Emerging Frontiers in Neuro-Oncology: Insights into Extracellular Vesicle-Driven Tumor Mechanisms and Nanotherapeutic Strategies
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Brain tumors encompass a heterogeneous group of neoplasms, including primary and secondary metastatic lesions, with glioblastoma multiforme (GBM) representing the most aggressive primary malignancy. Despite advancements in surgical resection, radiotherapy, and chemotherapy, the prognosis for GBM remains poor due to its infiltrative nature, tumor heterogeneity and resistance mechanisms. Emerging diagnostic tools, such as liquid biopsies, and therapeutic strategies leveraging extracellular vesicles (EVs) are reshaping the field of neuro-oncology. EVs, lipid bilayer-enclosed particles secreted by cells, carry oncogenic cargo such as microRNAs and molecular chaperones, influencing tumor progression, immune evasion, and therapy resistance. Recent research highlights their potential as biomarkers for early diagnosis and vehicles for targeted drug delivery across the blood–brain barrier (BBB). EV-based nanotherapeutics show promise in improving treatment precision, reducing systemic toxicity, and advancing precision medicine in brain tumor management. However, challenges related to EV heterogeneity, cargo-loading efficiency, and large-scale production must be addressed to fully realize their therapeutic potential. This review explores the multifaceted roles of EVs in brain tumors, emphasizing their diagnostic, prognostic, and therapeutic applications.
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Extracellular vesicles regulate cell migration in several cancer types, including glioblastoma.
“In this context, extracellular vesicles (EVs) have emerged as important mediators, regulating cell migration in several cancer types, including GB.”
From Optimized Wound Healing Assay to Study Extracellular Vesicle-Driven Glioblastoma Cell Migration (2026) · cites this paper as [31]
Section 4.1 (page unavailable) says GBM-derived EVs enhance invasiveness, supporting a role in glioblastoma cell migration. The passages found do not establish that EVs regulate cell migration in several cancer types; that broader part of the claim is unsupported by our copy. (LLM, conf=0.82)
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- [1]Vitale A.M. Santonocito R. Vergilio G. Marino Gammazza A. Campanella C. Conway de Macario E. Bucchieri F. Macario A.J.L. Caruso Bavisotto C. Brain Tumor-Derived Extracellular Vesicles as Carriers of Disease Markers: Molecular Chaperones and MicroRNAs Appl. Sci. 2020 10 6961 10.3390/app10196961 · DOI
- [2]Lapointe S. Perry A. Butowski N.A. Primary Brain Tumours in Adults Lancet 2018 392 432 446 10.1016/S0140-6736(18)30990-5 30060998 · DOI
- [3]Ostrom Q.T. Price M. Neff C. Cioffi G. Waite K.A. Kruchko C. Barnholtz-Sloan J.S. CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2016–2020 Neuro Oncol. 2023 25 iv1 iv99 10.1093/neuonc/noad149 37793125 PMC10550277 · DOI · Paper page
- [4]Bray F. Laversanne M. Sung H. Ferlay J. Siegel R.L. Soerjomataram I. Jemal A. Global Cancer Statistics 2022: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries CA A Cancer J. Clin. 2024 74 229 263 10.3322/caac.21834 38572751 · DOI · Paper page
- [5]Huang C.-H. Chen C.-J. Chen P.-N. Wang S.-S. Chou Y.-E. Hung S.-C. Yang S.-F. Impacts of AURKA Genetic Polymorphism on Urothelial Cell Carcinoma Development J. Cancer 2019 10 1370 1374 10.7150/jca.30014 31031846 PMC6485228 · DOI
- [6]Lane R.E. Korbie D. Hill M.M. Trau M. Extracellular Vesicles as Circulating Cancer Biomarkers: Opportunities and Challenges Clin. Transl. Med. 2018 7 14 10.1186/s40169-018-0192-7 29855735 PMC5981152 · DOI
- [7]Yadav D. Malviya R. Exploring Potential of Exosomes Drug Delivery System in the Treatment of Cancer: Advances and Prospective Med. Drug Discov. 2023 20 100163 10.1016/j.medidd.2023.100163 · DOI
- [8]Melo S.A. Sugimoto H. O’Connell J.T. Kato N. Villanueva A. Vidal A. Qiu L. Vitkin E. Perelman L.T. Melo C.A. Cancer Exosomes Perform Cell-Independent MicroRNA Biogenesis and Promote Tumorigenesis Cancer Cell 2014 26 707 10.1016/j.ccell.2014.09.005 25446899 PMC4254633 · DOI
- [9]Huang Z. Keramat S. Izadirad M. Chen Z.-S. Soukhtanloo M. The Potential Role of Exosomes in the Treatment of Brain Tumors, Recent Updates and Advances Front. Oncol. 2022 12 869929 10.3389/fonc.2022.869929 35371984 PMC8968044 · DOI
- [10]Kleihues P. Burger P.C. Scheithauer B.W. The New WHO Classification of Brain Tumours Brain Pathol. 1993 3 255 268 10.1111/j.1750-3639.1993.tb00752.x 8293185 · DOI
- [11]Kleihues P. Louis D.N. Scheithauer B.W. Rorke L.B. Reifenberger G. Burger P.C. Cavenee W.K. The WHO Classification of Tumors of the Nervous System J. Neuropathol. Exp. Neurol. 2002 61 215 225 10.1093/jnen/61.3.215 11895036 · DOI
- [12]Louis D.N. Ohgaki H. Wiestler O.D. Cavenee W.K. Burger P.C. Jouvet A. Scheithauer B.W. Kleihues P. The 2007 WHO Classification of Tumours of the Central Nervous System Acta Neuropathol. 2007 114 97 109 10.1007/s00401-007-0243-4 17618441 PMC1929165 · DOI
- [13]Louis D.N. Perry A. Reifenberger G. von Deimling A. Figarella-Branger D. Cavenee W.K. Ohgaki H. Wiestler O.D. Kleihues P. Ellison D.W. The 2016 World Health Organization Classification of Tumors of the Central Nervous System: A Summary Acta Neuropathol. 2016 131 803 820 10.1007/s00401-016-1545-1 27157931 · DOI
- [14]Ostrom Q.T. Gittleman H. Liao P. Rouse C. Chen Y. Dowling J. Wolinsky Y. Kruchko C. Barnholtz-Sloan J. CBTRUS Statistical Report: Primary Brain and Central Nervous System Tumors Diagnosed in the United States in 2007–2011 Neuro Oncol. 2014 16 iv1 iv63 10.1093/neuonc/nou223 25304271 PMC4193675 · DOI
- [15]Ostrom Q.T. Patil N. Cioffi G. Waite K. Kruchko C. Barnholtz-Sloan J.S. CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2013–2017 Neuro Oncol. 2020 22 iv1 iv96 10.1093/neuonc/noaa200 33123732 PMC7596247 · DOI
- [16]Perkins A. Liu G. Primary Brain Tumors in Adults: Diagnosis and Treatment Am. Fam. Physician 2016 93 211 217 26926614
- [17]McNeill K.A. Epidemiology of Brain Tumors Neurol. Clin. 2016 34 981 998 10.1016/j.ncl.2016.06.014 27720005 · DOI
- [18]Achrol A.S. Rennert R.C. Anders C. Soffietti R. Ahluwalia M.S. Nayak L. Peters S. Arvold N.D. Harsh G.R. Steeg P.S. Brain Metastases Nat. Rev. Dis. Primers 2019 5 5 10.1038/s41572-018-0055-y 30655533 · DOI
- [19]Gaspar L.E. Brain Metastases in Lung Cancer Expert Rev. Anticancer Ther. 2004 4 259 270 10.1586/14737140.4.2.259 15056056 · DOI
- [20]Wu A. Wei J. Kong L.-Y. Wang Y. Priebe W. Qiao W. Sawaya R. Heimberger A.B. Glioma Cancer Stem Cells Induce Immunosuppressive Macrophages/Microglia Neuro Oncol. 2010 12 1113 1125 10.1093/neuonc/noq082 20667896 PMC3098021 · DOI
- [22]Broekman M.L. Maas S.L.N. Abels E.R. Mempel T.R. Krichevsky A.M. Breakefield X.O. Multidimensional Communication in the Microenvirons of Glioblastoma Nat. Rev. Neurol. 2018 14 482 495 10.1038/s41582-018-0025-8 29985475 PMC6425928 · DOI
- [23]Palmieri D. Smith Q.R. Lockman P.R. Bronder J. Gril B. Chambers A.F. Weil R.J. Steeg P.S. Brain Metastases of Breast Cancer Breast Dis. 2007 26 139 147 10.3233/BD-2007-26112 17473372 · DOI
- [24]Michl M. Thurmaier J. Schubert-Fritschle G. Wiedemann M. Laubender R.P. Nüssler N.C. Ruppert R. Kleeff J. Schepp W. Reuter C. Brain Metastasis in Colorectal Cancer Patients: Survival and Analysis of Prognostic Factors Clin. Color. Cancer 2015 14 281 290 10.1016/j.clcc.2015.05.009 26123495 · DOI
- [25]Malmer B. Iselius L. Holmberg E. Collins A. Henriksson R. Grönberg H. Genetic Epidemiology of Glioma Br. J. Cancer 2001 84 429 434 10.1054/bjoc.2000.1612 11161412 PMC2363745 · DOI
- [26]Walker L. Thompson D. Easton D. Ponder B. Ponder M. Frayling I. Baralle D. A Prospective Study of Neurofibromatosis Type 1 Cancer Incidence in the UK Br. J. Cancer 2006 95 233 238 10.1038/sj.bjc.6603227 16786042 PMC2360616 · DOI
- [27]Taylor A.J. Little M.P. Winter D.L. Sugden E. Ellison D.W. Stiller C.A. Stovall M. Frobisher C. Lancashire E.R. Reulen R.C. Population-Based Risks of CNS Tumors in Survivors of Childhood Cancer: The British Childhood Cancer Survivor Study J. Clin. Oncol. 2010 28 5287 5293 10.1200/JCO.2009.27.0090 21079138 PMC4809645 · DOI
- [28]Shore R.E. Moseson M. Harley N. Pasternack B.S. Tumors and Other Diseases Following Childhood X-Ray Treatment for Ringworm of The Scalp (Tinea capitis) Health Phys. 2003 85 404 10.1097/00004032-200310000-00003 13678280 · DOI
- [29]Neglia J.P. Robison L.L. Stovall M. Liu Y. Packer R.J. Hammond S. Yasui Y. Kasper C.E. Mertens A.C. Donaldson S.S. New Primary Neoplasms of the Central Nervous System in Survivors of Childhood Cancer: A Report from the Childhood Cancer Survivor Study JNCI J. Natl. Cancer Inst. 2006 98 1528 1537 10.1093/jnci/djj411 17077355 · DOI
- [30]Coble J.B. Dosemeci M. Stewart P.A. Blair A. Bowman J. Fine H.A. Shapiro W.R. Selker R.G. Loeffler J.S. Black P.M. Occupational Exposure to Magnetic Fields and the Risk of Brain Tumors Neuro Oncol. 2009 11 242 249 10.1215/15228517-2009-002 19234232 PMC2718968 · DOI
- [31]Morgan L.L. Miller A.B. Sasco A. Davis D.L. Mobile Phone Radiation Causes Brain Tumors and Should Be Classified as a Probable Human Carcinogen (2A) (Review) Int. J. Oncol. 2015 46 1865 1871 10.3892/ijo.2015.2908 25738972 · DOI
- [32]Baan R. Grosse Y. Lauby-Secretan B. Ghissassi F.E. Bouvard V. Benbrahim-Tallaa L. Guha N. Islami F. Galichet L. Straif K. Carcinogenicity of Radiofrequency Electromagnetic Fields Lancet Oncol. 2011 12 624 626 Correction in Lancet Oncol. 2011, 12, 625 10.1016/S1470-2045(11)70147-4 21845765 · DOI
- [33]Schoemaker M.J. Swerdlow A.J. Hepworth S.J. McKinney P.A. van Tongeren M. Muir K.R. History of Allergies and Risk of Glioma in Adults Int. J. Cancer 2006 119 2165 2172 10.1002/ijc.22091 16823851 · DOI
- [34]Schwartzbaum J. Jonsson F. Ahlbom A. Preston-Martin S. Lönn S. Söderberg K.C. Feychting M. Cohort Studies of Association between Self-Reported Allergic Conditions, Immune-Related Diagnoses and Glioma and Meningioma Risk Int. J. Cancer 2003 106 423 428 10.1002/ijc.11230 12845684 · DOI
- [35]Schlehofer B. Blettner M. Preston-Martin S. Niehoff D. Wahrendorf J. Arslan A. Ahlbom A. Choi W.N. Giles G.G. Howe G.R. Role of Medical History in Brain Tumour Development. Results from the International Adult Brain Tumour Study Int. J. Cancer 1999 82 155 160 10.1002/(SICI)1097-0215(19990719)82:2<155::AID-IJC1>3.0.CO;2-P 10389745 · DOI
- [36]Reardon D.A. Wen P.Y. Unravelling Tumour Heterogeneity—Implications for Therapy Nat. Rev. Clin. Oncol. 2015 12 69 70 10.1038/nrclinonc.2014.223 25560529 · DOI
- [37]Jacobs A.H. Kracht L.W. Gossmann A. Rüger M.A. Thomas A.V. Thiel A. Herholz K. Imaging in Neurooncology Neurotherapeutics 2005 2 333 347 10.1602/neurorx.2.2.333 PMC1064995 15897954 · DOI
- [38]Mabray M.C. Barajas R.F. Cha S. Modern Brain Tumor Imaging Brain Tumor Res. Treat. 2015 3 8 23 10.14791/btrt.2015.3.1.8 25977902 PMC4426283 · DOI
- [40]Bangiyev L. Rossi Espagnet M.C. Young R. Shepherd T. Knopp E. Friedman K. Boada F. Fatterpekar G.M. Adult Brain Tumor Imaging: State of the Art Semin. Roentgenol. 2014 49 39 52 10.1053/j.ro.2013.11.001 24342674 · DOI
- [41]Brindle K.M. Izquierdo-García J.L. Lewis D.Y. Mair R.J. Wright A.J. Brain Tumor Imaging J. Clin. Oncol. 2017 35 2432 2438 10.1200/JCO.2017.72.7636 28640699 · DOI
- [42]van Dijken B.R.J. van Laar P.J. Holtman G.A. van der Hoorn A. Diagnostic Accuracy of Magnetic Resonance Imaging Techniques for Treatment Response Evaluation in Patients with High-Grade Glioma, a Systematic Review and Meta-Analysis Eur. Radiol. 2017 27 4129 4144 10.1007/s00330-017-4789-9 28332014 PMC5579204 · DOI
- [43]Santiago-Dieppa D.R. Steinberg J. Gonda D. Cheung V.J. Carter B.S. Chen C.C. Extracellular Vesicles as a Platform for ‘Liquid Biopsy’ in Glioblastoma Patients Expert Rev. Mol. Diagn. 2014 14 819 825 10.1586/14737159.2014.943193 25136839 PMC4436244 · DOI
- [44]Klekner Á. Szivos L. Virga J. Árkosy P. Bognár L. Birkó Z. Nagy B. Significance of Liquid Biopsy in Glioblastoma—A Review J. Biotechnol. 2019 298 82 87 10.1016/j.jbiotec.2019.04.011 30986516 · DOI
- [45]Del Bene M. Osti D. Faletti S. Beznoussenko G.V. DiMeco F. Pelicci G. Extracellular Vesicles: The Key for Precision Medicine in Glioblastoma Neuro Oncol. 2021 24 184 196 10.1093/neuonc/noab229 34581817 PMC8804888 · DOI
- [46]Global, Regional, and National Burden of Brain and Other CNS Cancer, 1990–2016: A Systematic Analysis for the Global Burden of Disease Study 2016 Lancet Neurol. 2019 18 376 393 10.1016/S1474-4422(18)30468-X 30797715 PMC6416167 · DOI
- [47]Mansoori B. Mohammadi A. Davudian S. Shirjang S. Baradaran B. The Different Mechanisms of Cancer Drug Resistance: A Brief Review Adv. Pharm. Bull. 2017 7 339 348 10.15171/apb.2017.041 29071215 PMC5651054 · DOI
- [48]Malhotra S. Miras M.C.M. Pappolla A. Montalban X. Comabella M. Liquid Biopsy in Neurological Diseases Cells 2023 12 1911 10.3390/cells12141911 37508574 PMC10378132 · DOI
- [49]Welsh J.A. Goberdhan D.C.I. O’Driscoll L. Buzas E.I. Blenkiron C. Bussolati B. Cai H. Di Vizio D. Driedonks T.A.P. Erdbrügger U. Minimal Information for Studies of Extracellular Vesicles (MISEV2023): From Basic to Advanced Approaches J. Extracell. Vesicles 2024 13 e12404 Correction in J. Extracell. Vesicles 2024, 13, e12451 10.1002/jev2.12404 38326288 PMC10850029 · DOI · Paper page
- [50]Pan B.-T. Johnstone R.M. Fate of the Transferrin Receptor during Maturation of Sheep Reticulocytes in Vitro: Selective Externalization of the Receptor Cell 1983 33 967 978 10.1016/0092-8674(83)90040-5 6307529 · DOI
- [51]Vlassov A.V. Magdaleno S. Setterquist R. Conrad R. Exosomes: Current Knowledge of Their Composition, Biological Functions, and Diagnostic and Therapeutic Potentials Biochim. Et Biophys. Acta (BBA)—General. Subj. 2012 1820 940 948 10.1016/j.bbagen.2012.03.017 22503788 · DOI
- [52]Zaborowski M.P. Balaj L. Breakefield X.O. Lai C.P. Extracellular Vesicles: Composition, Biological Relevance, and Methods of Study | BioScience | Oxford Academic BioScience 2015 65 783 797 10.1093/biosci/biv084 26955082 PMC4776721 · DOI
- [53]Doyle L.M. Wang M.Z. Overview of Extracellular Vesicles, Their Origin, Composition, Purpose, and Methods for Exosome Isolation and Analysis Cells 2019 8 727 10.3390/cells8070727 31311206 PMC6678302 · DOI
- [54]Yáñez-Mó M. Siljander P.R.-M. Andreu Z. Bedina Zavec A. Borràs F.E. Buzas E.I. Buzas K. Casal E. Cappello F. Carvalho J. Biological Properties of Extracellular Vesicles and Their Physiological Functions J. Extracell. Vesicles 2015 4 27066 10.3402/jev.v4.27066 25979354 PMC4433489 · DOI · Paper page
- [55]Tricarico C. Clancy J. D’Souza-Schorey C. Biology and Biogenesis of Shed Microvesicles Small GTPases 2016 8 220 232 10.1080/21541248.2016.1215283 27494381 PMC5680703 · DOI
- [56]Ma L. Li Y. Peng J. Wu D. Zhao X. Cui Y. Chen L. Yan X. Du Y. Yu L. Discovery of the Migrasome, an Organelle Mediating Release of Cytoplasmic Contents during Cell Migration | Cell Research Cell Res. 2014 25 24 38 10.1038/cr.2014.135 25342562 PMC4650581 · DOI
- [57]Lötvall J. Hill A.F. Hochberg F. Buzás E.I. Di Vizio D. Gardiner C. Gho Y.S. Kurochkin I.V. Mathivanan S. Quesenberry P. Minimal Experimental Requirements for Definition of Extracellular Vesicles and Their Functions: A Position Statement from the International Society for Extracellular Vesicles J. Extracell. Vesicles 2014 3 26913 10.3402/jev.v3.26913 25536934 PMC4275645 · DOI
- [58]Melentijevic I. Toth M.L. Arnold M.L. Guasp R.J. Harinath G. Nguyen K.C. Taub D. Parker J.A. Neri C. Gabel C. C. Elegans Neurons Jettison Protein Aggregates and Mitochondria Under Neurotoxic Stress Nature 2017 542 367 371 10.1038/nature21362 28178240 PMC5336134 · DOI · Paper page
- [59]Keller S. König A.-K. Marmé F. Runz S. Wolterink S. Koensgen D. Mustea A. Sehouli J. Altevogt P. Systemic Presence and Tumor-Growth Promoting Effect of Ovarian Carcinoma Released Exosomes Cancer Lett. 2009 278 73 81 10.1016/j.canlet.2008.12.028 19188015 · DOI
- [60]Alvarez S. Suazo C. Boltansky A. Ursu M. Carvajal D. Innocenti G. Vukusich A. Hurtado M. Villanueva S. Carreño J.E. Urinary Exosomes as a Source of Kidney Dysfunction Biomarker in Renal Transplantation Transplant. Proc. 2013 45 3719 3723 10.1016/j.transproceed.2013.08.079 24315007 · DOI
- [61]Sharma S. Gillespie B.M. Palanisamy V. Gimzewski J.K. Quantitative Nano-Structural and Single Molecule Force Spectroscopy Bio-Molecular Analysis of Human Saliva Derived Exosomes Langmuir 2011 27 14394 14400 10.1021/la2038763 22017459 PMC3235036 · DOI
- [62]Näslund T.I. Paquin-Proulx D. Paredes P.T. Vallhov H. Sandberg J.K. Gabrielsson S. Exosomes from Breast Milk Inhibit HIV-1 Infection of Dendritic Cells and Subsequent Viral Transfer to CD4+ T Cells AIDS 2014 28 171 10.1097/QAD.0000000000000159 24413309 · DOI
- [63]Gardiner C. Di Vizio D. Sahoo S. Théry C. Witwer K.W. Wauben M. Hill A.F. Techniques Used for the Isolation and Characterization of Extracellular Vesicles: Results of a Worldwide Survey J. Extracell. Vesicles 2016 5 32945 10.3402/jev.v5.32945 27802845 PMC5090131 · DOI
- [64]Witwer K.W. Buzás E.I. Bemis L.T. Bora A. Lässer C. Lötvall J. Nolte-‘t Hoen E.N. Piper M.G. Sivaraman S. Skog J. Standardization of Sample Collection, Isolation and Analysis Methods in Extracellular Vesicle Research J. Extracell. Vesicles 2013 2 20360 10.3402/jev.v2i0.20360 24009894 PMC3760646 · DOI
- [65]Chang W.-H. Cerione R.A. Antonyak M.A. Extracellular Vesicles and Their Roles in Cancer Progression Methods Mol. Biol. 2021 2174 143 170 10.1007/978-1-0716-0759-6_10 32813249 PMC8008708 · DOI
- [66]Dai J. Su Y. Zhong S. Cong L. Liu B. Yang J. Tao Y. He Z. Chen C. Jiang Y. Exosomes: Key Players in Cancer and Potential Therapeutic Strategy Signal Transduct. Target. Ther. 2020 5 145 10.1038/s41392-020-00261-0 32759948 PMC7406508 · DOI · Paper page
- [67]Théry C. Zitvogel L. Amigorena S. Exosomes: Composition, Biogenesis and Function Nat. Rev. Immunol. 2002 2 569 579 10.1038/nri855 12154376 · DOI
- [68]Valadi H. Ekström K. Bossios A. Sjöstrand M. Lee J.J. Lötvall J.O. Exosome-Mediated Transfer of mRNAs and microRNAs Is a Novel Mechanism of Genetic Exchange between Cells Nat. Cell Biol. 2007 9 654 659 10.1038/ncb1596 17486113 · DOI · Paper page
- [69]Caruso Bavisotto C. Scalia F. Marino Gammazza A. Carlisi D. Bucchieri F. Conway de Macario E. Macario A.J.L. Cappello F. Campanella C. Extracellular Vesicle-Mediated Cell–Cell Communication in the Nervous System: Focus on Neurological Diseases Int. J. Mol. Sci. 2019 20 434 10.3390/ijms20020434 30669512 PMC6359416 · DOI
- [70]Balaj L. Lessard R. Dai L. Cho Y.-J. Pomeroy S.L. Breakefield X.O. Skog J. Tumour Microvesicles Contain Retrotransposon Elements and Amplified Oncogene Sequences Nat. Commun. 2011 2 180 10.1038/ncomms1180 21285958 PMC3040683 · DOI
- [71]Tkach M. Théry C. Communication by Extracellular Vesicles: Where We Are and Where We Need to Go Cell 2016 164 1226 1232 10.1016/j.cell.2016.01.043 26967288 · DOI · Paper page
- [72]Jin Y. Chen K. Wang Z. Wang Y. Liu J. Lin L. Shao Y. Gao L. Yin H. Cui C. DNA in Serum Extracellular Vesicles Is Stable under Different Storage Conditions BMC Cancer 2016 16 753 10.1186/s12885-016-2783-2 27662833 PMC5035490 · DOI
- [73]Sohal I.S. Kasinski A.L. Emerging Diversity in Extracellular Vesicles and Their Roles in Cancer Front. Oncol. 2023 13 1167717 10.3389/fonc.2023.1167717 37397375 PMC10312242 · DOI
- [74]Matarredona E.R. Pastor A.M. Extracellular Vesicle-Mediated Communication between the Glioblastoma and Its Microenvironment Cells 2019 9 96 10.3390/cells9010096 31906023 PMC7017035 · DOI
- [75]Ciccocioppo F. Lanuti P. Marchisio M. Miscia S. Extracellular Vesicles Involvement in the Modulation of the Glioblastoma Environment J. Oncol. 2020 2020 3961735 10.1155/2020/3961735 32411235 PMC7204270 · DOI
- [76]Bronisz A. Godlewski J. Chiocca E.A. Extracellular Vesicles and MicroRNAs: Their Role in Tumorigenicity and Therapy for Brain Tumors Cell Mol. Neurobiol. 2016 36 361 376 10.1007/s10571-015-0293-4 26983830 PMC5570546 · DOI
- [77]Graner M.W. Alzate O. Dechkovskaia A.M. Keene J.D. Sampson J.H. Mitchell D.A. Bigner D.D. Proteomic and Immunologic Analyses of Brain Tumor Exosomes FASEB J. 2009 23 1541 1557 10.1096/fj.08-122184 19109410 PMC2669426 · DOI
- [78]Epple L.M. Griffiths S.G. Dechkovskaia A.M. Dusto N.L. White J. Ouellette R.J. Anchordoquy T.J. Bemis L.T. Graner M.W. Medulloblastoma Exosome Proteomics Yield Functional Roles for Extracellular Vesicles PLoS ONE 2012 7 e42064 10.1371/journal.pone.0042064 22848702 PMC3407172 · DOI
- [79]Nomura N. Nomura M. Sugiyama K. Hamada J.-I. Phorbol 12-Myristate 13-Acetate (PMA)-Induced Migration of Glioblastoma Cells Is Mediated via p38MAPK/Hsp27 Pathway Biochem. Pharmacol. 2007 74 690 701 10.1016/j.bcp.2007.06.018 17640620 · DOI
- [80]Khalid H. Tsutsumi K. Yamashita H. Kishikawa M. Yasunaga A. Shibata S. Expression of the Small Heat Shock Protein (Hsp) 27 in Human Astrocytomas Correlates with Histologic Grades and Tumor Growth Fractions Cell Mol. Neurobiol. 1995 15 257 268 10.1007/BF02073332 8590455 PMC11563107 · DOI
- [81]Wu Z.B. Cai L. Lin S.J. Leng Z.G. Guo Y.H. Yang W.L. Chu Y.W. Yang S. Zhao W.G. Heat Shock Protein 47 Promotes Glioma Angiogenesis Brain Pathol. 2015 26 31 42 10.1111/bpa.12256 25758142 PMC8029092 · DOI
- [82]Zhao D. Jiang X. Yao C. Zhang L. Liu H. Xia H. Wang Y. Heat Shock Protein 47 Regulated by miR-29a to Enhance Glioma Tumor Growth and Invasion J. Neuro Oncol. 2014 118 39 47 10.1007/s11060-014-1412-7 24595468 · DOI
- [83]Li G. Xu Y. Guan D. Liu Z. Liu D.X. HSP70 Protein Promotes Survival of C6 and U87 Glioma Cells by Inhibition of ATF5 Degradation J. Biol. Chem. 2011 286 20251 20259 10.1074/jbc.M110.211771 21521685 PMC3121475 · DOI
- [84]Sun G. Cao Y. Xu Y. Huai D. Chen P. Guo J. Li M. Dai Y. Overexpression of Hsc70 Promotes Proliferation, Migration, and Invasion of Human Glioma Cells J. Cell. Biochem. 2019 120 10707 10714 10.1002/jcb.28362 30816582 · DOI
- [85]Thuringer D. Hammann A. Benikhlef N. Fourmaux E. Bouchot A. Wettstein G. Solary E. Garrido C. Transactivation of the Epidermal Growth Factor Receptor by Heat Shock Protein 90 via Toll-like Receptor 4 Contributes to the Migration of Glioblastoma Cells J. Biol. Chem. 2011 286 3418 3428 10.1074/jbc.M110.154823 21127066 PMC3030348 · DOI
- [86]Memmel S. Sisario D. Zöller C. Fiedler V. Katzer A. Heiden R. Becker N. Eing L. Ferreira F.L.R. Zimmermann H. Migration Pattern, Actin Cytoskeleton Organization and Response to PI3K-, mTOR-, and Hsp90-Inhibition of Glioblastoma Cells with Different Invasive Capacities Oncotarget 2017 8 45298 45310 10.18632/oncotarget.16847 28424411 PMC5542187 · DOI
- [87]Nowosad A. Marine J.-C. Karras P. Perivascular Niches: Critical Hubs in Cancer Evolution Trends Cancer 2023 9 897 910 10.1016/j.trecan.2023.06.010 37453870 · DOI
- [88]Lucero R. Zappulli V. Sammarco A. Murillo O.D. Cheah P.S. Srinivasan S. Tai E. Ting D.T. Wei Z. Roth M.E. Glioma-Derived miRNA-Containing Extracellular Vesicles Induce Angiogenesis by Reprogramming Brain Endothelial Cells Cell Rep. 2020 30 2065 2074.e4 10.1016/j.celrep.2020.01.073 32075753 PMC7148092 · DOI
- [89]Kucharzewska P. Christianson H.C. Welch J.E. Svensson K.J. Fredlund E. Ringnér M. Mörgelin M. Bourseau-Guilmain E. Bengzon J. Belting M. Exosomes Reflect the Hypoxic Status of Glioma Cells and Mediate Hypoxia-Dependent Activation of Vascular Cells during Tumor Development Proc. Natl. Acad. Sci. USA 2013 110 7312 7317 10.1073/pnas.1220998110 23589885 PMC3645587 · DOI · Paper page
- [90]Maas S.L.N. Abels E.R. Van De Haar L.L. Zhang X. Morsett L. Sil S. Guedes J. Sen P. Prabhakar S. Hickman S.E. Glioblastoma Hijacks Microglial Gene Expression to Support Tumor Growth J. Neuroinflammation 2020 17 120 10.1186/s12974-020-01797-2 32299465 PMC7164149 · DOI
- [91]van der Vos K.E. Abels E.R. Zhang X. Lai C. Carrizosa E. Oakley D. Prabhakar S. Mardini O. Crommentuijn M.H.W. Skog J. Directly Visualized Glioblastoma-Derived Extracellular Vesicles Transfer RNA to Microglia/Macrophages in the Brain Neuro Oncol. 2016 18 58 69 10.1093/neuonc/nov244 26433199 PMC4677420 · DOI · Paper page
- [92]Peng J. Liang Q. Xu Z. Cai Y. Peng B. Li J. Zhang W. Kang F. Hong Q. Yan Y. Current Understanding of Exosomal MicroRNAs in Glioma Immune Regulation and Therapeutic Responses Front. Immunol. 2022 12 813747 10.3389/fimmu.2021.813747 35095909 PMC8796999 · DOI
- [93]Guo X. Qiu W. Liu Q. Qian M. Wang S. Zhang Z. Gao X. Chen Z. Xue H. Li G. Immunosuppressive Effects of Hypoxia-Induced Glioma Exosomes through Myeloid-Derived Suppressor Cells via the miR-10a/Rora and miR-21/Pten Pathways Oncogene 2018 37 4239 4259 10.1038/s41388-018-0261-9 29713056 · DOI
- [94]Guo X. Qiu W. Wang J. Liu Q. Qian M. Wang S. Zhang Z. Gao X. Chen Z. Guo Q. Glioma Exosomes Mediate the Expansion and Function of Myeloid-Derived Suppressor Cells through microRNA-29a/Hbp1 and microRNA-92a/Prkar1a Pathways Int. J. Cancer 2019 144 3111 3126 10.1002/ijc.32052 30536597 · DOI
- [95]Qiu W. Guo X. Li B. Wang J. Qi Y. Chen Z. Zhao R. Deng L. Qian M. Wang S. Exosomal miR-1246 from Glioma Patient Body Fluids Drives the Differentiation and Activation of Myeloid-Derived Suppressor Cells Mol. Ther. 2021 29 3449 10.1016/j.ymthe.2021.06.023 34217892 PMC8636176 · DOI
- [96]Serpe C. Monaco L. Relucenti M. Iovino L. Familiari P. Scavizzi F. Raspa M. Familiari G. Civiero L. D’Agnano I. Microglia-Derived Small Extracellular Vesicles Reduce Glioma Growth by Modifying Tumor Cell Metabolism and Enhancing Glutamate Clearance through miR-124 Cells 2021 10 2066 10.3390/cells10082066 34440835 PMC8393731 · DOI
- [97]Xue P. Huang S. Han X. Zhang C. Yang L. Xiao W. Fu J. Li H. Zhou Y. Exosomal miR-101-3p and miR-423-5p Inhibit Medulloblastoma Tumorigenesis through Targeting FOXP4 and EZH2 Cell Death Differ. 2022 29 82 95 Correction in Cell Death Differ. 2024, 31, 1391–1393 10.1038/s41418-021-00838-4 34294888 PMC8738741 · DOI
- [98]Jiang J. Lu J. Wang X. Sun B. Liu X. Ding Y. Gao G. Glioma Stem Cell-Derived Exosomal miR-944 Reduces Glioma Growth and Angiogenesis by Inhibiting AKT/ERK Signaling Aging 2021 13 19243 19259 10.18632/aging.203243 34233294 PMC8386563 · DOI
- [99]Redzic J.S. Ung T.H. Graner M.W. Glioblastoma Extracellular Vesicles: Reservoirs of Potential Biomarkers Pharmacogenomics Pers. Med. 2014 7 65 77 10.2147/pgpm.s39768 PMC3952682 24634586 · DOI
- [100]Lane R. Simon T. Vintu M. Solkin B. Koch B. Stewart N. Benstead-Hume G. Pearl F.M.G. Critchley G. Stebbing J. Cell-Derived Extracellular Vesicles Can Be Used as a Biomarker Reservoir for Glioblastoma Tumor Subtyping Commun. Biol. 2019 2 315 10.1038/s42003-019-0560-x 31453379 PMC6700082 · DOI
- [101]Wei Z. Batagov A.O. Schinelli S. Wang J. Wang Y. El Fatimy R. Rabinovsky R. Balaj L. Chen C.C. Hochberg F. Coding and Noncoding Landscape of Extracellular RNA Released by Human Glioma Stem Cells Nat. Commun. 2017 8 1145 10.1038/s41467-017-01196-x 29074968 PMC5658400 · DOI
- [102]Zhang B. Pan X. Cobb G.P. Anderson T.A. microRNAs as Oncogenes and Tumor Suppressors Dev. Biol. 2007 302 1 12 10.1016/j.ydbio.2006.08.028 16989803 · DOI
- [103]Svoronos A.A. Engelman D.M. Slack F.J. OncomiR or Tumor Suppressor? The Duplicity of MicroRNAs in Cancer Cancer Res. 2016 76 3666 3670 10.1158/0008-5472.CAN-16-0359 27325641 PMC4930690 · DOI
- [104]Whitehead C.A. Kaye A.H. Drummond K.J. Widodo S.S. Mantamadiotis T. Vella L.J. Stylli S.S. Extracellular Vesicles and Their Role in Glioblastoma Crit. Rev. Clin. Lab. Sci. 2020 57 227 252 10.1080/10408363.2019.1700208 31865806 · DOI
- [105]Basu B. Ghosh M.K. Extracellular Vesicles in Glioma: From Diagnosis to Therapy BioEssays 2019 41 1800245 10.1002/bies.201800245 31188499 · DOI
- [106]Hallal S. Mallawaaratchy D.M. Wei H. Ebrahimkhani S. Stringer B.W. Day B.W. Boyd A.W. Guillemin G.J. Buckland M.E. Kaufman K.L. Extracellular Vesicles Released by Glioblastoma Cells Stimulate Normal Astrocytes to Acquire a Tumor-Supportive Phenotype Via P53 and MYC Signaling Pathways Mol. Neurobiol. 2019 56 4566 4581 10.1007/s12035-018-1385-1 30353492 PMC6505517 · DOI
- [107]Nieland L. Morsett L.M. Broekman M.L.D. Breakefield X.O. Abels E.R. Extracellular Vesicle-Mediated Bilateral Communication between Glioblastoma and Astrocytes Trends Neurosci. 2021 44 215 226 10.1016/j.tins.2020.10.014 33234347 PMC7904598 · DOI
- [108]Oushy S. Hellwinkel J.E. Wang M. Nguyen G.J. Gunaydin D. Harland T.A. Anchordoquy T.J. Graner M.W. Glioblastoma Multiforme-Derived Extracellular Vesicles Drive Normal Astrocytes towards a Tumour-Enhancing Phenotype Philos. Trans. R. Soc. B Biol. Sci. 2017 373 20160477 10.1098/rstb.2016.0477 29158308 PMC5717433 · DOI
- [109]Mallawaaratchy D.M. Hallal S. Russell B. Ly L. Ebrahimkhani S. Wei H. Christopherson R.I. Buckland M.E. Kaufman K.L. Comprehensive Proteome Profiling of Glioblastoma-Derived Extracellular Vesicles Identifies Markers for More Aggressive Disease J. Neuro Oncol. 2017 131 233 244 10.1007/s11060-016-2298-3 PMC5306193 27770278 · DOI
- [110]Ricklefs F.L. Alayo Q. Krenzlin H. Mahmoud A.B. Speranza M.C. Nakashima H. Hayes J.L. Lee K. Balaj L. Passaro C. Immune Evasion Mediated by PD-L1 on Glioblastoma-Derived Extracellular Vesicles Sci. Adv. 2018 4 eaar2766 10.1126/sciadv.aar2766 29532035 PMC5842038 · DOI · Paper page
- [111]Yekula A. Yekula A. Muralidharan K. Kang K. Carter B.S. Balaj L. Extracellular Vesicles in Glioblastoma Tumor Microenvironment Front. Immunol. 2020 10 3137 10.3389/fimmu.2019.03137 32038644 PMC6990128 · DOI
- [112]Musatova O.E. Rubtsov Y.P. Effects of Glioblastoma-Derived Extracellular Vesicles on the Functions of Immune Cells Front. Cell Dev. Biol. 2023 11 1060000 10.3389/fcell.2023.1060000 36960410 PMC10028257 · DOI
- [113]Luong N. Lenz J.A. Modiano J.F. Olson J.K. Extracellular Vesicles Secreted by Tumor Cells Promote the Generation of Suppressive Monocytes Immunohorizons 2021 5 647 658 10.4049/immunohorizons.2000017 34404719 · DOI
- [114]Lunavat T.R. Nieland L. Vrijmoet A.B. Zargani-Piccardi A. Samaha Y. Breyne K. Breakefield X.O. Roles of Extracellular Vesicles in Glioblastoma: Foes, Friends and Informers Front. Oncol. 2023 13 1291177 10.3389/fonc.2023.1291177 38074665 PMC10704464 · DOI
- [115]Vergani E. Daveri E. Vallacchi V. Bergamaschi L. Lalli L. Castelli C. Rodolfo M. Rivoltini L. Huber V. Extracellular Vesicles in Anti-Tumor Immunity Semin. Cancer Biol. 2022 86 64 79 10.1016/j.semcancer.2021.09.004 34509614 · DOI
- [116]Lo Cicero A. Schiera G. Proia P. Saladino P. Savettieri G. Di Liegro C.M. Di Liegro I. Oligodendroglioma Cells Shed Microvesicles Which Contain TRAIL as Well as Molecular Chaperones and Induce Cell Death in Astrocytes Int. J. Oncol. 2011 39 1353 1357 10.3892/ijo.2011.1160 21842121 · DOI
- [117]D’Agostino S. Salamone M. Di Liegro I. Vittorelli M.L. Membrane Vesicles Shed by Oligodendroglioma Cells Induce Neuronal Apoptosis Int. J. Oncol. 2006 29 1075 1085 10.3892/ijo.29.5.1075 17016637 · DOI
- [118]Farcas M. Inngjerdingen M. Natural Killer Cell–Derived Extracellular Vesicles in Cancer Therapy Scand. J. Immunol. 2020 92 e12938 10.1111/sji.12938 32697853 · DOI
- [119]Zhu L. Kalimuthu S. Oh J.M. Gangadaran P. Baek S.H. Jeong S.Y. Lee S.-W. Lee J. Ahn B.-C. Enhancement of Antitumor Potency of Extracellular Vesicles Derived from Natural Killer Cells by IL-15 Priming Biomaterials 2019 190–191 38 50 10.1016/j.biomaterials.2018.10.034 30391801 · DOI
- [120]Wu C.-H. Li J. Li L. Sun J. Fabbri M. Wayne A.S. Seeger R.C. Jong A.Y. Extracellular Vesicles Derived from Natural Killer Cells Use Multiple Cytotoxic Proteins and Killing Mechanisms to Target Cancer Cells J. Extracell. Vesicles 2019 8 1588538 10.1080/20013078.2019.1588538 30891164 PMC6419691 · DOI
- [121]Raposo G. Nijman H.W. Stoorvogel W. Liejendekker R. Harding C.V. Melief C.J. Geuze H.J. B Lymphocytes Secrete Antigen-Presenting Vesicles J. Exp. Med. 1996 183 1161 1172 10.1084/jem.183.3.1161 8642258 PMC2192324 · DOI · Paper page
- [122]Wolfers J. Lozier A. Raposo G. Regnault A. Théry C. Masurier C. Flament C. Pouzieux S. Faure F. Tursz T. Tumor-Derived Exosomes Are a Source of Shared Tumor Rejection Antigens for CTL Cross-Priming Nat. Med. 2001 7 297 303 10.1038/85438 11231627 · DOI
- [123]Vengoji R. Macha M.A. Nimmakayala R.K. Rachagani S. Siddiqui J.A. Mallya K. Gorantla S. Jain M. Ponnusamy M.P. Batra S.K. Afatinib and Temozolomide Combination Inhibits Tumorigenesis by Targeting EGFRvIII-cMet Signaling in Glioblastoma Cells J. Exp. Clin. Cancer Res. 2019 38 266 10.1186/s13046-019-1264-2 31215502 PMC6582495 · DOI
- [124]Herrmann I.K. Wood M.J.A. Fuhrmann G. Extracellular Vesicles as a Next-Generation Drug Delivery Platform Nat. Nanotechnol. 2021 16 748 759 10.1038/s41565-021-00931-2 34211166 · DOI
- [125]Wolf M. Poupardin R.W. Ebner-Peking P. Andrade A.C. Blöchl C. Obermayer A. Gomes F.G. Vari B. Maeding N. Eminger E. A Functional Corona around Extracellular Vesicles Enhances Angiogenesis, Skin Regeneration and Immunomodulation J. Extracell. Vesicles 2022 11 e12207 10.1002/jev2.12207 35398993 PMC8994701 · DOI
- [126]Stamatovic S.M. Keep R.F. Andjelkovic A.V. Brain Endothelial Cell-Cell Junctions: How to “Open” the Blood Brain Barrier Curr. Neuropharmacol. 2008 6 179 192 10.2174/157015908785777210 19506719 PMC2687937 · DOI
- [127]De Vries H.E. Kuiper J. de Boer A.G. Berkel T.J.C.V. Breimer D.D. The Blood-Brain Barrier in Neuroinflammatory Diseases Pharmacol. Rev. 1997 49 143 156 10.1016/S0031-6997(24)01320-6 9228664 · DOI
- [128]Plate K.H. Scholz A. Dumont D.J. Tumor Angiogenesis and Anti-Angiogenic Therapy in Malignant Gliomas Revisited Acta Neuropathol. 2012 124 763 775 10.1007/s00401-012-1066-5 23143192 PMC3508273 · DOI
- [129]Papadopoulos M.C. Saadoun S. Woodrow C.J. Davies D.C. Costa-Martins P. Moss R.F. Krishna S. Bell B.A. Occludin Expression in Microvessels of Neoplastic and Non-Neoplastic Human Brain Neuropathol. Appl. Neurobiol. 2001 27 384 395 10.1046/j.0305-1846.2001.00341.x 11679090 · DOI
- [130]Liebner S. Fischmann A. Rascher G. Duffner F. Grote E.-H. Kalbacher H. Wolburg H. Claudin-1 and Claudin-5 Expression and Tight Junction Morphology Are Altered in Blood Vessels of Human Glioblastoma Multiforme Acta Neuropathol. 2000 100 323 331 10.1007/s004010000180 10965803 · DOI
- [131]Wolburg H. Wolburg-Buchholz K. Kraus J. Rascher-Eggstein G. Liebner S. Hamm S. Duffner F. Grote E.-H. Risau W. Engelhardt B. Localization of Claudin-3 in Tight Junctions of the Blood-Brain Barrier Is Selectively Lost during Experimental Autoimmune Encephalomyelitis and Human Glioblastoma Multiforme Acta Neuropathol. 2003 105 586 592 10.1007/s00401-003-0688-z 12734665 · DOI
- [132]de Vries H.E. Blom-Roosemalen M.C.M. van Oosten M. de Boer A.G. van Berkel T.J.C. Breimer D.D. Kuiper J. The Influence of Cytokines on the Integrity of the Blood-Brain Barrier In Vitro J. Neuroimmunol. 1996 64 37 43 10.1016/0165-5728(95)00148-4 8598388 · DOI
- [133]Jiang X.-C. Gao J.-Q. Exosomes as Novel Bio-Carriers for Gene and Drug Delivery Int. J. Pharm. 2017 521 167 175 10.1016/j.ijpharm.2017.02.038 28216464 · DOI
- [134]Sun D. Zhuang X. Xiang X. Liu Y. Zhang S. Liu C. Barnes S. Grizzle W. Miller D. Zhang H.-G. A Novel Nanoparticle Drug Delivery System: The Anti-Inflammatory Activity of Curcumin Is Enhanced When Encapsulated in Exosomes Mol. Ther. 2010 18 1606 1614 10.1038/mt.2010.105 20571541 PMC2956928 · DOI
- [135]Han Y. Jones T.W. Dutta S. Zhu Y. Wang X. Narayanan S.P. Fagan S.C. Zhang D. Han Y. Jones T.W. Overview and Update on Methods for Cargo Loading into Extracellular Vesicles Processes 2021 9 356 10.3390/pr9020356 33954091 PMC8096148 · DOI
- [136]Antimisiaris S.G. Mourtas S. Marazioti A. Exosomes and Exosome-Inspired Vesicles for Targeted Drug Delivery Pharmaceutics 2018 10 218 10.3390/pharmaceutics10040218 30404188 PMC6321407 · DOI
- [137]Wang L. Yu X. Zhou J. Su C. Extracellular Vesicles for Drug Delivery in Cancer Treatment Biol. Proced. Online 2023 25 28 10.1186/s12575-023-00220-3 37946166 PMC10634104 · DOI
- [139]Liu X. Cao Z. Wang W. Zou C. Wang Y. Pan L. Jia B. Zhang K. Zhang W. Li W. Engineered Extracellular Vesicle-Delivered CRISPR/Cas9 for Radiotherapy Sensitization of Glioblastoma ACS Nano 2023 17 16432 16447 10.1021/acsnano.2c12857 37646615 PMC10510715 · DOI · Paper page
- [140]Zhan Y. Song Y. Qiao W. Sun L. Wang X. Yi B. Yang X. Ji L. Su P. Zhao W. Focused Ultrasound Combined with miR-1208-Equipped Exosomes Inhibits Malignant Progression of Glioma Br. J. Cancer 2023 129 1083 1094 10.1038/s41416-023-02393-w 37580442 PMC10539517 · DOI
- [141]Zhou X. Huang Q. Jiang Y. Tang H. Zhang L. Li D. Xu Y. Emerging Technologies for Engineering of Extracellular Vesicles Front. Bioeng. Biotechnol. 2023 11 1298746 10.3389/fbioe.2023.1298746 38026881 PMC10666158 · DOI
- [142]Rhim W.-K. Kim J.Y. Lee S.Y. Cha S.-G. Park J.M. Park H.J. Park C.G. Han D.K. Recent Advances in Extracellular Vesicle Engineering and Its Applications to Regenerative Medicine Biomater. Res. 2023 27 130 10.1186/s40824-023-00468-6 38082304 PMC10712135 · DOI
- [143]Smyth T. Kullberg M. Malik N. Smith-Jones P. Graner M.W. Anchordoquy T.J. Biodistribution and Delivery Efficiency of Unmodified Tumor-Derived Exosomes J. Control. Release 2015 199 145 155 10.1016/j.jconrel.2014.12.013 25523519 PMC4441346 · DOI
- [144]Gresch O. Engel F.B. Nesic D. Tran T.T. England H.M. Hickman E.S. Körner I. Gan L. Chen S. Castro-Obregon S. New Non-Viral Method for Gene Transfer into Primary Cells Methods 2004 33 151 163 10.1016/j.ymeth.2003.11.009 15121170 · DOI
- [145]Oliveira F.D. Castanho M.A.R.B. Neves V. Exosomes and Brain Metastases: A Review on Their Role and Potential Applications Int. J. Mol. Sci. 2021 22 10899 10.3390/ijms221910899 34639239 PMC8509735 · DOI
- [146]Fuhrmann G. Serio A. Mazo M. Nair R. Stevens M.M. Active Loading into Extracellular Vesicles Significantly Improves the Cellular Uptake and Photodynamic Effect of Porphyrins J. Control. Release 2015 205 35 44 10.1016/j.jconrel.2014.11.029 25483424 · DOI
- [147]Zhang D. Lee H. Zhu Z. Minhas J.K. Jin Y. Enrichment of Selective miRNAs in Exosomes and Delivery of Exosomal miRNAs in Vitro and in Vivo Am. J. Physiol.-Lung Cell. Mol. Physiol. 2017 312 L110 L121 10.1152/ajplung.00423.2016 27881406 PMC5283929 · DOI
- [148]Kamerkar S. LeBleu V.S. Sugimoto H. Yang S. Ruivo C.F. Melo S.A. Lee J.J. Kalluri R. Exosomes Facilitate Therapeutic Targeting of Oncogenic KRAS in Pancreatic Cancer Nature 2017 546 498 503 10.1038/nature22341 28607485 PMC5538883 · DOI · Paper page
- [149]Ohno S. Takanashi M. Sudo K. Ueda S. Ishikawa A. Matsuyama N. Fujita K. Mizutani T. Ohgi T. Ochiya T. Systemically Injected Exosomes Targeted to EGFR Deliver Antitumor MicroRNA to Breast Cancer Cells Mol. Ther. 2013 21 185 191 10.1038/mt.2012.180 23032975 PMC3538304 · DOI · Paper page
- [150]Gong C. Tian J. Wang Z. Gao Y. Wu X. Ding X. Qiang L. Li G. Han Z. Yuan Y. Functional Exosome-Mediated Co-Delivery of Doxorubicin and Hydrophobically Modified microRNA 159 for Triple-Negative Breast Cancer Therapy J. Nanobiotechnology 2019 17 93 10.1186/s12951-019-0526-7 31481080 PMC6721253 · DOI
- [151]Bellavia D. Raimondo S. Calabrese G. Forte S. Cristaldi M. Patinella A. Memeo L. Manno M. Raccosta S. Diana P. Interleukin 3- Receptor Targeted Exosomes Inhibit In Vitro and In Vivo Chronic Myelogenous Leukemia Cell Growth Theranostics 2017 7 1333 1345 10.7150/thno.17092 28435469 PMC5399597 · DOI
- [152]Barnwal A. Ganguly S. Bhattacharyya J. Multifaceted Nano-DEV-IL for Sustained Release of IL-12 to Avert the Immunosuppressive Tumor Microenvironment and IL-12-Associated Toxicities ACS Appl. Mater. Interfaces 2023 15 20012 20026 10.1021/acsami.3c02934 37068138 · DOI
- [153]Tibensky M. Jakubechova J. Altanerova U. Pastorakova A. Rychly B. Baciak L. Mravec B. Altaner C. Gene-Directed Enzyme/Prodrug Therapy of Rat Brain Tumor Mediated by Human Mesenchymal Stem Cell Suicide Gene Extracellular Vesicles In Vitro and In Vivo Cancers 2022 14 735 10.3390/cancers14030735 35159002 PMC8833758 · DOI
- [154]Adamus T. Hung C.-Y. Yu C. Kang E. Hammad M. Flores L. Nechaev S. Zhang Q. Gonzaga J.M. Muthaiyah K. Glioma-Targeted Delivery of Exosome-Encapsulated Antisense Oligonucleotides Using Neural Stem Cells Mol. Ther. Nucleic Acids 2021 27 611 620 10.1016/j.omtn.2021.12.029 35036069 PMC8752899 · DOI
- [155]Xu F. Jiang D. Xu J. Dai H. Fan Q. Fei Z. Wang B. Zhang Y. Ma Q. Yang Q. Engineering of Dendritic Cell Bispecific Extracellular Vesicles for Tumor-Targeting Immunotherapy Cell Rep. 2023 42 113138 10.1016/j.celrep.2023.113138 37738123 · DOI
- [156]Hosseini N.F. Amini R. Ramezani M. Saidijam M. Hashemi S.M. Najafi R. AS1411 Aptamer-Functionalized Exosomes in the Targeted Delivery of Doxorubicin in Fighting Colorectal Cancer Biomed. Pharmacother. 2022 155 113690 10.1016/j.biopha.2022.113690 36099793 · DOI
- [157]Zhao M. Li Q. Zhao Y. Zhou H. Yan Y. Kong R.-M. Tan Q. Kong W. Qu F. Dual-Aptamer Recognition of DNA Logic Gate Sensor-Based Specific Exosomal Proteins for Ovarian Cancer Diagnosis ACS Sens. 2024 9 2540 2549 10.1021/acssensors.4c00270 38635557 · DOI
- [158]Agosti E. Antonietti S. Ius T. Fontanella M.M. Zeppieri M. Panciani P.P. Agosti E. Antonietti S. Ius T. Fontanella M.M. A Systematic Review of Mesenchymal Stem Cell-Derived Extracellular Vesicles: A Potential Treatment for Glioblastoma Brain Sci. 2024 14 1058 10.3390/brainsci14111058 39595821 PMC11591642 · DOI
- [159]Villa A. De Mitri Z. Vincenti S. Crippa E. Castiglioni L. Gelosa P. Rebecchi M. Tosi D. Brunialti E. Oevermann A. Canine Glioblastoma-Derived Extracellular Vesicles as Precise Carriers for Glioblastoma Imaging: Targeting across the Blood-Brain Barrier Biomed. Pharmacother. 2024 172 116201 10.1016/j.biopha.2024.116201 38306846 · DOI
- [160]Indira Chandran V. Gopala S. Venkat E.H. Kjolby M. Nejsum P. Extracellular Vesicles in Glioblastoma: A Challenge and an Opportunity npj Precis. Oncol. 2024 8 103 10.1038/s41698-024-00600-2 38760427 PMC11101656 · DOI
- [161]Keskin D.B. Anandappa A.J. Sun J. Tirosh I. Mathewson N.D. Li S. Oliveira G. Giobbie-Hurder A. Felt K. Gjini E. Neoantigen Vaccine Generates Intratumoral T Cell Responses in Phase Ib Glioblastoma Trial Nature 2019 565 234 239 10.1038/s41586-018-0792-9 30568305 PMC6546179 · DOI · Paper page
- [162]Ahluwalia M.S. Reardon D.A. Abad A.P. Curry W.T. Wong E.T. Figel S.A. Mechtler L.L. Peereboom D.M. Hutson A.D. Withers H.G. Phase IIa Study of SurVaxM Plus Adjuvant Temozolomide for Newly Diagnosed Glioblastoma J. Clin. Oncol. 2023 41 1453 1465 10.1200/JCO.22.00996 36521103 PMC9995096 · DOI
- [163]Adhikari A.S. Macauley J. Johnson Y. Connolly M. Coleman T. Heiland T. Development and Characterization of an HCMV Multi-Antigen Therapeutic Vaccine for Glioblastoma Using the UNITE Platform Front. Oncol. 2022 12 850546 10.3389/fonc.2022.850546 35651802 PMC9149224 · DOI
- [164]Tenchov R. Bird R. Curtze A.E. Zhou Q. Lipid Nanoparticles—From Liposomes to mRNA Vaccine Delivery, a Landscape of Research Diversity and Advancement ACS Nano 2021 15 16982 17015 10.1021/acsnano.1c04996 34181394 · DOI · Paper page
- [165]Zhao C. Zhu X. Tan J. Mei C. Cai X. Kong F. Lipid-Based Nanoparticles to Address the Limitations of GBM Therapy by Overcoming the Blood-Brain Barrier, Targeting Glioblastoma Stem Cells, and Counteracting the Immunosuppressive Tumor Microenvironment Biomed. Pharmacother. 2024 171 116113 10.1016/j.biopha.2023.116113 38181717 · DOI
- [166]Bader J. Brigger F. Leroux J.-C. Extracellular Vesicles versus Lipid Nanoparticles for the Delivery of Nucleic Acids Adv. Drug Deliv. Rev. 2024 215 115461 10.1016/j.addr.2024.115461 39490384 · DOI
- [167]Cheng K. Kalluri R. Guidelines for Clinical Translation and Commercialization of Extracellular Vesicles and Exosomes Based Therapeutics Extracell. Vesicle 2023 2 100029 10.1016/j.vesic.2023.100029 · DOI
- [168]Papait A. Perini G. Palmieri V. Cargnoni A. Vertua E. Pasotti A. Rosa E. De Spirito M. Silini A.R. Papi M. Defining the Immunological Compatibility of Graphene Oxide-Loaded PLGA Scaffolds for Biomedical Applications Biomater. Adv. 2024 165 214024 10.1016/j.bioadv.2024.214024 39232353 · DOI
- [169]Konoshenko M.Y. Lekchnov E.A. Vlassov A.V. Laktionov P.P. Isolation of Extracellular Vesicles: General Methodologies and Latest Trends BioMed Res. Int. 2018 2018 8545347 10.1155/2018/8545347 29662902 PMC5831698 · DOI
- [170]Chen J. Li P. Zhang T. Xu Z. Huang X. Wang R. Du L. Review on Strategies and Technologies for Exosome Isolation and Purification Front. Bioeng. Biotechnol. 2022 9 811971 10.3389/fbioe.2021.811971 35071216 PMC8766409 · DOI · Paper page
- [171]Stawarska A. Bamburowicz-Klimkowska M. Runden-Pran E. Dusinska M. Cimpan M.R. Rios-Mondragon I. Grudzinski I.P. Stawarska A. Bamburowicz-Klimkowska M. Runden-Pran E. Extracellular Vesicles as Next-Generation Diagnostics and Advanced Therapy Medicinal Products Int. J. Mol. Sci. 2024 25 6533 10.3390/ijms25126533 38928240 PMC11204223 · DOI
- [172]St-Denis-Bissonnette F. Cummings S.E. Qiu S. Stalker A. Muradia G. Mehic J. Mediratta K. Kaczmarek S. Burger D. Lee S.-H. A Clinically Relevant Large-Scale Biomanufacturing Workflow to Produce Natural Killer Cells and Natural Killer Cell-Derived Extracellular Vesicles for Cancer Immunotherapy J. Extracell. Vesicles 2023 12 e12387 10.1002/jev2.12387 38054534 PMC10698709 · DOI
- Authors
- Colangelo, T., Saponaro, A. A., Mazzoccoli, G., Serviddio, G., & Villani, R.
- Affiliations
- University of Foggia (IT)
- Casa Sollievo della Sofferenza (IT)
- Corresponding author
- Serviddio, Gaetano
- ORCID
- Venue
- International Journal of Molecular Sciences
- Publisher
- MDPI AG
- Published
- 2025-12-07
- Volume
- 26
- Issue
- 24
- Pages
- 11826
- ISSN
- 1422-0067 (ISSN-L)
- PMC
- PMC12733313
- OpenAlex
- W4417106642
- Cited by
- 1
- References
- 164
- Citations by year
- 2026: 1
- FWCI
- 0.09
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- International Journal of Molecular Sciences (publishedVersion, cc-by)
- PubMed (publishedVersion)
- PubMed Central (publishedVersion, cc-by)
- Funders
- European Commission
- Fondazione Umberto Veronesi
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Health Sciences › Medicine › Genetics › Glioma Diagnosis and Treatment
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Keywords
- extracellular vesicles, glioblastoma, brain tumors, liquid biopsy, microRNA, blood-brain barrier drug delivery, nanotherapeutics, tumor heterogeneity, treatment resistance, immune evasion, biomarkers
- MeSH terms
- Extracellular Vesicles, Animals, Blood-Brain Barrier, Brain Neoplasms, Glioblastoma, Humans, Biomarkers, Tumor, Drug Delivery Systems
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