Host kinin B1 receptor plays a protective role against melanoma progression

Host kinin B1 receptor plays a protective role against melanoma progression

Author Maria, Andrea G. Google Scholar
Dillenburg-Pilla, Patricia Google Scholar
Reis, Rosana I. Google Scholar
Floriano, Elaine M. Google Scholar
Tefe-Silva, Cristiane Google Scholar
Ramos, Simone G. Google Scholar
Pesquero, Joao B. Autor UNIFESP Google Scholar
Nahmias, Clara Google Scholar
Costa-Neto, Claudio M. Google Scholar
Abstract Melanoma is a very aggressive tumor that arises from melanocytes. Late stage and widely spread diseases do not respond to standard therapeutic approaches. The kallikrein-kinin system (KKS) participates in biological processes such as vasodilatation, pain and inflammatory response. However, the role of KKS in tumor formation and progression is not completely understood. The role of the host kinin B1 receptor in melanoma development was evaluated using a syngeneic melanoma model. Primary tumors and metastasis were respectively induced by injecting B16F10 melanoma cells, which are derived from C57BL/6 mice, subcutaneously or in the tail vein in wild type C57BL/6 and B1 receptor knockout mice (B1(-/-)). Tumors developed in B1(-/-) mice presented unfavorable prognostic factors such as increased incidence of ulceration, higher levels of IL-10, higher activation of proliferative pathways such as ERK1/2 and Akt, and increased mitotic index. Furthermore, in the metastasis model, B1(-/-) mice developed larger metastatic colonies in the lung and lower CD8(+) immune effector cells when compared with WT animals. Altogether, our results provide evidences that B1(-/-) animals developed primary tumors with multiple features associated with poor prognosis and unfavorable metastatic onset, indicating that the B1 receptor may contribute to improve the host response against melanoma progression.
xmlui.dri2xhtml.METS-1.0.item-coverage London
Language English
Sponsor Sao Paulo State Research Foundation (FAPESP)
Grant number FAPESP: 2010/13346-4
FAPESP: 2012/20148-0
FAPESP: 2011/02144-4
Date 2016
Published in Scientific Reports. London, v. 6, p. -, 2016.
ISSN 2045-2322 (Sherpa/Romeo, impact factor)
Publisher Nature Publishing Group
Extent -
Access rights Open access Open Access
Type Article
Web of Science ID WOS:000370518700001

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