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Title:Poor perfusion of the microvasculature in peritoneal metastases of ovarian cancer
Authors:ID Kastelein, Arnoud W. (Author)
ID Vos, Laura M.C. (Author)
ID Baal, Juliette O. A. M. van (Author)
ID Koning, Jasper J. (Author)
ID Hira, Vashendriya V. V. (Author)
ID Nieuwland, Rienk (Author)
ID Driel, Willemien J. van (Author)
ID Uz, Zühre (Author)
ID Gulik, Thomas M van (Author)
ID Rheenen, Jacco van (Author)
ID Ince, Can (Author)
ID Roovers, Jan-Paul W.R. (Author)
ID Noorden, Cornelis J. F. van (Author)
ID Lok, Christianne A. R. (Author)
Files:.pdf PDF - Presentation file, download (1,65 MB)
MD5: E498C1F660C211C21B12C520662E4CED
 
URL URL - Source URL, visit https://doi.org/10.1007/s10585-020-10024-4
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo NIB - National Institute of Biology
Abstract:Most women with epithelial ovarian cancer (EOC) suffer from peritoneal carcinomatosis upon first clinical presentation. Extensive peritoneal carcinomatosis has a poor prognosis and its pathophysiology is not well understood. Although treatment with systemic intravenous chemotherapy is often initially successful, peritoneal recurrences occur regularly. We hypothesized that insufficient or poorly-perfused microvasculature may impair the therapeutic efficacy of systemic intravenous chemotherapy but may also limit expansive and invasive growth characteristic of peritoneal EOC metastases. In 23 patients with advanced EOC or suspicion thereof, we determined the angioarchitecture and perfusion of the microvasculature in peritoneum and in peritoneal metastases using incident dark field (IDF) imaging. Additionally, we performed immunohistochemical analysis and 3-dimensional (3D) whole tumor imaging using light sheet fluorescence microscopy of IDF-imaged tissue sites. In all metastases, microvasculature was present but the angioarchitecture was chaotic and the vessel density and perfusion of vessels was significantly lower than in unaffected peritoneum. Immunohistochemical analysis showed expression of vascular endothelial growth factor and hypoxia inducible factor 1α, and 3D imaging demonstrated vascular continuity between metastases and the vascular network of the peritoneum beneath the elastic lamina of the peritoneum. We conclude that perfusion of the microvasculature within metastases is limited, which may cause hypoxia, affect the behavior of EOC metastases on the peritoneum and limit the response of EOC metastases to systemic treatment.
Keywords:microvasculature, microcirculation, EOC, peritoneal carcinomatosa, incident dark feld imaging
Publication status:Published
Publication version:Version of Record
Publication date:01.02.2020
Year of publishing:2020
Number of pages:str. 293-304
Numbering:37
PID:20.500.12556/DiRROS-19549 New window
UDC:577
ISSN on article:0262-0898
DOI:10.1007/s10585-020-10024-4 New window
COBISS.SI-ID:40667909 New window
Publication date in DiRROS:23.07.2024
Views:315
Downloads:233
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Record is a part of a journal

Title:Clinical & experimental metastasis
Shortened title:Clin. exp. metastasis
Publisher:Springer
ISSN:0262-0898
COBISS.SI-ID:25229056 New window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Secondary language

Language:Slovenian
Keywords:mikrovaskulatura, mikrocirkulacija, EOC, karcinomatoza peritone


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