Research progress of exosome biosensors
DOI:
https://doi.org/10.54097/jc9pgs54Keywords:
Exosome, Biosensor, Detection.Abstract
At present, cancer is still an important cause of high morbidity and mortality worldwide. Early diagnosis has become the key to improving the cure rate and life quality of patients. Exosomes are small extracellular vesicles that play important roles in intercellular communication. Exosomes contain a variety of biomarkers, such as DNA, RNA, proteins, lipids, and metabolites, which reflect the state of the parent cell. Since exosomes affect tumorigenesis and metastasis in cancer patients, they are excellent non-invasive potential indicators for early cancer detection. In addition, the growing understanding of the structure and function of cancer marker exosomes provides new solutions for early cancer detection. Nowadays, the main cancer screening methods (ultrasound, nuclear magnetic resonance, tissue biopsy, etc.) are expensive, time-consuming, and require professionals to operate imaging, etc. Exosome biosensors have become effective tools for early cancer diagnosis due to their advantages of simple operation and cost-effectiveness. Therefore, based on the structure and function of exosomes, this study summarizes the research progress of different types of biosensor detection, discusses the characteristics of current biosensors, and looks forward to future research trends.
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Siegel R L, Miller K D, Jemal A. Cancer statistics, 2019 [J]. CA: A Cancer Journal for Clinicians, 2019, 69(1): 7-34.
Del Ciello A, Franchi P, Contegiacomo A, et al. Missed lung cancer: When, where, and why? [J]. Diagnostic and Interventional Radiology, 2017, 23(2): 118-126.
Sharma S, Zuñiga F, Rice G E, et al. Tumor-derived exosomes in ovarian cancer - liquid biopsies for early detection and real-time monitoring of cancer progression [J]. Oncotarget, 2017, 8(61): 104687-104703.
Trams E G, Lauter C J, Salem N, Jr., et al. Exfoliation of membrane ecto-enzymes in the form of micro-vesicles [J]. Biochimica et Biophysica Acta, 1981, 645(1): 63-70.
Johnstone R M. The jeanne manery-fisher memorial lecture 1991. Maturation of reticulocytes: Formation of exosomes as a mechanism for shedding membrane proteins [J]. Biochemistry and Cell Biology, 1992, 70(3-4): 179-190.
Théry C, Witwer K W, Aikawa E, et al. Minimal information for studies of extracellular vesicles 2018 (misev2018): A position statement of the international society for extracellular vesicles and update of the misev2014 guidelines [J]. Journal of extracellular vesicles, 2018, 7(1): 1535750.
Yang X X, Sun C, Wang L, et al. New insight into isolation, identification techniques and medical applications of exosomes [J]. Journal of controlled release : official journal of the Controlled Release Society, 2019, 308: 119-129.
Jeppesen D K, Fenix A M, Franklin J L, et al. Reassessment of exosome composition [J]. Cell, 2019, 177(2): 428-445.e418.
Maecker H T, Todd S C, Levy S. The tetraspanin superfamily: Molecular facilitators [J]. FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 1997, 11(6): 428-442.
Kumari S, Devi G T, Badana A, et al. Cd151-a striking marker for cancer therapy [J]. Biomarkers in Cancer, 2015, 7: 7-11.
Boucheix C, Rubinstein E. Tetraspanins [J]. Cellular and molecular life sciences : CMLS, 2001, 58(9): 1189-1205.
Azorsa D O, Hyman J A, Hildreth J E. Cd63/pltgp40: A platelet activation antigen identical to the stage-specific, melanoma-associated antigen me491 [J]. Blood, 1991, 78(2): 280-284.
Wright M D, Tomlinson M G. The ins and outs of the transmembrane 4 superfamily [J]. Immunology Today, 1994, 15(12): 588-594.
Pols M S, Klumperman J. Trafficking and function of the tetraspanin cd63 [J]. Experimental cell research, 2009, 315(9): 1584-1592.
Peters P J, Borst J, Oorschot V, et al. Cytotoxic t lymphocyte granules are secretory lysosomes, containing both perforin and granzymes [J]. The Journal of experimental medicine, 1991, 173(5): 1099-1109.
Escola J M, Kleijmeer M J, Stoorvogel W, et al. Selective enrichment of tetraspan proteins on the internal vesicles of multivesicular endosomes and on exosomes secreted by human b-lymphocytes [J]. The Journal of biological chemistry, 1998, 273(32): 20121-20127.
Heijnen H F, Debili N, Vainchencker W, et al. Multivesicular bodies are an intermediate stage in the formation of platelet alpha-granules [J]. Blood, 1998, 91(7): 2313-2325.
Arribas M, Cutler D F. Weibel-palade body membrane proteins exhibit differential trafficking after exocytosis in endothelial cells [J]. Traffic, 2000, 1(10): 783-793.
Raposo G, Marks M S, Cutler D F. Lysosome-related organelles: Driving post-golgi compartments into specialisation [J]. Current opinion in cell biology, 2007, 19(4): 394-401.
Stoorvogel W, Kleijmeer M J, Geuze H J, et al. The biogenesis and functions of exosomes [J]. Traffic, 2002, 3(5): 321-330.
Tarrant J M, Robb L, Van Spriel A B, et al. Tetraspanins: Molecular organisers of the leukocyte surface [J]. Trends in Immunology, 2003, 24(11): 610-617.
Berditchevski F. Complexes of tetraspanins with integrins: More than meets the eye [J]. Journal of cell science, 2001, 114(Pt 23): 4143-4151.
Skubitz K M, Campbell K D, Iida J, et al. Cd63 associates with tyrosine kinase activity and cd11/cd18, and transmits an activation signal in neutrophils [J]. Journal of immunology, 1996, 157(8): 3617-3626.
Sincock P M, Mayrhofer G, Ashman L K. Localization of the transmembrane 4 superfamily (tm4sf) member peta-3 (cd151) in normal human tissues: Comparison with cd9, cd63, and alpha5beta1 integrin [J]. The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 1997, 45(4): 515-525.
Rubinstein E, Le Naour F, Lagaudrière-Gesbert C, et al. Cd9, cd63, cd81, and cd82 are components of a surface tetraspan network connected to hla-dr and vla integrins [J]. European journal of immunology, 1996, 26(11): 2657-2665.
Hirst J, Bright N A, Rous B, et al. Characterization of a fourth adaptor-related protein complex [J]. Molecular biology of the cell, 1999, 10(8): 2787-2802.
Latysheva N, Muratov G, Rajesh S, et al. Syntenin-1 is a new component of tetraspanin-enriched microdomains: Mechanisms and consequences of the interaction of syntenin-1 with cd63 [J]. Molecular and cellular biology, 2006, 26(20): 7707-7718.
Doyle E L, Ridger V, Ferraro F, et al. Cd63 is an essential cofactor to leukocyte recruitment by endothelial p-selectin [J]. Blood, 2011, 118(15): 4265-4273.
Tugues S, Honjo S, König C, et al. Tetraspanin cd63 promotes vascular endothelial growth factor receptor 2-β1 integrin complex formation, thereby regulating activation and downstream signaling in endothelial cells in vitro and in vivo [J]. The Journal of biological chemistry, 2013, 288(26): 19060-19071.
Pfistershammer K, Majdic O, Stöckl J, et al. Cd63 as an activation-linked t cell costimulatory element [J]. Journal of immunology, 2004, 173(10): 6000-6008.
Voellmy R. On mechanisms that control heat shock transcription factor activity in metazoan cells [J]. Cell Stress & Chaperones, 2004, 9(2): 122-133.
Pinhasi-Kimhi O, Michalovitz D, Ben-Zeev A, et al. Specific interaction between the p53 cellular tumour antigen and major heat shock proteins [J]. Nature, 1986, 320(6058): 182-184.
Daniels G A, Sanchez-Perez L, Diaz R M, et al. A simple method to cure established tumors by inflammatory killing of normal cells [J]. Nature Biotechnology, 2004, 22(9): 1125-1132.
Ciocca D R, Calderwood S K. Heat shock proteins in cancer: Diagnostic, prognostic, predictive, and treatment implications [J]. Cell Stress & Chaperones, 2005, 10(2): 86-103.
Calderwood S K, Gong J. Heat shock proteins promote cancer: It's a protection racket [J]. Trends in biochemical sciences, 2016, 41(4): 311-323.
Baldin A V, Zamyatnin A A, Jr., Bazhin A V, et al. Advances in the development of anticancer hsp-based vaccines [J]. Current Medicinal Chemistry, 2019, 26(3): 427-445.
Zhong Q, Chen Y, Jones D, et al. Perturbation of tsg101 protein affects cell cycle progression [J]. Cancer Research, 1998, 58(13): 2699-2702.
Zhong Q, Chen C F, Chen Y, et al. Identification of cellular tsg101 protein in multiple human breast cancer cell lines [J]. Cancer Research, 1997, 57(19): 4225-4228.
Xie W, Li L, Cohen S N. Cell cycle-dependent subcellular localization of the tsg101 protein and mitotic and nuclear abnormalities associated with tsg101 deficiency [J]. Proceedings of the National Academy of Sciences of the United States of America, 1998, 95(4): 1595-1600.
Hittelman A B, Burakov D, Iñiguez-Lluhí J A, et al. Differential regulation of glucocorticoid receptor transcriptional activation via af-1-associated proteins [J]. The EMBO Journal, 1999, 18(19): 5380-5388.
Lin Y S, Chen Y J, Cohen S N, et al. Identification of tsg101 functional domains and p21 loci required for tsg101-mediated p21 gene regulation [J]. PloS One, 2013, 8(11): e79674.
Oh H, Mammucari C, Nenci A, et al. Negative regulation of cell growth and differentiation by tsg101 through association with p21(cip1/waf1) [J]. Proceedings of the National Academy of Sciences of the United States of America, 2002, 99(8): 5430-5435.
Lee H H, Elia N, Ghirlando R, et al. Midbody targeting of the escrt machinery by a noncanonical coiled coil in cep55 [J]. Science, 2008, 322(5901): 576-580.
Katzmann D J, Babst M, Emr S D. Ubiquitin-dependent sorting into the multivesicular body pathway requires the function of a conserved endosomal protein sorting complex, escrt-i [J]. Cell, 2001, 106(2): 145-155.
Oh K B, Stanton M J, West W W, et al. Tsg101 is upregulated in a subset of invasive human breast cancers and its targeted overexpression in transgenic mice reveals weak oncogenic properties for mammary cancer initiation [J]. Oncogene, 2007, 26(40): 5950-5959.
Liu F, Yu Y, Jin Y, et al. Tsg101, identified by screening a cancer cdna library and soft agar assay, promotes cell proliferation in human lung cancer [J]. Molecular biology reports, 2010, 37(6): 2829-2838.
Liu R T, Huang C C, You H L, et al. Overexpression of tumor susceptibility gene tsg101 in human papillary thyroid carcinomas [J]. Oncogene, 2002, 21(31): 4830-4837.
Young T W, Mei F C, Rosen D G, et al. Up-regulation of tumor susceptibility gene 101 protein in ovarian carcinomas revealed by proteomics analyses [J]. Molecular & cellular proteomics : MCP, 2007, 6(2): 294-304.
Young T W, Rosen D G, Mei F C, et al. Up-regulation of tumor susceptibility gene 101 conveys poor prognosis through suppression of p21 expression in ovarian cancer [J]. Clinical cancer research : an official journal of the American Association for Cancer Research, 2007, 13(13): 3848-3854.
Ma X R, Edmund Sim U H, Pauline B, et al. Overexpression of wnt2 and tsg101 genes in colorectal carcinoma [J]. Tropical biomedicine, 2008, 25(1): 46-57.
Cheng X, Young T W, Mei F C. Proteomics analyses of ovarian cancer using genetically defined human ovarian cancer models [J]. Frontiers in bioscience : a journal and virtual library, 2007, 12: 5166-5174.
Jiang X, Wang J, Deng X, et al. Role of the tumor microenvironment in pd-l1/pd-1-mediated tumor immune escape [J]. Molecular Cancer, 2019, 18(1): 10.
Kim J M, Chen D S. Immune escape to pd-l1/pd-1 blockade: Seven steps to success (or failure) [J]. Annals of Oncology, 2016, 27(8): 1492-1504.
Saito R, Abe H, Kunita A, et al. Overexpression and gene amplification of pd-l1 in cancer cells and pd-l1(+) immune cells in epstein-barr virus-associated gastric cancer: The prognostic implications [J]. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, 2017, 30(3): 427-439.
Wang X, Teng F, Kong L, et al. Pd-l1 expression in human cancers and its association with clinical outcomes [J]. OncoTargets and Therapy, 2016, 9: 5023-5039.
Patsoukis N, Wang Q, Strauss L, et al. Revisiting the pd-1 pathway [J]. Science advances, 2020, 6(38).
Yokosuka T, Takamatsu M, Kobayashi-Imanishi W, et al. Programmed cell death 1 forms negative costimulatory microclusters that directly inhibit t cell receptor signaling by recruiting phosphatase shp2 [J]. The Journal of experimental medicine, 2012, 209(6): 1201-1217.
Marzec M, Zhang Q, Goradia A, et al. Oncogenic kinase npm/alk induces through stat3 expression of immunosuppressive protein cd274 (pd-l1, b7-h1) [J]. Proceedings of the National Academy of Sciences of the United States of America, 2008, 105(52): 20852-20857.
Akinleye A, Rasool Z. Immune checkpoint inhibitors of pd-l1 as cancer therapeutics [J]. Journal of Hematology & Oncology, 2019, 12(1): 92.
Baeuerle P A, Gires O. Epcam (cd326) finding its role in cancer [J]. British Journal of Cancer, 2007, 96(3): 417-423.
Balzar M, Winter M J, De Boer C J, et al. The biology of the 17-1a antigen (ep-cam) [J]. Journal of Molecular Medicine (Berlin, Germany), 1999, 77(10): 699-712.
Winter M J, Nagelkerken B, Mertens A E, et al. Expression of ep-cam shifts the state of cadherin-mediated adhesions from strong to weak [J]. Experimental cell research, 2003, 285(1): 50-58.
Nübel T, Preobraschenski J, Tuncay H, et al. Claudin-7 regulates epcam-mediated functions in tumor progression [J]. Molecular cancer research : MCR, 2009, 7(3): 285-299.
Maetzel D, Denzel S, Mack B, et al. Nuclear signalling by tumour-associated antigen epcam [J]. Nature cell biology, 2009, 11(2): 162-171.
Litvinov S V, Velders M P, Bakker H A, et al. Ep-cam: A human epithelial antigen is a homophilic cell-cell adhesion molecule [J]. The Journal of cell biology, 1994, 125(2): 437-446.
Basak S, Speicher D, Eck S, et al. Colorectal carcinoma invasion inhibition by co17-1a/ga733 antigen and its murine homologue [J]. Journal of the National Cancer Institute, 1998, 90(9): 691-697.
Huang Z, Zhu D, Wu L, et al. Six serum-based mirnas as potential diagnostic biomarkers for gastric cancer [J]. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2017, 26(2): 188-196.
Yuwen D, Ma Y, Wang D, et al. Prognostic role of circulating exosomal mir-425-3p for the response of nsclc to platinum-based chemotherapy [J]. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2019, 28(1): 163-173.
Han X. Study on ultrasensitive detection methods of epigenetic biomarkers DNA methylation and microrna point mutation [D]. Shandong Normal University, 2022.
Chiu S W, Tang K T. Towards a chemiresistive sensor-integrated electronic nose: A review [J]. Sensors (Basel, Switzerland), 2013, 13(10): 14214-14247.
Loutfi A, Coradeschi S, Mani G K, et al. Electronic noses for food quality: A review [J]. Journal of Food Engineering, 2015, 144: 103-111.
Kaushik A, Jayant R D, Tiwari S, et al. Nano-biosensors to detect beta-amyloid for alzheimer's disease management [J]. Biosensors and Bioelectronics, 2016, 80: 273-287.
Ibrahim N, Jamaluddin N D, Tan L L, et al. A review on the development of gold and silver nanoparticles-based biosensor as a detection strategy of emerging and pathogenic rna virus [J]. Sensors (Basel, Switzerland), 2021, 21(15).
Wu J, Lu Y, Ren N, et al. Dnazyme-functionalized r-phycoerythrin as a cost-effective and environment-friendly fluorescent biosensor for aqueous pb(2+) detection [J]. Sensors (Basel, Switzerland), 2019, 19(12).
Iwanaga M. Rapid detection of attomolar sars-cov-2 nucleic acids in all-dielectric metasurface biosensors [J]. Biosensors, 2022, 12(11).
Wang H, Wang H, Zhang M, et al. A label-free aptamer-based biosensor for microrna detection by the rna-regulated fluorescence of malachite green [J]. RSC advances, 2019, 9(56): 32906-32910.
Li S, Zhu L, Zhu L, et al. A sandwich-based evanescent wave fluorescent biosensor for simple, real-time exosome detection(†) [J]. Biosensors and Bioelectronics, 2022, 200: 113902.
Steglich P, Lecci G, Mai A. Surface plasmon resonance (spr) spectroscopy and photonic integrated circuit (pic) biosensors: A comparative review [J]. Sensors (Basel, Switzerland), 2022, 22(8).
Gaudreault J, Forest-Nault C, De Crescenzo G, et al. On the use of surface plasmon resonance-based biosensors for advanced bioprocess monitoring [J]. Processes, 2021, 9(11).
Liu C, Zeng X, An Z, et al. Sensitive detection of exosomal proteins via a compact surface plasmon resonance biosensor for cancer diagnosis [J]. ACS Sensors, 2018, 3(8): 1471-1479.
Sharma B, Frontiera R R, Henry A-I, et al. Sers: Materials, applications, and the future [J]. Materials Today, 2012, 15(1-2): 16-25.
Ju J, Hsieh C M, Tian Y, et al. Surface enhanced raman spectroscopy based biosensor with a microneedle array for minimally invasive in vivo glucose measurements [J]. ACS Sensors, 2020, 5(6): 1777-1785.
Czamara K, Adamczyk A, Stojak M, et al. Astaxanthin as a new raman probe for biosensing of specific subcellular lipidic structures: Can we detect lipids in cells under resonance conditions? [J]. Cellular and molecular life sciences : CMLS, 2021, 78(7): 3477-3484.
Bedford E E, Boujday S, Pradier C-M, et al. Spiky gold shells on magnetic particles for DNA biosensors [J]. Talanta, 2018, 182: 259-266.
Marinaro G, Coluccio M L, Gentile F. Optimization of high-density fe-au nano-arrays for surface-enhanced raman spectroscopy of biological samples [J]. Biosensors, 2021, 11(6).
Hussein M A, El-Said W A, Abu-Zied B M, et al. Nanosheet composed of gold nanoparticle/graphene/epoxy resin based on ultrasonic fabrication for flexible dopamine biosensor using surface-enhanced raman spectroscopy [J]. Nano Convergence, 2020, 7(1).
Rippa M, Sagnelli D, Vestri A, et al. Plasmonic metasurfaces for specific sers detection of shiga toxins [J]. Acs Applied Materials & Interfaces, 2022, 14(4): 4969-4979.
Jia F, Barber E, Turasan H, et al. Detection of pyocyanin using a new biodegradable sers biosensor fabricated using gold coated zein nanostructures further decorated with gold nanoparticles [J]. Journal of agricultural and food chemistry, 2019, 67(16): 4603-4610.
Díaz-Amaya S, Lin L K, Deering A J, et al. Aptamer-based sers biosensor for whole cell analytical detection of e. coli o157:H7 [J]. Analytica Chimica Acta, 2019, 1081: 146-156.
Kim S, Kim T G, Lee S H, et al. Label-free surface-enhanced raman spectroscopy biosensor for on-site breast cancer detection using human tears [J]. Acs Applied Materials & Interfaces, 2020, 12(7): 7897-7904.
Labuda J, Brett A M O, Evtugyn G, et al. Electrochemical nucleic acid-based biosensors: Concepts, terms, and methodology (iupac technical report) [J]. Pure and Applied Chemistry, 2010, 82(5): 1161-1187.
Liu X, Gao X, Yang L, et al. Metal-organic framework-functionalized paper-based electrochemical biosensor for ultrasensitive exosome assay [J]. Analytical Chemistry, 2021, 93(34): 11792-11799.
Liu D, Tang J, Xu H, et al. Split-aptamer mediated regenerable temperature-sensitive electrochemical biosensor for the detection of tumour exosomes [J]. Analytica Chimica Acta, 2022, 1219: 340027.
Lin Y, Nie B, Qu X, et al. Histostar-functionalized covalent organic framework for electrochemical detection of exosomes [J]. Biosensors, 2022, 12(9).
Dobhal G, Ayupova D, Laufersky G, et al. Cadmium-free quantum dots as fluorescent labels for exosomes [J]. Sensors (Basel, Switzerland), 2018, 18(10).
Sina A A, Vaidyanathan R, Wuethrich A, et al. Label-free detection of exosomes using a surface plasmon resonance biosensor [J]. Analytical and Bioanalytical Chemistry, 2019, 411(7): 1311-1318.
Elkady A, Hassan M, Hagag M F, et al. Innovative model of surface-enhanced raman spectroscopy for exosomes identification: An approach for the diagnosis of hepatocellular carcinoma [J]. Clinica chimica acta; international journal of clinical chemistry, 2023, 540: 117228.
Li T D, Zhang R, Chen H, et al. An ultrasensitive polydopamine bi-functionalized sers immunoassay for exosome-based diagnosis and classification of pancreatic cancer [J]. Chemical science, 2018, 9(24): 5372-5382.
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