Cross-talk between vascular endothelial growth factor and semaphorin-3A pathway in the regulation of normal and malignant mesothelial cell proliferation

Luca Tamagnone, Alfonso Catalano, Paola Caprari, Sabrina Rodilossi, Piergiacomo Betta, Mario Castellucci, Andrea Casazza, Antonio Procopio

Risultato della ricerca: Contributo in rivistaArticolo in rivista

68 Citazioni (Scopus)

Abstract

Vascular endothelial growth factor (VEGF) and semaphorin-3A (Sema-3A) play important roles in the transduction of promitotic and antimitotic signals, respectively. Here, we report that these conflicting signals are integrated via negative feedback between VEGF and Sema-3A pathways in several primary normal, but not malignant, mesothelial cells. Unlike malignant mesothelial (MM) cells, in which VEGF induces cell proliferation, normal mesothelial (NM) cell growth was repressed by VEGF. Although both cell-types expressed an overlapping set of VEGF tyrosine-kinase receptors, only in NM cells VEGF exposure entails a p38 mitogen-activated protein kinase (MAPK)-dependent increased of Sema-3A production. Inhibition of p38 MAPK (by SB202190 and SB203580) or a dominant-negative mutant of Sema-3A receptor plexin-A1 reversed the inhibitory effects of VEGF in NM cells, increasing cyclin D1 synthesis and cell growth. Conversely, sustained activation of p38 MAPK by the p38 MAPK-activating kinases MKK3 and MKK6 or transfection with Sema-3A inhibited VEGF-induced cyclin D1 up-regulation and MM cell proliferation. Therefore, these results delineate a new role of Sema-3A in VEGF function mediated by p38 MAPK and suggest that the abrogation of regulated Sema-3A expression is responsible for VEGF-driven growth of tumor cells.
Lingua originaleEnglish
pagine (da-a)1-20
Numero di pagine20
RivistaFASEB JOURNAL
Volume18
DOI
Stato di pubblicazionePubblicato - 2004

Keywords

  • MESOTHELIOMA
  • MESOTHELIUM
  • SEMA-3A
  • VEGF
  • p38 MAPK

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