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Title:Solitary ovarian cancer cells in the peritoneum : what happens below the surface?
Authors:ID Vos, Laura M.C. (Author)
ID Driel, Willemien J. van (Author)
ID Sonke, Gabe S. (Author)
ID Baal, Juliette O. A. M. van (Author)
ID Vijver, Koen K. van de (Author)
ID Noorden, Cornelis J. F. van (Author)
ID Lok, Christianne A. R. (Author)
Files:URL URL - Source URL, visit https://doi.org/10.1016/j.adcanc.2022.100049
 
.pdf PDF - Presentation file, download (5,53 MB)
MD5: F8921A25BC452FAB56F33F60BF32A391
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo NIB - National Institute of Biology
Abstract:Background In advanced epithelial ovarian cancer (EOC), the peritoneum is the primary site of disease recurrence which occurs in >75% of patients despite complete cytoreductive surgery (CRS) and chemotherapy. Macroscopically undetectable remaining cancer cells are deemed to be a source for recurrent disease. We investigated characteristics of occult disease in biopsies of macroscopically normal peritoneum during CRS. Materials and methods We included 14 patients with advanced stage high grade serous ovarian cancer (HGSOC). Eleven patients had received neoadjuvant chemotherapy (NACT) and three patients were chemotherapy naïve. Each patient underwent three study-related peritoneal biopsies: 1) of a metastasis, 2) adjacent to a metastasis and 3) at distance from metastases. Cryostat sections were immunohistochemically stained for PAX8 and PanCK as markers of EOC cells and for CD31 as a marker for vascular and lymphatic endothelium. The sections were analyzed semi-quantitatively. Results Macroscopically normal peritoneum showed solitary PAX8-positive cells adjacent to and at distance from metastases in all patients. Thirteen percent of these PAX8-positive cells were found to be attached to the mesothelium and are presumably spread through intra-abdominal fluid. Eighty-seven percent of the solitary PAX8-positive cells were found in the stroma underneath the mesothelium, of which 59% were firmly attached to endothelium and 33% were found in the stroma. In most cases, no sign of proliferation of the solitary cells was observed. Only a few clusters of PAX8-positive cells were found. Chemotherapy did not affect these results. Conclusions Solitary PAX8-positive cells are present in the macroscopically healthy-looking peritoneum of all EOC patients investigated, irrespective of the distance to macroscopically-visible metastases and of previous treatment. The majority of these solitary cancer cells were attached to endothelium of capillaries, venules or lymphatic vessels. Their solitary character and lack of proliferation suggests a dormant state, which could explain why these cells are unaffected by neo-adjuvant chemotherapy.
Keywords:ovarian cancer, peritoneal metastasis, translational medical research, human pathology, PAX8, cancer recurrence
Publication status:Published
Publication version:Version of Record
Publication date:01.12.2022
Year of publishing:2022
Number of pages:str. [1]-8
Numbering:Vol. 6
PID:20.500.12556/DiRROS-21551 New window
UDC:616-006
ISSN on article:2667-3940
DOI:10.1016/j.adcanc.2022.100049 New window
COBISS.SI-ID:127184643 New window
Note:Ostali avtorji: Willemien J. van Driel, Gabe S. Sonke, Juliette O. A. M. van Baal, Koen K. van de Vijver, Cornelis J. F. van Noorden, Christianne A. R. Lok; Nasl. z nasl. zaslona; Opis vira z dne 26. 10. 2022; Št. članka: 100049;
Publication date in DiRROS:26.02.2025
Views:181
Downloads:123
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Record is a part of a journal

Title:Advances in cancer biology : Metastasis
Publisher:Elsevier B.V.
ISSN:2667-3940
COBISS.SI-ID:87457795 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P1-0245-2019
Name:Ekotoksiologija, toksikološka genomika in karcinogeneza

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J3-2526-2020
Name:Razkrivanje niše matičnih glioma celic v iskanju novih terapevtskih ciljev pri bolnikih z glioblastomom

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Link:http://creativecommons.org/licenses/by-nc-nd/4.0/
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