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Nature Aging 2025年 1-18页

作者： Heo, Gyujin Xu, Ying Wang, Erming Ali, Muhammad Oh, Hamilton Se-Hwee Moran-Losada, Patricia Anastasi, Federica González Escalante, Armand Puerta, Raquel Song, Soomin Timsina, Jigyasha Liu, Menghan Western, Daniel Gong, Katherine Chen, Yike Kohlfeld, Pat Flynn, Allison Thomas, Alvin G. Lowery, Joseph Morris, John C. Holtzman, David M. Perlmutter, Joel S. Schindler, Suzanne E. Vilor-Tejedor, Natalia Suárez-Calvet, Marc García-González, Pablo Marquié, Marta Fernández, Maria Victoria Boada, Mercè Cano, Amanda Ruiz, Agustín Zhang, Bin Bennett, David A. Benzinger, Tammie Wyss-Coray, Tony Ibanez, Laura Sung, Yun Ju Cruchaga, Carlos Department of Psychiatry Washington University School of Medicine St. Louis MO United States NeuroGenomics and Informatics Center Washington University St. Louis MO United States Department of Genetics and Genomic Sciences Icahn School of Medicine at Mount Sinai New York NY United States Mount Sinai Center for Transformative Disease Modeling Icahn School of Medicine at Mount Sinai New York NY United States Graduate Program in Stem Cell and Regenerative Medicine Stanford University Stanford CA United States The Phil and Penny Knight Initiative for Brain Resilience Stanford University Stanford CA United States Wu Tsai Neurosciences Institute Stanford University Stanford CA United States Department of Neurology and Neurological Sciences Stanford University School of Medicine Stanford CA United States Barcelonaβeta Brain Research Center (BBRC) Pasqual Maragall Foundation Barcelona Spain Hospital del Mar Research Institute Barcelona Spain Centre for Genomic Regulation (CRG) Barcelona Institute of Science and Technology (BIST) Barcelona Spain Department of Medicine and Life Sciences Universitat Pompeu Fabra Barcelona Spain Ace Alzheimer Center Barcelona Universitat Internacional de Catalunya Barcelona Spain PhD Program in Biotechnology Faculty of Pharmacy and Food Sciences University of Barcelona Barcelona Spain Department of Neurology Washington University School of Medicine St. Louis MO United States Hope Center for Neurologic Diseases Washington University St. Louis MO United States Knight Alzheimer’s Disease Research Center Washington University St. Louis MO United States Department of Radiology Washington University School of Medicine St. Louis MO United States Department of Genetics Radboud UMC Nijmegen Netherlands Servei de Neurologia Hospital del Mar Barcelona Spain Biomedical Research Networking Centre in Neurodegenerative Diseases (CIBERNED) National Institute of Health Carlos III Madrid Spain Glenn Biggs Institute for Alzheimer’s & Ne

Proteomic studies have been instrumental in identifying brain, cerebrospinal fluid and plasma proteins associated with Alzheimer’s disease (AD). Here, we comprehensively examined 6,905 aptamers corresponding to 6,106 unique proteins in plasma in more than 3,300 well-characterized individuals to identify new proteins, pathways and predictive models for AD. We identified 416 proteins (294 new) associated with clinical AD status and validated the findings in two external datasets representing more than 7,000 samples. AD-related proteins reflected blood–brain barrier disruption and other processes implicated in AD, such as lipid dysregulation or immune responses. A machine learning model was used to identify a set of seven proteins that were highly predictive of both clinical AD (area under the curve (AUC) of >0.72) and biomarker-defined AD status (AUC of >0.88), which were replicated in multiple external cohorts and orthogonal platforms. These findings underscore the potential of using plasma proteins as biomarkers for the early detection and monitoring of AD and for guiding treatment decisions. © The Author(s), under exclusive licence to Springer Nature America, Inc. 2025.

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The Role of Animal-Assisted Therapy in Enhancing Patients' Well-Being: Systematic Study of the Qualitative and Quantitative Evidence

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JMIRx med 2024年 5卷 e51787页

作者： Ramendra Pati Pandey Riya Mukherjee Chung-Ming Chang School of Health Sciences & Technology University of Petroleum and Energy Studies Dehradun Uttarakhand India. Graduate Institute of Biomedical Sciences Chang Gung University Taoyuan Taiwan. Master & PhD Program in Biotechnology Industry Chang Gung University Taoyuan Taiwan. Department of Medical Biotechnology and Laboratory Science Chang Gung University Taoyuan Taiwan.

Background:Animal-assisted therapy, also known as pet therapy, is a therapeutic intervention that involves animals to enhance the well-being of individuals across various populations and settings. Objective:This systematic study aims to assess the outcomes of animal-assisted therapy interventions and explore the associated policies. Methods:A total of 16 papers published between 2015 and 2023 were selected for analysis. These papers were chosen based on their relevance to the research topic of animal-assisted therapy and their availability in scholarly databases. Thematic synthesis and meta-analysis were used to synthesize the qualitative and quantitative data extracted from the selected papers. Results:The analysis included 16 studies that met the inclusion criteria and were deemed to be of moderate or higher quality. Among these studies, 4 demonstrated positive results for therapeutic mediation and one for supportive mediation in psychiatric disorders. Additionally, all studies showed positive outcomes for depression and neurological disorders. Regarding stress and anxiety, 3 studies indicated supportive mediation, while 2 studies showed activating mediation. Conclusions:The overall assessment of animal-assisted therapy shows promise as an effective intervention in promoting well-being among diverse populations. Further research and the establishment of standardized outcome assessment measures and comprehensive policies are essential for advancing the field and maximizing the benefits of animal-assisted therapy.

关键词： animal-assisted therapy outcome assessment pet therapy policies systematic study

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Research highlights

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Lab on a Chip 2013年第10期13卷 1842-1845页

作者： João Ribas Mark W. Tibbitt Mehmet R. Dokmeci Ali Khademhosseini Center for Biomedical Engineering Department of Medicine Brigham and Women's Hospital Harvard Medical School Cambridge Massachusetts 02139 USA Harvard-MIT Division of Health Sciences and Technology Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA PhD Program in Experimental Biology and Biomedicine CNC-Center for Neuroscience and Cell Biology and Institute for Interdisciplinary Research (IIIUC) University of Coimbra 3004-517 Coimbra Portugal Biocant–Center of Innovation and Biotechnology 3060-197 Cantanhede Portugal Department of Chemical and Biological Engineering University of Colorado Boulder Colorado 80303 USA Wyss Institute for Biologically Inspired Engineering Harvard University Boston Massachusetts 02115 USA World Premier International–Advanced Institute for Materials Research (WPI-AIMR) Tohoku University Sendai 980-8577 Japan

A graphical abstract is available for this content

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Research highlights

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Lab on a Chip 2013年第4期13卷 599-601页

作者： Francesco Piraino João Ribas Mehmet R. Dokmeci Ali Khademhosseini Bioengineering Department Politecnico di Milano Piazza Leonardo da Vinci 32 20133 Milano Italy Center for Biomedical Engineering Department of Medicine Brigham and Women's Hospital Harvard Medical School Cambridge Massachusetts 02139 USA Harvard-MIT Division of Health Sciences and Technology Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA Biocant-Center of Innovation and Biotechnology 3060-197 Cantanhede Portugal PhD Program in Experimental Biology and Biomedicine CNC-Centre for Neuroscience and Cell Biology 3004-517 Coimbra Portugal Wyss Institute for Biologically Inspired Engineering Harvard University Boston Massachusetts 02115 USA World Premier International – Advanced Institute for Materials Research (WPI-AIMR) Tohoku University Sendai 980-8577 Japan

A graphical abstract is available for this content

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Correction to: Disturbed Gastrointestinal Contractility in a Polycystic Ovary Syndrome Rat Model

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Digestive diseases and sciences 2020年第11期65卷 3408-3409页

作者： Kai-Lee Wang Shih-Min Hsia Paulus S Wang Po-Han Lin Department of Nursing Ching Kuo Institute of Management and Health No. 336 Fuxsin Rd. Zhongshan Dist. Keelung City 20301 Taiwan Republic of China. d49505002@gm.ym.edu.tw. Department of Physiology School of Medicine National Yang-Ming University Taipei Taiwan Republic of China. d49505002@gm.ym.edu.tw. School of Nutrition and Health Sciences Taipei Medical University Taipei 11031 Taiwan Republic of China. Department of Physiology School of Medicine National Yang-Ming University Taipei Taiwan Republic of China. Department of Medical Research and Education Taipei Veterans General Hospital Taipei Taiwan Republic of China. PhD Program of Aging College of Medicine China Medical University Taichung Taiwan Republic of China. Department of Biotechnology Asia University Taichung Taiwan Republic of China.

The original version of the article unfortunately contained an error in the legend of Figure 5B. Corrected version of Figure 5 is given below.

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Exploring the potential of the nano-based sunscreens and antioxidants for preventing and treating skin photoaging

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Chemosphere 2024年 347卷 140702页

作者： Lin, Chih-Hung Lin, Ming-Hsien Chung, Yu-Kuo Alalaiwe, Ahmed Hung, Chi-Feng Fang, Jia-You Center for General Education Chang Gung University of Science and Technology Kweishan Taoyuan Taiwan Department of Dermatology Chi Mei Medical Center Tainan Taiwan Graduate Institute of Biomedical Sciences Chang Gung University Kweishan Taoyuan Taiwan Department of Pharmaceutics College of Pharmacy Prince Sattam Bin Abdulaziz University Al Kharj Saudi Arabia School of Medicine Fu Jen Catholic University New Taipei City Taiwan PhD Program in Pharmaceutical Biotechnology Fu Jen Catholic University New Taipei City Taiwan School of Pharmacy Kaohsiung Medical University Kaohsiung Taiwan Pharmaceutics Laboratory Graduate Institute of Natural Products Chang Gung University Kweishan Taoyuan Taiwan Research Center for Food and Cosmetic Safety and Research Center for Chinese Herbal Medicine Chang Gung University of Science and Technology Kweishan Taoyuan Taiwan Department of Anesthesiology Chang Gung Memorial Hospital Kweishan Taoyuan Taiwan

Excessive exposure to sunlight, especially UV irradiation, causes skin photodamage. Sunscreens, such as TiO2 and ZnO, can potentially prevent UV via scattering, reflection, and absorption. Topical antioxidants are another means of skin photoprotection. Developing nanoparticles for sunscreens and antioxidants is recommended for photoaging prevention and treatment as it can improve uncomfortable skin appearance, stability, penetration, and safety. This study reviewed the effects of nano-sized sunscreens and antioxidants on skin photoprevention by examining published studies and articles from PubMed, Scopus, and Google Scholar, which explore the topics of skin photoaging, skin senescence, UV radiation, keratinocyte, dermal fibroblast, sunscreen, antioxidant, and nanoparticle. The researchers of this study also summarized the nano-based UV filters and therapeutics for mitigating skin photoaging. The skin photodamage mechanisms are presented, followed by the introduction of current skin photoaging treatment. The different nanoparticle types used for topical delivery were also explored in this study. This is followed by the mechanisms of how nanoparticles improve the UV filters and antioxidant performance. Lastly, recent investigations were reviewed on nanoparticulate sunscreens and antioxidants in skin photoaging management. Sunscreens and antioxidants for topical application have different concepts. Topical antioxidants are ideal for permeating into the skin to exhibit free radical scavenging activity, while UV filters are prescribed to remain on the skin surface without absorption to exert the UV-blocking effect without causing toxicity. The nanoparticle design strategy for meeting the different needs of sunscreens and antioxidants is also explored in this study. Although the benefits of using nanoparticles for alleviating photodamage are well-established, more animal-based and clinical studies are necessary. © 2023 Elsevier Ltd

关键词： Antioxidants

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The genome-wide association study of serum IgE levels demonstrated a shared genetic background in allergic diseases

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Clinical immunology (Orlando, Fla.) 2024年 260卷 109897页

作者： Hsing-Fang Lu Chen-Hsing Chou Ying-Ju Lin Shunsuke Uchiyama Chikashi Terao Yu-Wen Wang Jai-Sing Yang Ting-Yuan Liu Henry Sung-Ching Wong Sean Chun-Chang Chen Fuu-Jen Tsai Department of Medical Research China Medical University Hospital Taichung 404327 Taiwan Laboratory for Statistical and Translational Genetics RIKEN Center for Integrative Medical Sciences Yokohama Japan. PhD Program for Health Science and Industry College of Health Care China Medical University Taichung Taiwan Department of Health Services Administration China Medical University Taichung Taiwan. Genetic Center Department of Medical Research China Medical University Hospital Taichung Taiwan School of Chinese Medicine China Medical University Taichung Taiwan. Laboratory for Statistical and Translational Genetics RIKEN Center for Integrative Medical Sciences Yokohama Japan Clinical Research Center Shizuoka General Hospital Shizuoka Japan The Department of Applied Genetics The School of Pharmaceutical Sciences University of Shizuoka Shizuoka Japan. Department of Medical Research China Medical University Hospital Taichung 404327 Taiwan. Department of Medical Research China Medical University Hospital China Medical University Taichung 404327 Taiwan. Graduate Institute of Biomedical Informatics College of Medical Science and Technology Taipei Medical University Taipei Taiwan. School of Chinese Medicine China Medical University Taichung Taiwan Department of Biotechnology and Bioinformatics Asia University Taichung Taiwan. Electronic address: d0704@mail.cmuh.org.tw.

Immunoglobulin E (IgE) synthessis is highly related to a variety of atopic diseases, and several genome-wide association studies (GWASs) have demonstrated the association between genes and IgE level. In this study, we conducted the largest genome-wide association study of IgE involving a Taiwanese Han population. Eight independent variants exhibited genome-wide significance. Among them, an intronic SNP of CD28, rs1181388, and an intergenic SNP, rs1002957030, on 11q23.2 were identified as novel signals for IgE. Seven of the loci were replicated successfully in a meta-analysis using data on Japanese population. Among all the human leukocyte antigen (HLA) regions, HLA-DQA1*03:02 - HLA-DQB1*03:03 was the most significant haplotype (OR = 1.25, SE = 0.02, FDR = 1.6 × 10), corresponding to HLA-DQA1 Asp160 and HLA-DQB1 Leu87 amino acid residues. The genetic correlation showed significance between IgE and allergic diseases including asthma, atopic dermatitis, and pollinosis. IgE PRS was significantly correlated with total IgE levels. Furthermore, the top decile IgE polygenic risk score (PRS) group had the highest risk of asthma for the Taiwan Biobank and Biobank Japan cohorts. IgE PRS may be used to aid in predicting the occurrence of allergic reactions before symptoms occur and biomarkers are detectable. Our study provided a more comprehensive understanding of the impact of genomic variants, including complex HLA alleles, on serum IgE levels.

关键词： Allergy genome-wide association study human leukocyte antigen immunoglobulin E

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Caffeic acid phenethyl ester suppresses EGFR/FAK/Akt signaling, migration, and tumor growth of prostate cancer cells

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Phytomedicine 2023年 116卷

作者： Jen-Chih Tseng Bi-Juan Wang Ya-Pei Wang Ying-Yu Kuo Jen-Kun Chen Tzyh-Chyuan Hour Li-Kuo Kuo Po-Jen Hsiao Chien-Chih Yeh Cheng-Li Kao Li-Jane Shih Chih-Pin Chuu Institute of Cellular and System Medicine National Health Research Institutes Miaoli County 35053 Taiwan Immunology Research Center National Health Research Institutes Miaoli County 35053 Taiwan Institute of Biomedical Engineering and Nanomedicine National Health Research Institutes Miaoli County 35053 Taiwan Neuroscience Research Center Kaohsiung Medical University Kaohsiung 80737 Taiwan Department of Biochemistry School of Medicine Kaohsiung Medical University Kaohsiung 80737 Taiwan Department of Medical Research Kaohsiung Medical University Hospital Kaohsiung 80737 Taiwan Division of Pulmonary and Critical Care Medicine Department of Internal Medicine Mackay Memorial Hospital Taipei City 104217 Taiwan Department of Nursing Mackay Medical College Taipei City Taiwan Division of Nephrology Department of Internal Medicine Taoyuan Armed Forces General Hospital Taoyuan 325 Taiwan Division of Nephrology Department of Internal Medicine Tri-Service General Hospital National Defense Medical Center Taipei 114 Taiwan Department of Education and Medical Research Taoyuan Armed Forces General Hospital Taoyuan Taiwan Division of Colon and Rectal Surgery Department of Surgery Tri-Service General Hospital National Defense Medical Center Taipei Taiwan Division of Urology Departments of Surgery Tri-Service General Hospital National Defense Medical Center Taipei Taiwan Division of Urology Department of Surgery Taoyuan Armed Forces General Hospital Taoyuan Taiwan Graduate Institute of Medical Science National Defense Medical Center Taipei 114 Taiwan Department of Life Sciences National Central University Taoyuan 32031 Taiwan PhD Program for Aging and Graduate Institute of Basic Medical Science China Medical University Taichung City 40402 Taiwan Biotechnology Center National Chung Hsing University Taichung City 40227 Taiwan

Background Epidermal growth factor receptor (EGFR) is upregulated in prostate cancer (PCa). However, suppression of EGFR did not improve the patient outcome, possibly due to the activation of PI3K/Akt signaling in PCa. Compounds able to suppress both PI3K/Akt and EGFR signaling may be effective for treating advanced PCa. Purpose We examined if caffeic acid phenethyl ester (CAPE) simultaneously suppresses the EGFR and Akt signaling, migration and tumor growth in PCa cells. Methods Wound healing assay, transwell migration assay and xenograft mice model were used to determine the effects of CAPE on migration and proliferation of PCa cells. Western blot, immunoprecipitation, and immunohistochemistry staining were performed to determine the effects of CAPE on EGFR and Akt signaling. Results CAPE treatment decreased the gene expression of HRAS, RAF1, AKT2, GSK3A , and EGF and the protein expression of phospho-EGFR (Y845, Y1069, Y1148, Y1173), phospho-FAK, Akt, and ERK1/2 in PCa cells. CAPE treatment inhibited the EGF-induced migration of PCa cells. Combined treatment of CAPE with EGFR inhibitor gefitinib showed additive inhibition on migration and proliferation of PCa cells. Injection of CAPE (15 mg/kg/3 days) for 14 days suppressed the tumor growth of prostate xenografts in nude mice as well as suppressed the levels of Ki67, phospho-EGFR Y845, MMP-9, phospho-Akt S473, phospho-Akt T308, Ras, and Raf-1 in prostate xenografts. Conclusions Our study suggested that CAPE can simultaneously suppress the EGFR and Akt signaling in PCa cells and is a potential therapeutic agent for advanced PCa.

关键词： Prostate cancer Caffeic acid phenethyl ester Metastasis Epidermal growth factor receptor Fak Akt CAPE caffeic acid phenethyl ester CRPC castration-resistant prostate cancer EGFR epidermal growth factor receptor EMT epithelial-mesenchymal transition GAPDH glyceraldehyde-3-phosphate dehydrogenase mTOR mammalian target of rapamycin PCa prostate cancer PI3K phosphoinositide 3-kinase PSA prostate specific antigen PSMA prostate specific-membrane antigen PTEN phosphatase and tensin homolog

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Patterns of somatic structural variation in human cancer genomes (vol 578, pg 112, 2020)

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NATURE 2023年第7948期614卷 E38-E38页

作者： Li, Yilong Roberts, Nicola D. Wala, Jeremiah A. Shapira, Ofer Schumacher, Steven E. Kumar, Kiran Khurana, Ekta Waszak, Sebastian Korbel, Jan O. Haber, James E. Imielinski, Marcin Weischenfeldt, Joachim Beroukhim, Rameen Campbell, Peter J. Cancer Genome Project Wellcome Trust Sanger Institute Hinxton UK Totient Inc Cambridge MA USA Wellcome Sanger Institute Wellcome Genome Campus Hinxton UK Department of Haematology University of Cambridge Cambridge UK Cambridge University Hospitals NHS Foundation Trust Cambridge UK Korea Advanced Institute of Science and Technology Daejeon South Korea Department of Zoology Genetics and Physical Anthropology University of Santiago de Compostela Santiago de Compostela Spain Centre for Research in Molecular Medicine and Chronic Diseases (CIMUS) University of Santiago de Compostela Santiago de Compostela Spain The Biomedical Research Centre (CINBIO) University of Vigo Vigo Spain Centre for Research in Molecular Medicine and Chronic Diseases (CiMUS) Universidade de Santiago de Compostela Santiago de Compostela Spain Department of Zoology Genetics and Physical Anthropology (CiMUS) Universidade de Santiago de Compostela Santiago de Compostela Spain The Biomedical Research Centre (CINBIO) Universidade de Vigo Vigo Spain The Broad Institute of Harvard and MIT Cambridge MA USA Bioinformatics and Integrative Genomics Harvard University Cambridge MA USA Department of Cancer Biology Dana-Farber Cancer Institute Boston MA USA Broad Institute of MIT and Harvard Cambridge MA USA Department of Medical Oncology Dana-Farber Cancer Institute Boston MA USA Harvard Medical School Boston MA USA Massachusetts General Hospital Center for Cancer Research Charlestown MA USA Dana-Farber Cancer Institute Boston MA USA Department of Biostatistics and Computational Biology Dana-Farber Cancer Institute and Harvard Medical School Boston MA USA Weill Cornell Medical College New York NY USA Department of Physiology and Biophysics Weill Cornell Medicine New York NY USA Institute for Computational Biomedicine Weill Cornell Medicine New York NY USA Controlled Department and Institution New York NY USA Englander Institute for Precision Medicine Weill Cornell Medicine Ne

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Author Correction: Genomic footprints of activated telomere maintenance mechanisms in cancer (Dec, 10.1038/s41467-019-13824-9, 2022)

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NATURE COMMUNICATIONS 2022年第1期13卷 1-1页

作者： Sieverling, Lina Hong, Chen Koser, Sandra D. Ginsbach, Philip Kleinheinz, Kortine Hutter, Barbara Braun, Delia M. Cortes-Ciriano, Isidro Xi, Ruibin Kabbe, Rolf Park, Peter J. Eils, Roland Schlesner, Matthias Brors, Benedikt Rippe, Karsten Jones, David T. W. Feuerbach, Lars Division of Applied Bioinformatics German Cancer Research Center (DKFZ) 69120 Heidelberg Germany Faculty of Biosciences Heidelberg University 69120 Heidelberg Germany Division of Applied Bioinformatics German Cancer Research Center (DKFZ) Heidelberg Germany Faculty of Biosciences Heidelberg University Heidelberg Germany Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ) 69120 Heidelberg Germany Department for Bioinformatics and Functional Genomics Institute for Pharmacy and Molecular Biotechnology (IPMB) and BioQuant 69120 Heidelberg Germany Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ) Heidelberg Germany Institute of Pharmacy and Molecular Biotechnology and BioQuant Heidelberg University Heidelberg Germany German Cancer Consortium (DKTK) Heidelberg Germany National Center for Tumor Diseases (NCT) Heidelberg Heidelberg Germany Heidelberg Center for Personalized Oncology (DKFZ-HIPO) German Cancer Research Center (DKFZ) Heidelberg Germany German Cancer Consortium (DKTK) German Cancer Research Center (DKFZ) Heidelberg Germany Division of Chromatin Networks German Cancer Research Center (DKFZ) and BioQuant 69120 Heidelberg Germany Department of Biomedical Informatics Harvard Medical School Boston Massachusetts 02115 USA Department of Chemistry Centre for Molecular Science Informatics University of Cambridge Cambridge CB2 1EW UK Ludwig Center at Harvard Medical School Boston Massachusetts 02115 USA Department of Biomedical Informatics Harvard Medical School Boston MA USA Department of Chemistry Centre for Molecular Science Informatics University of Cambridge Cambridge UK Ludwig Center at Harvard Medical School Boston MA USA School of Mathematical Sciences and Center for Statistical Science Peking University Beijing 100871 China Heidelberg University Heidelberg Germany New BIH Digital Health Center Berlin Institute of Health (BIH) and Charité - Universitätsmedizin Berlin Berlin Germany Bioi

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