An miRNA fingerprint using neural-enriched extracellular vesicles from blood plasma: towards a biomarker for amyotrophic lateral sclerosis/motor neuron disease DOI Creative Commons
Sandra Anne Banack, Rachael A. Dunlop, Paul Alan Cox

и другие.

Open Biology, Год журнала: 2020, Номер 10(6)

Опубликована: Июнь 1, 2020

Biomarkers for amyotrophic lateral sclerosis/motor neuron disease (ALS/MND) are currently not clinically available diagnosis or analysis of progression. If identified, biomarkers could improve patient outcomes by enabling early intervention and assist in the determination treatment efficacy. We hypothesized that neural-enriched extracellular vesicles provide microRNA (miRNA) fingerprints with unequivocal signatures neurodegeneration. Using blood plasma from ALS/MND patients controls, we extracted vesicle fractions conducted next-generation sequencing qPCR miRNA components transcriptome. here report eight sequences which significantly distinguish controls a replicated experiment using second cohort controls. samples may yield unique insights into mechanisms neurodegeneration ALS/MND.

Язык: Английский

<p>Cancer-Derived Exosomes: Their Role in Cancer Biology and Biomarker Development</p> DOI Creative Commons
Victor C. Kok, Cheng‐Chia Yu

International Journal of Nanomedicine, Год журнала: 2020, Номер Volume 15, С. 8019 - 8036

Опубликована: Окт. 1, 2020

Abstract: Exosomes are a subset of tiny extracellular vesicles manufactured by all cells and present in body fluids. They produced actively tumor cells, which released utilized to facilitate growth. Their characteristics enable them assist major cancer hallmarks, leveraged fostering growth spread while implementing ways escape elimination from the host environment. This review updates on latest progress roles cancer-derived exosomes, 30– 100 nm size, deregulating paracrine trafficking microenvironment circulation. Thus, exosomes being exploited diagnostic biomarker development, with its potential clinical applications as therapeutic targets exosome‐based nanoparticle drug delivery strategies for therapy. Ongoing studies were retrieved PubMed ® Scopus database ClinicalTrials.gov registry review, highlighting how entirely different cell lines rely genetic information carried their homotypic heterotypic intercellular communications favor proliferation invasion, establishing pre-metastatic niche welcoming cells’ arrival. We will elaborate tumor-derived proliferation, metastasis hematopoietic (leukemia myeloma), epithelial (breast cancer), mesenchymal (soft tissue sarcoma osteosarcoma) cancers. Cancer-derived exosomal is observed several types liquid or solid tumors, confirming role hallmark enabler. enriched signals arising characteristic DNA, RNA, microRNA, lncRNA, along specific gene expression profiles, protein, lipid composition cargo shed into blood, saliva, urine, ascites, cervicovaginal lavage, studied diagnostic, prognostic, predictive biomarker. reveal research efforts exploiting use nanoparticles improve overall capability clinic. Keywords: tumor-released carcinoma-associated fibroblasts, exosome cargo, exosome-induced chemoresistance, hallmarks cancer, tumor-stromal

Язык: Английский

Процитировано

322

Roles and mechanisms of exosomal non-coding RNAs in human health and diseases DOI Creative Commons
Chen Li, Yu‐Qing Ni, Hui Xu

и другие.

Signal Transduction and Targeted Therapy, Год журнала: 2021, Номер 6(1)

Опубликована: Ноя. 10, 2021

Exosomes play a role as mediators of cell-to-cell communication, thus exhibiting pleiotropic activities to homeostasis regulation. Exosomal non-coding RNAs (ncRNAs), mainly microRNAs (miRNAs), long (lncRNAs), and circular (circRNAs), are closely related variety biological functional aspects human health. When the exosomal ncRNAs undergo tissue-specific changes due diverse internal or external disorders, they can cause tissue dysfunction, aging, diseases. In this review, we comprehensively discuss underlying regulatory mechanisms exosomes in addition, explore current knowledge on roles miRNAs, lncRNAs, circRNAs health diseases, including cancers, metabolic neurodegenerative cardiovascular autoimmune infectious determine their potential implication biomarker identification therapeutic exploration.

Язык: Английский

Процитировано

282

Biomarkers in Stress Related Diseases/Disorders: Diagnostic, Prognostic, and Therapeutic Values DOI Creative Commons
Kuldeep Dhama,

Shyma K. Latheef,

Maryam Dadar

и другие.

Frontiers in Molecular Biosciences, Год журнала: 2019, Номер 6

Опубликована: Окт. 18, 2019

Various internal and external factors negatively affect the homeostatic equilibrium of organisms at molecular to whole-body level, inducing so-called state 'stress'. Stress affects an organism's welfare status induces energy-consuming mechanisms combat subsequent ill effects; thus, individual may be immunocompromised, making them vulnerable pathogens. The information presented here has been extensively reviewed, compiled analyzed from authenticated published resources available on Medline, Pubmed, Pubmed Central, Science Direct, other scientific databases. levels can monitored by quantitative qualitative measurement biomarkers. Prominent markers stress include thermal like heat shock proteins (HSPs), innate immune Acute Phase Proteins (APPs), oxidative markers, chemical secretions in saliva urine. In addition, biomarkers are thought play critical roles prognosis stress-related diseases disorders, therapy guidance. Moreover, different components have identified as potent mediators cardiovascular, central nervous system, hepatic, nephrological which also employed evaluate these conditions precisely, but with stringent validation specificity. Considerable advances made detection, quantitation, application present review describes current progress identifying biomarkers, their prognostic therapeutic values.

Язык: Английский

Процитировано

262

Tumorigenesis, diagnosis, and therapeutic potential of exosomes in liver cancer DOI Creative Commons
Hongbo Wang, Zaiming Lu, Xiangxuan Zhao

и другие.

Journal of Hematology & Oncology, Год журнала: 2019, Номер 12(1)

Опубликована: Дек. 1, 2019

Abstract Hepatocellular carcinoma (HCC, also called primary liver cancer) is one of the most fatal cancers in world. Due to insidiousness onset HCC and lack effective treatment methods, prognosis extremely poor, 5-year average survival rate less than 10%. Exosomes are nano-sized microvesicle contain various components such as nucleic acids, proteins, lipids. important carriers for signal transmission or transportation material from cell between cells tissues. In recent years, exosomes have been considered potential therapeutic targets HCC. A large number reports indicate that play a key role establishment an microenvironment, well development, progression, invasion, metastasis, even diagnosis, treatment, However, exact molecular mechanisms roles these processes remain unclear. We believe elucidation regulatory mechanism HCC-related its signaling pathway analysis clinical applications diagnosis can provide useful clues future regimens This article discusses summarizes research progress their applications.

Язык: Английский

Процитировано

236

Current Progresses of Exosomes as Cancer Diagnostic and Prognostic Biomarkers DOI Creative Commons
Tao Huang, Chu‐Xia Deng

International Journal of Biological Sciences, Год журнала: 2018, Номер 15(1), С. 1 - 11

Опубликована: Дек. 19, 2018

Cancer related exosomes are nano-size membrane vesicles that play important roles in tumor microenvironment.Emerging evidence indicates can load unique cargoes, including proteins and nucleic acids reflect the condition of tumor.Therefore, being used as diagnostic prognostic biomarkers for various cancers.In this review, we describe current progresses cancer exosomes, their biogenesis, molecular contents, biological functions, sources where they derived from, methods detection.We will also discuss exosomal utilization them early diagnosis prognostics cancer.

Язык: Английский

Процитировано

213

Circulating biomarkers in the diagnosis and management of hepatocellular carcinoma DOI
Philip J. Johnson, Qing Zhou,

Doan Y Dao

и другие.

Nature Reviews Gastroenterology & Hepatology, Год журнала: 2022, Номер 19(10), С. 670 - 681

Опубликована: Июнь 8, 2022

Язык: Английский

Процитировано

210

Current Status and Perspective Biomarkers in AFP Negative HCC: Towards Screening for and Diagnosing Hepatocellular Carcinoma at an Earlier Stage DOI
Ping Luo,

Sanyun Wu,

Yalan Yu

и другие.

Pathology & Oncology Research, Год журнала: 2019, Номер 26(2), С. 599 - 603

Опубликована: Янв. 19, 2019

Язык: Английский

Процитировано

197

Emerging Function and Clinical Values of Exosomal MicroRNAs in Cancer DOI Creative Commons
Man Wang, Fei Yu, Han Ding

и другие.

Molecular Therapy — Nucleic Acids, Год журнала: 2019, Номер 16, С. 791 - 804

Опубликована: Май 15, 2019

Exosomes are a subset of membrane-bound extracellular vesicles with diameters ranging from 30 to 100 nm. enclose variety molecules, such as lipids, proteins, and non-coding RNAs. In the past decades, microRNAs (miRNAs) have attracted great attention in cancer research, they play an important role occurrence development cancer. Increasing evidence indicates that tumor cells communicate not only other but also present microenvironment via secretion transfer exosomal miRNAs. More importantly, miRNAs found serve signaling molecules regulate growth, angiogenesis, metastasis, sensitivity chemotherapy, immune evasion. Deregulated expression is early event carcinogenesis may reflect malignant characteristics Owing wide existence high stability body fluids, represent novel class non-invasive biomarkers for this review, we highlight recent advances on functional pathogenesis. We discuss potential clinical utility exosome-shuttled diagnosis treatment 30- 100-nm endosomal origin, comprising lipid bilayer bioactive nucleic acids, proteins.1Abak A. Abhari Rahimzadeh S. cancer: small vesicular transporters progression therapeutics.PeerJ. 2018; 6: e4763Crossref PubMed Scopus (6) Google Scholar released all cell types, including epithelial cells, cells.2Pap E. Pállinger Falus The membrane tumorigenesis.Crit. Rev. Oncol. Hematol. 2011; 79: 213-223Crossref (0) Scholar, 3van Niel G. Raposo Candalh C. Boussac M. Hershberg R. Cerf-Bensussan N. Heyman Intestinal secrete exosome-like vesicles.Gastroenterology. 2001; 121: 337-349Abstract Full Text PDF 4Blanchard Lankar D. Faure F. Regnault Dumont Hivroz TCR activation human T induces production exosomes bearing TCR/CD3/zeta complex.J. Immunol. 2002; 168: 3235-3241Crossref Notably, excessive amounts compared normal proliferating cells.5Kharaziha P. Ceder Li Q. Panaretakis T. 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Lung Cancer. 2009; 42-46Abstract (1020) demonstrating ideal summarize current knowledge progression. applications practice. generated both pathological fluids.31Brinton L.T. Sloane H.S. Kester Kelly K.A. Formation cancer.Cell. 72: 659-671Crossref (154) originate compartment.32Gruenberg van der Goot F.G. pathogen entry compartments.Nat. 2006; 7: 495-504Crossref (269) biogenesis involves two steps.33Kowal Tkach Biogenesis exosomes.Curr. 2014; 29: 116-125Crossref (1073) First, internalization leads formation endosomes (Figure 1). intraluminal (ILVs) then formed inward invagination membranes, resulting MVBs. During process, cytosolic sorted ILVs. Upon membrane, ILVs milieu. Some factors exosome biogenesis. sorting complexes required transport (ESCRTs) essential MVB biogenesis, which cargo coupled detachment ILVs.34Wollert Hurley Molecular ESCRT complexes.Nature. 464: 864-869Crossref (504) ESCRT-0 responsible assembly gathering cargoes. ESCRT-I -II harbor various membrane-binding sites, membrane. capable bud, cargoes confined. ESCRT-II recruits ESCRT-III subunits, vacuolar protein sorting-associated 20 (Vps20) eukaryotic sucrose non-fermenting 7 (Snf7), neck bud. complex directs scission cytoplasmic side Following scission, entrapped while ESCR-III persists outside remaining until it recycled. Moreover, accessory ALG-2-interacting X (ALIX) susceptibility gene 101 (TSG101), packaging ALIX encloses enter internalized vesicle formation.35Baietti M.F. Z. Mortier Melchior Degeest Geeraerts Ivarsson Depoortere Coomans Vermeiren et al.Syndecan-syntenin-ALIX regulates exosomes.Nat. 677-685Crossref (1022) complex, ILVs.36Hurley Odorizzi Get bus ALIX.Nat. 654-655Crossref (145) TSG101, component machinery, epidermal growth factor (EGF)-stimulated formation.37Razi Futter C.E. Distinct Tsg101 Hrs vesiculation.Mol. 3469-3483Crossref (191) Accordingly, depletion TSG101 suppress formation. Members Rab GTPase family (e.g., Rab27a Rab27b) mediate trafficking site membrane.38Bobrie Krumeich Reyal Recchi Moita L.F. Seabra Ostrowski supports exosome-dependent -independent modify progression.Cancer Res. 4920-4930Crossref (399) 39Ostrowski Carmo N.B. Fanget I. Savina C.F. Schauer Hume A.N. Freitas R.P. al.Rab27a Rab27b control different steps pathway.Nat. 19-30Crossref (1516) requires contractile machinery able draw opposing membranes together prior shearing connection releasing milieu.40Cocucci Racchetti Meldolesi Shedding microvesicles: artefacts no more.Trends 19: 43-51Abstract (1360) Soluble N-ethylmaleimide-sensitive attachment receptor (SNARE) facilitate membrane.41Südhof T.C. Rothman J.E. Membrane fusion: grappling SNARE SM proteins.Science. 323: 474-477Crossref (1404) represents focus investigation would enrich our underlying A incorporated exosomes, miRNAs, DNAs, RNAs, proteins. 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Yi Hudson R.S. Howe T.M. Petrocca Wallace T.A. C.G. Volinia al.Genomic messenger RNA reveals deregulated prostate cancer.Cancer 68: 6162-6170Crossref (594) miR-142-3p, miR-150, miR-451 were enriched parent preferentially packaged exosomes.51Guduric-Fuchs O'Connor Camp O'Neill C.L. Medina R.J. Simpson D.A. Selective vesicle-mediated export overlapping set types.BMC Genomics. 13: 357Crossref (363) Likewise, members let-7 more abundant derived gastric (GC) than those cells.52Ohshima Inoue Fujiwara Hatakeyama Kanto Watanabe Muramatsu Fukuda Ogura Yamaguchi Mochizuki Let-7 selectively environment metastatic line.PLoS ONE. 5: e13247Crossref (484) Remarkably, some miR-21, let-7f, miR-20b, miR-30e-3p) exhibited levels patients healthy controls.53Skog Würdinger Rijn Meijer D.H. Gainche Sena-Esteves Curry Jr., W.T. Carter B.S. Krichevsky Breakefield X.O. Glioblastoma microvesicles proteins tumour provide biomarkers.Nat. 1470-1476Crossref (3541) 54Silva García Zaballos Á. Provencio Lombardía Almonacid Domínguez Peña Diaz al.Vesicle-related nonsmall correlation survival.Eur. Respir. 617-623Crossref (219) adopt specific direct loading leading selective encapsulation cell-secreted exosomes. Four pathways proposed 2). neural sphingomyelinase 2 (nSMase2)-dependent pathway was guide nSMase2 first molecule exosomes.55Zhang Guo Yao Mi trafficking, sorting, function.Genomics Proteomics Bioinformatics. 17-24Crossref (1050) Overexpression caused increase abundance miRNAs.56Kosaka Iguchi Hagiwara Yoshioka Takeshita Ochiya Neutral angiogenic Chem. 288: 10849-10859Abstract (497) contrast, inhibition decreased second sumoylated heterogeneous nuclear ribonucleoprotein (hnRNP)-dependent pathway. Three hnRNP (hnRNPA2B1, hnRNPA1, hnRNPC) bound induced exosomes.57Villarroya-Beltri Gutiérrez-Vázquez Sánchez-Cabo Pérez-Hernández Vázquez Martin-Cofreces Martinez-Herrera D.J. Pascual-Montano Sánchez-Madrid Sumoylated hnRNPA2B1 controls motifs.Nat. Commun. 4: 2980Crossref (1124) Specially, controlled assortment recognizing GGAG motif part sequences. third depends end miRNA. sequence might contain signal contributed guiding incorporation exosomes.58Koppers-Lalic Hackenberg Bijnsdorp I.V. Eijndhoven M.A.J. Sadek Sie Zini Middeldorp Ylstra Menezes R.X. al.Nontemplated nucleotide additions distinguish composition exosomes.Cell Rep. 8: 1649-1658Abstract (371) last mediated miRNA-induced silencing (miRISC). primary miRISC co-localize MVBs.59Gibbings Ciaudo Erhardt Voinnet O. Multivesicular associate effector modulate activity.Nat. 1143-1149Crossref (787) blockade turnover lysosomes resulted accumulation miRISCs, suppression loss relieved miRNA-mediated silencing.60Lee Y.S. Pressman Andress A.P. White J.L. Cassidy Lubell Lim Cho I.S. al.Silencing linked trafficking.Nat. 1150-1156Crossref (270) It reported activation-dependent changes abundance.61Squadrito Baer Burdet Maderna Gilfillan G.D. Lyle Ibberson De Palma Endogenous acceptor cells.Cell 1432-1446Abstract (417) Artificially elevating benefited enrichment Argonaute (Ago2), RISC, implicated Knockout Ago2 could reduce miR-451.51Guduric-Fuchs Collectively, certain sequences favor uptake Nevertheless, remain unclear deserve further investigation. shown exert multifaceted effects progression, regulation angiogenesis domination host responses, manipulation chemoresistance, 3). Proliferation aspect commonly manifested cycle-related contributing metastasis. cancer-secreted proliferation targeting cycle-associated pathways. miR-200b transmitted colorectal (CRC) promoted recipient lowering p27 expression.62Zhang Xing promotes TGF-β1 exposure.Biomed. Pharmacother. 106: 1135-1143Crossref (2) miR-6869-5p depress CRC inhibit inflammatory (interleukin-6 [IL-6] necrosis alpha [TNF-α]) blocking Toll-like 4 (TLR4)/nuclear κB (NF-κB)-signaling pathway.63Yan Jin Duan Xu MicroRNA-6869-5p acts suppressor TLR4/NF-κB cancer.J. 233: 6660-6668Crossref Inhibition oncogenic miR-21 suppressed migration hepatocellular carcinoma (HCC) cells.64Liang He Miao Wu Gan Sphk2 RNAi nanoparticles downregulating microRNA.J. Control. Release. 286: 348-357Crossref (1) miR-9-3p restrained HCC directly fibroblast 5 (HBGF-5).65Tang Zhu Yang W.H. Xiong L.K. D.L. suppresses HBGF-5 biomarker carcinoma.Minerva 109: 15-23PubMed miR-1246, transferred non-malignant cells.66Li X.J. Ren Z.J. Tang Yu MiR-1246 Promotes Proliferation, Invasion Drug Resistance Targeting CCNG2 Breast Cancer.Cell. 44: 1741-1748Crossref (167) miR-1246 migration, resistance cyclin-G2 (CCNG2). miR-193a impeded cycle exerted inhibitory effect colon 1 (Caprin1).67Teng Hu Mu Samykutty Zhuang Deng Kumar Merchant al.MVP-mediated progression.Nat. 14448Crossref (260) orchestrate apoptotic cells. For instance, miR-128 reduced Bcl-2-associated (Bax) cells.68Wei Cui Shikonin Inhibits Cells Reducing Tumor-Derived Exosomes.Molecules. 21: 777Crossref (21) miR-373 repressed estrogen (ER) inhibited apoptosis cells.69Eichelser Stückrath Müller Milde-Langosch Wikman Pantel Schwarzenbach Increased serum circulating microRNA-373 receptor-negative patients.Oncotarget. 9650-9663Crossref adipose mesenchymal stem (hAMSC)-derived induce (OC) upregulating (Bax, caspase 3, 9) anti-apoptotic Bcl-2.70Reza A.M.M.T. Y.J. Yasuda exosomal-miRNAs anti-proliferation signalling A2780 SKOV-3 cells.Sci. 38498Crossref (31) miR-101 GC myeloid leukemia-1 (Mcl-1).71Imamura Komatsu Ichikawa Miyamae Okajima Ohashi Kiuchi Nishibeppu Kosuga Konishi al.Low cancer.Oncotarget. 106538-106550Crossref (9) epithelial-mesenchymal transition (EMT), vital process invasion characterized

Язык: Английский

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174

Exosomes and cancer - Diagnostic and prognostic biomarkers and therapeutic vehicle DOI Creative Commons
Xia Wang, Lü Tian,

Jingyi Lu

и другие.

Oncogenesis, Год журнала: 2022, Номер 11(1)

Опубликована: Сен. 15, 2022

Abstract Exosomes belong to a subpopulation of extracellular vesicles secreted by the dynamic multistep endocytosis process and carry diverse functional molecular cargoes, including proteins, lipids, nucleic acids (DNA, messenger noncoding RNA), metabolites promote intercellular communication. Proteins RNA are among most abundant contents in exosomes; they have biological functions selectively packaged into exosomes. derived from tumor, stromal immune cells contribute multiple stages cancer progression as well resistance therapy. In this review, we will discuss biogenesis exosomes their roles development. Since specific within originate origin, property allows function valuable biomarkers. We also potential use diagnostic prognostic biomarkers or predictors for different therapeutic strategies cancers. Furthermore, applications direct targets engineered vehicles drugs an important field exosome study. Better understanding biology may pave way promising exosome-based clinical applications.

Язык: Английский

Процитировано

164

Extracellular vesicles as biomarkers in liver diseases: A clinician's point of view DOI Creative Commons
Sara Thietart, Pierre‐Emmanuel Rautou

Journal of Hepatology, Год журнала: 2020, Номер 73(6), С. 1507 - 1525

Опубликована: Июль 15, 2020

Язык: Английский

Процитировано

151