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Profile of matrix-entrapped extracellular vesicles of microenvironmental and infiltrating cell origin in decellularized colorectal cancer and adjacent mucosa.
Tassinari, Sarah; D'Angelo, Edoardo; Caicci, Federico; Grange, Cristina; Burrello, Jacopo; Fassan, Matteo; Brossa, Alessia; Bao, Riccardo Quoc; Spolverato, Gaya; Agostini, Marco; Collino, Federica; Bussolati, Benedetta.
Afiliação
  • Tassinari S; Department of Molecular Biotechnology and Health Sciences University of Torino Torino Italy.
  • D'Angelo E; General Surgery 3, Department of Surgery Oncology and Gastroenterology, University of Padova Padua Italy.
  • Caicci F; NanoInspired biomedicine lab, Fondazione Istituto di Ricerca Pediatrica Città della Speranza Padua Italy.
  • Grange C; Department of Biology University of Padova Padua Italy.
  • Burrello J; Department of Medical Science University of Torino Torino Italy.
  • Fassan M; Department of Medical Science University of Torino Torino Italy.
  • Brossa A; Department of Medicine (DIMED) University of Padua Padua Italy.
  • Bao RQ; Veneto Institute of Oncology IOV - IRCCS Padua Italy.
  • Spolverato G; Department of Molecular Biotechnology and Health Sciences University of Torino Torino Italy.
  • Agostini M; General Surgery 3, Department of Surgery Oncology and Gastroenterology, University of Padova Padua Italy.
  • Collino F; General Surgery 3, Department of Surgery Oncology and Gastroenterology, University of Padova Padua Italy.
  • Bussolati B; General Surgery 3, Department of Surgery Oncology and Gastroenterology, University of Padova Padua Italy.
J Extracell Biol ; 3(3): e144, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38939413
ABSTRACT
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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article