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Science China(Information Sciences) 2025年第1期68卷 204-218页

作者： Yunfeng ZHAO Xintong HE Guoxian YU Jun WANG Yongqing ZHENG Carlotta DOMENICONI School of Software Shandong University Joint SDU-NTU centre for Artificial Intelligence Research Shandong University department of Mathematics National University of Singapore department of Computer Science George Mason University

Personalized federated learning(PFL) aims to train customized models for individual clients in a decentralized setting, with the account of non-independent and identically distributed data across clients. However, most PFL methods adopt uniform classification layers for diverse clients and give rise to error-prone predictions, due to the task heterogeneity notably prominent in decentralized graph data scenarios. Although some PFL solutions setup client-specific classification layers for each client and optimize them only locally, they are corrupted with limited local training data. We propose an innovative solution called federated parameter decoupling and node augmentation(Fed PANo) to address these problems and to achieve personalized federated few-shot node classification, which is a prevalent and challenging but unexplored topic. Specifically, Fed PANo first separates the local model into the GNN and classifier to handle unique client-specific task variations. The GNN is trained through federated learning to capture shared knowledge of graph nodes across clients, while the classifier is custom-designed and trained individually for each client. Additionally, a generic classifier shared among clients is adopted to encourage the GNN's grasp of shared information. Then Fed PANo further proposes the node generator along with its local and collaborative training strategies to deal with the node scarcity of clients. Extensive experimental results on benchmark datasets confirm that Fed PANo outperforms eight competitive baselines across different settings.

关键词： personalized federated learning few-shot learning node classification task heterogeneity parameter decoupling node augmentation

Disentangling the contributing components of stream water by using environmental tracers

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Journal of Mountain Science 2025年第1期22卷 260-277页

作者： Abul Amir KHAN Naresh Chandra PANT Amity centre for Air Pollution Control(ACAPC)&Amity centre for Ocean Atmospheric Science and Technology(ACOAST) Amity University Haryana(AUH)Gurugram-122413India department of Geology University of DelhiNorth CampusDelhi-11007India

Identifying the various components contributing to river discharge can be *** study relies on stable isotopes and electrical conductivity(EC)of water as tracers to distinguish the different components contributing to total river ***,we have made an effort to comprehend the processes that may influence glacier ice melt as well as the limits of oxygen-based hydrograph *** distinct geographic domains in terms of climates and topographies were *** first study site represents the upper Ganga catchment(central Himalaya),while the second site is located in the Chandra sub-basin in western *** in estimating the proportion of glacier melt in isotope mixing model are likely if end-member isotopic compositions,are not well defined,particularly for *** separation results indicate that snowmelt is the largest contributor to total river flow in both *** contribution of snowmelt to the total runoff of the upper Ganga ranged from~60%to 70%.The estimated contributions of glacier melt varied from 36%to 63%in upper Ganga headwater to 6%to 15%at Devprayag and~8%at *** the Hamtah River,glacier and snowmelt contributions,quantified using a two-component mixing model,ranged from 10%to 14%during the pre-and postmonsoon seasons of *** significant spatial and temporal variability,coupled with overlapping isotopic signatures,suggests complex glacio-fluvial interactions in these *** slow-moving air masses with whirling motion closer to the study area irrespective of the direction,and air parcels coming through Bay of Bengal branch are characterized by depleted isotopic rainfall compared to air masses originating from the Arabian Sea.

关键词： Snowmelt Glacier melt Oxygen isotopes Bhagirathi River Alaknanda River Hamtah

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