The Angiogenic Activity of Ascites in the Course of Ovarian Cancer as a Marker of Disease Progression

Author:

Gawrychowski Krzysztof1,Szewczyk Grzegorz23ORCID,Skopińska-Różewska Ewa4,Małecki Maciej56,Barcz Ewa7,Kamiński Paweł7,Miedzińska-Maciejewska Magdalena8,Śmiertka Wacław9,Szukiewicz Dariusz3ORCID,Skopiński Piotr10

Affiliation:

1. Department of Gynecological Oncology and Oncology, Medicover Hospital, Rzeczypospolitej 5, 02-972 Warsaw, Poland

2. Department of Obstetrics and Gynecology, Institute of Mother and Child, Kasprzaka 17A, 01-211 Warsaw, Poland

3. Department of General and Experimental Pathology, Warsaw Medical University, Pawińskiego 3C, 02-106 Warsaw, Poland

4. Department of Pathology, Centre of Biostructure Research, Warsaw Medical University, Chałubińskiego 5, 02-004 Warsaw, Poland

5. Department of Applied Pharmacy and Bioengineering, Warsaw Medical University, Warsaw, Poland

6. Institute of Mother and Child, Kasprzaka 17A, 01-211 Warsaw, Poland

7. 1st Department of Obstetrics and Gynecology, Warsaw Medical University, Pl. Starynkiewicza 1, 02-015 Warsaw, Poland

8. Department of Surgical Oncology, Holy Family Hospital, Madalińskiego 25, 02-544 Warsaw, Poland

9. Department of Oncology, National Institute of Oncology, Wawelska 15, 02-034 Warsaw, Poland

10. Department of Histology and Embryology, Centre of Biostructure Research, Warsaw Medical University, Chałubińskiego 5, 02-004 Warsaw, Poland

Abstract

Ovarian cancer cells are able to create invasive implants in the peritoneum and their growth is directly associated with the angiogenetic potential. This effect is probably stimulated by vascular endothelial growth factor (VEGF) and interleukin-8 (IL-8), which are both found in ascites. The aim of this study was to assess the influence of ascites produced by ovarian cancer on the angiogenesis. Peritoneal fluid was collected from patients with advanced ovarian cancer; cancer cells were separated from CD45+ leukocytes. Angiogenesis was assessed in mice, after intradermal injection of full cellular suspension together with supernatant or phosphate buffered saline, purified cancer cells suspension, or CD45+ leukocytes suspension. The angiogenesis index (AI) was assessed after 72 hours. VEGF and Il-8 were measured in the supernatant and cellular suspension. AI was the highest in the isolated cancer cells suspensions as well in the group stimulated with supernatant. Both VEGF and IL-8 were high in supernatants from ascites rich in cancer cells (>45%). A significant correlation was revealed between IL-8 concentration and AI. We conclude that ascites in patients with advanced ovarian cancer stimulates angiogenesis and this mechanism is dependent mostly on cancer cells activity and enhanced by cooperation with infiltrating leukocytes.

Publisher

Hindawi Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics,Molecular Biology,General Medicine

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