Sarah Tassinari, Edoardo D'Angelo, Federico Caicci, Cristina Grange, Jacopo Burrello, Matteo Fassan, Alessia Brossa, Riccardo Quoc Bao, Gaya Spolverato, Marco Agostini, Federica Collino, Benedetta Bussolati
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ECM-EVs in tumours and surrounding mucosa mainly expressed markers of lymphocytes, natural killer cells, antigen-presenting cells, and platelets, as well as epithelial cells, representing a multicellular microenvironment. No difference in surface marker expression was observed between tumour and mucosa ECM-EVs in stage II-III tumours. At variance, in the colon mucosa adjacent to stage IV carcinomas, ECM-EV profile showed a significantly increased level of immune, epithelial and platelet markers in comparison to the matrix of the corresponding tumour. The increase of EVs from immune cells and platelets was not observed in the mucosa adjacent to low-stage tumours. In addition, CD25, a T-lymphocyte marker, resulted specifically overexpressed by ECM-EVs from stage IV carcinomas, possibly correlated with the pro-tolerogenic environment found in the corresponding tumour tissue. These results outline the tissue microenvironmental profile of EVs in colorectal carcinoma-derived ECM and unveil a profound change in the healthy mucosa adjacent to high-stage tumours.</p>","PeriodicalId":73747,"journal":{"name":"Journal of extracellular biology","volume":"3 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jex2.144","citationCount":"0","resultStr":"{\"title\":\"Profile of matrix-entrapped extracellular vesicles of microenvironmental and infiltrating cell origin in decellularized colorectal cancer and adjacent mucosa\",\"authors\":\"Sarah Tassinari, Edoardo D'Angelo, Federico Caicci, Cristina Grange, Jacopo Burrello, Matteo Fassan, Alessia Brossa, Riccardo Quoc Bao, Gaya Spolverato, Marco Agostini, Federica Collino, Benedetta Bussolati\",\"doi\":\"10.1002/jex2.144\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Cellular elements that infiltrate and surround tumours and pre-metastatic tissues have a prominent role in tumour invasion and growth. 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At variance, in the colon mucosa adjacent to stage IV carcinomas, ECM-EV profile showed a significantly increased level of immune, epithelial and platelet markers in comparison to the matrix of the corresponding tumour. The increase of EVs from immune cells and platelets was not observed in the mucosa adjacent to low-stage tumours. In addition, CD25, a T-lymphocyte marker, resulted specifically overexpressed by ECM-EVs from stage IV carcinomas, possibly correlated with the pro-tolerogenic environment found in the corresponding tumour tissue. 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引用次数: 0
摘要
浸润和包围肿瘤及转移前组织的细胞元素在肿瘤的侵袭和生长中起着重要作用。细胞外基质(ECM-EVs)中特异性夹带和储存的细胞外基质囊泡可能反映了肿瘤微环境中的不同种群及其在肿瘤进展过程中的变化。然而,目前还不清楚它们的概况。为了阐明这一点,我们从脱细胞的结直肠癌手术标本和邻近的结肠粘膜中分离并鉴定了EVs,并分析了它们的表面标记谱。肿瘤和周围粘膜中的 ECM-EVs主要表达淋巴细胞、自然杀伤细胞、抗原递呈细胞、血小板以及上皮细胞的标记物,代表了一种多细胞微环境。在 II-III 期肿瘤中,未观察到肿瘤和粘膜 ECM-EV 表面标记物表达的差异。不同的是,在 IV 期癌邻近的结肠粘膜中,ECM-EV 图谱显示免疫、上皮和血小板标记物的水平明显高于相应肿瘤的基质。在低分期肿瘤邻近的粘膜中,未观察到免疫细胞和血小板的 EVs 增加。此外,T淋巴细胞标记物CD25在IV期癌症的ECM-EV中特异性过度表达,这可能与相应肿瘤组织中的促耐受环境有关。这些结果概述了结直肠癌衍生 ECM 中 EV 的组织微环境概况,揭示了高分期肿瘤附近健康粘膜的深刻变化。
Profile of matrix-entrapped extracellular vesicles of microenvironmental and infiltrating cell origin in decellularized colorectal cancer and adjacent mucosa
Cellular elements that infiltrate and surround tumours and pre-metastatic tissues have a prominent role in tumour invasion and growth. The extracellular vesicles specifically entrapped and stored within the extracellular matrix (ECM-EVs) may reflect the different populations of the tumour microenvironment and their change during tumour progression. However, their profile is at present unknown. To elucidate this aspect, we isolated and characterized EVs from decellularized surgical specimens of colorectal cancer and adjacent colon mucosa and analyzed their surface marker profile. ECM-EVs in tumours and surrounding mucosa mainly expressed markers of lymphocytes, natural killer cells, antigen-presenting cells, and platelets, as well as epithelial cells, representing a multicellular microenvironment. No difference in surface marker expression was observed between tumour and mucosa ECM-EVs in stage II-III tumours. At variance, in the colon mucosa adjacent to stage IV carcinomas, ECM-EV profile showed a significantly increased level of immune, epithelial and platelet markers in comparison to the matrix of the corresponding tumour. The increase of EVs from immune cells and platelets was not observed in the mucosa adjacent to low-stage tumours. In addition, CD25, a T-lymphocyte marker, resulted specifically overexpressed by ECM-EVs from stage IV carcinomas, possibly correlated with the pro-tolerogenic environment found in the corresponding tumour tissue. These results outline the tissue microenvironmental profile of EVs in colorectal carcinoma-derived ECM and unveil a profound change in the healthy mucosa adjacent to high-stage tumours.