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Article type: Research Article
Authors: Benlahfid, Mohammeda; * | Traboulsi, Waelb; c; d | Sergent, Fredericb; c; d | Benharouga, Mohamedc; d; e | Elhattabi, Khalida; f | Erguibi, Drissa; f | Karkouri, Mehdif | Elattar, Hichamg | Fadil, Abdelazizf | Fahmi, Yassinef | Aboussaouira, Touriaa; 1 | Alfaidy, Nadiab; c; d; 1
Affiliations: [a] Laboratory of Scientific and Clinical Researches in Cancerous Pathologies, Faculty of Medicine and Pharmacy, University Hassan II of Casablanca, Casablanca, Morocco | [b] Institut National de la Santé et de la Recherche Médicale U1036, Grenoble, France | [c] University Grenoble-Alpes, Grenoble, France | [d] Commissariat à l’Energie Atomique et aux Energies Alternatives, Biosciences and Biotechnology Institute of Grenoble, Grenoble, France | [e] Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5249, Laboratoire de Chimie et Biologie des Métaux, Grenoble, France | [f] Ibn Rochd University Hospital of Casablanca, University Hassan II of Casablanca, Casablanca, Morocco | [g] Laboratory of anatomopathology Moulay Driss 1er, Casablanca, Morocco
Correspondence: [*] Corresponding author: Mohammed Benlahfid, University Hassan II of Casablanca, Faculty of Medicine and Pharmacy, B.P.5696. Casablanca, Morocco. E-mail: [email protected].
Note: [1] Equal contribution.
Abstract: BACKGROUND: The highest risk factor for mortality among malignant tumors is metastasis. Endocrine gland-derived vascular endothelial growth factor (EG-VEGF) is an angiogenic factor which biological activity is mediated via two G protein-coupled receptors, prokineticin receptor1 (PROKR1) and PROKR2. Recent studies suggested that EG-VEGF expression is deregulated in multiple cancers including colorectal cancer (CRC). METHODS: Using distinctive CRC and peritoneal carcinomatosis (PC) cohorts and a corresponding control cohort, we determined the circulating levels of EG-VEGF and its in situ expression, and that of its related receptors. RESULTS: Circulating EG-VEGF levels were significantly increased in patients with metastatic PC compared to CRC and control patients (p< 0.05). Furthermore, according to clinicopathologic examinations, local EG-VEGF expression correlated with higher tumor and nodal stages (p< 0.001) of CRC. EG-VEGF and PROKR2 were highly expressed in colorectal primary lesions compared to positive controls. PROKR1 expression was lower and did not change in tumor specimens. Also, EG-VEGF and its receptor PROKR2 were differentially expressed in the colorectal primary lesions and in the control groups. CONCLUSION: Altogether these findings suggest that EG-VEGF/receptors system might be an important actor in the CRC progression into PC and might be involved in the ability of tumor cells to invade other organs. Circulating EG-VEGF could be proposed as a prognostic marker in human CRC and its progression into PC.
Keywords: Prokineticin, colorectal cancer, peritoneal carcinomatosis, EG-VEGF
DOI: 10.3233/CBM-170499
Journal: Cancer Biomarkers, vol. 21, no. 2, pp. 345-354, 2018
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