2017
DOI: 10.1063/1.5001659
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The characterization of exosomes from biological fluids of patients with different types of cancer

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Cited by 7 publications
(4 citation statements)
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“…[31] This approach has been reported multiple times: Yunusova reports the use of CD9, CD63, CD81, and CD24 specific antibodies in order to screen EVs from biological fluids of patients suffering from varied cancers, namely stage IIIB, C ovarian cancer, T2-4N0-2M0 colorectal cancer, and stage T2-4N0-2M0 squamous cell head and neck carcinoma, thus, studying the different proteins on their surfaces by flow cytometer when the EVs were adsorbed onto latex beads. [52] Theodoraki has also used this method by immobilizing the EVs on streptavidin-labeled beads, along with a secondary detection antibodies with a fluorescent label to analyze both the proteins presented on the surface of the EV and its content (after lysis), with a LOD in the femtomolar range (Figure 2F). [31] Sharma et al have used flow cytometry to capture and characterize melanoma-derived CSPG4 + EVs present in serum samples which were subsequently used to differenti-ate between patients with early-stage cancer and patients with an advanced-stage cancer.…”
Section: Fluorescent Flow Cytometrymentioning
confidence: 99%
“…[31] This approach has been reported multiple times: Yunusova reports the use of CD9, CD63, CD81, and CD24 specific antibodies in order to screen EVs from biological fluids of patients suffering from varied cancers, namely stage IIIB, C ovarian cancer, T2-4N0-2M0 colorectal cancer, and stage T2-4N0-2M0 squamous cell head and neck carcinoma, thus, studying the different proteins on their surfaces by flow cytometer when the EVs were adsorbed onto latex beads. [52] Theodoraki has also used this method by immobilizing the EVs on streptavidin-labeled beads, along with a secondary detection antibodies with a fluorescent label to analyze both the proteins presented on the surface of the EV and its content (after lysis), with a LOD in the femtomolar range (Figure 2F). [31] Sharma et al have used flow cytometry to capture and characterize melanoma-derived CSPG4 + EVs present in serum samples which were subsequently used to differenti-ate between patients with early-stage cancer and patients with an advanced-stage cancer.…”
Section: Fluorescent Flow Cytometrymentioning
confidence: 99%
“…В настоящее время среди растворимых высокои низкомолекулярных компонентов асцита ведется активный поиск дополнительных прогностических и предикторных факторов, позволяющих уточнить молекулярный фенотип и персонифицировать лечение больных РЯ [22,29,40]. Асцитические экзосомы и микровезикулы вследствие их высокой биологической активности также вовлечены в канцерогенез [41][42][43].…”
Section: компоненты асцитической жидкости при раке яичниковunclassified
“…Источником экзосом могут быть опухолевые клетки и клетки микроокружения. Используя современные методы молекулярно-генетического анализа, возможно секвенирование всей экзосомальной ДНК, РНК, получение комплексной информации об опухоли для индивидуализации лечения и оценки риска прогрессирования [62].…”
Section: экзосомы и рак шейки маткиunclassified