Abstract
Gliomas are the most common malignant brain tumors in adults. Bradykinin (BK) displays an important role in cancer, although the exact role of kinin receptors in the glioma biology remains unclear. This study investigated the role of kinin B1 and B2 receptors (B1R and B2R) on cell proliferation in human glioblastoma cell lineages. The mRNA expression of B1R and B2R was verified by RT-qPCR, whereas the effects of kinin agonists (des-Arg(9)-BK and BK) were analyzed by cell counting, MTT assay and annexin-V/PI determination. The PI3K/Akt and ERK1/2 signaling activation was assessed by flow cytometry. Our results demonstrated that both human glioblastoma cell lines U-138MG and U-251MG express functional B1R and B2R. The proliferative effects induced by the incubation of des-Arg(9)-BK and BK are likely related to the activation of PI3K/Akt and ERK 1/2 pathways. Moreover, the pre-incubation of the selective PI3Kγ blocker AS252424 markedly prevented kinin-induced AKT phosphorylation. Noteworthy, the selective B1R and B2R antagonists SSR240612 and HOE-140 were able to induce cell death of either lineages, with mixed apoptosis/necrosis characteristics. Taken together, the present results show that activation of B1R and B2R might contribute to glioblastoma progression in vitro. Furthermore, PI3K/Akt and ERK 1/2 signaling may be a target for adjuvant treatment of glioblastoma with a possible impact on tumor proliferation.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Apoptosis
-
Blotting, Western
-
Bradykinin / analogs & derivatives
-
Bradykinin / pharmacology
-
Bradykinin B1 Receptor Antagonists / pharmacology
-
Bradykinin B2 Receptor Antagonists / pharmacology
-
Cell Proliferation*
-
Dioxoles / pharmacology
-
Flow Cytometry
-
Glioma / drug therapy
-
Glioma / metabolism*
-
Glioma / pathology*
-
Humans
-
Mitogen-Activated Protein Kinase 1 / genetics
-
Mitogen-Activated Protein Kinase 1 / metabolism*
-
Mitogen-Activated Protein Kinase 3 / genetics
-
Mitogen-Activated Protein Kinase 3 / metabolism*
-
Phosphatidylinositol 3-Kinases / genetics
-
Phosphatidylinositol 3-Kinases / metabolism*
-
Phosphorylation / drug effects
-
Proto-Oncogene Proteins c-akt / genetics
-
Proto-Oncogene Proteins c-akt / metabolism*
-
RNA, Messenger / genetics
-
Real-Time Polymerase Chain Reaction
-
Receptor, Bradykinin B1 / chemistry
-
Receptor, Bradykinin B1 / genetics
-
Receptor, Bradykinin B1 / metabolism*
-
Receptor, Bradykinin B2 / chemistry
-
Receptor, Bradykinin B2 / genetics
-
Receptor, Bradykinin B2 / metabolism*
-
Reverse Transcriptase Polymerase Chain Reaction
-
Sulfonamides / pharmacology
-
Tumor Cells, Cultured
Substances
-
2-((3-(1,3-benzodioxol-5-yl)-3-(((6-methoxy-2-naphthyl)sulfonyl)amino)propanoyl)amino)-3-(4-((2,6-dimethylpiperidinyl)methyl)phenyl)-N-isopropyl-N-methylpropanamide
-
Bradykinin B1 Receptor Antagonists
-
Bradykinin B2 Receptor Antagonists
-
Dioxoles
-
RNA, Messenger
-
Receptor, Bradykinin B1
-
Receptor, Bradykinin B2
-
Sulfonamides
-
icatibant
-
Phosphatidylinositol 3-Kinases
-
Proto-Oncogene Proteins c-akt
-
MAPK1 protein, human
-
Mitogen-Activated Protein Kinase 1
-
Mitogen-Activated Protein Kinase 3
-
Bradykinin