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    <subfield code="a">10.3390/cancers15092479</subfield>
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    <subfield code="2">sideral</subfield>
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    <subfield code="a">ART-2023-133812</subfield>
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    <subfield code="a">Sancho-Albero, María</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-8762-5457</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">X-ray Photoelectron Spectroscopy (XPS) analysis of nitrogen environment in small extracellular vesicle membranes: a potential novel technique with application for cancer screening</subfield>
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    <subfield code="c">2023</subfield>
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    <subfield code="a">Small extracellular vesicle (EV) membranes display characteristic protein-lipidic composition features that are related to their cell of origin, providing valuable clues regarding their parental cell composition and real-time state. This could be especially interesting in the case of cancer cell-derived EVs, as their membranes could serve as valuable tools in liquid biopsy applications and to detect changes in the tumor malignancy. X-Ray Photoelectron Spectroscopy (XPS) is a powerful surface analysis technique able to detect every chemical element present, being also sensitive to their chemical environment. Here we explore the use of XPS as a fast technique to characterize EV membrane composition, with possible application in cancer research. Notably, we have focused on the nitrogen environment as an indicator of the relative abundance of pyridine-type bonding, primary, secondary and tertiary amines. Specifically, we have analyzed how tumoral and healthy cells have different nitrogen chemical environments that can indicate the presence or absence of malignancy. In addition, a collection of human serum samples from cancer patients and healthy donors was also analyzed. The differential XPS analysis of EVs collected from patients confirmed that the patterns of amine evolution could be related to markers of cancer disease, opening the possibility of their use as a non-invasive blood biomarker.</subfield>
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    <subfield code="9">info:eu-repo/grantAgreement/ES/DGA-FEDER/Una manera de hacer Europa</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/DGA-FSE/Building Europe from Aragon</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/EC/H2020/742684/EU/Catalytic Dual-Function Devices Against Cancer/CADENCE</subfield>
    <subfield code="9">This project has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No H2020 742684-CADENCE</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/ISCIII DTS21-00130</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/ISCIII/PI19-01007</subfield>
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    <subfield code="b">78 / 322 = 0.242</subfield>
    <subfield code="c">2023</subfield>
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    <subfield code="a">Oncology</subfield>
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    <subfield code="a">Cancer Research</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Martín-Pardillos, Ana</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
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    <subfield code="a">Irusta, Silvia</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-2966-9088</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Sebastián, Víctor</subfield>
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    <subfield code="a">Cebolla, Vicente Luis</subfield>
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    <subfield code="a">Santamaría, Jesús</subfield>
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    <subfield code="b">Dpto. Cirugía</subfield>
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    <subfield code="a">Universidad de Zaragoza</subfield>
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    <subfield code="g">15, 9 (2023), 2479 [18 pp.]</subfield>
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