Regular Article
Marked Induction of the IAP Family Antiapoptotic Proteins Survivin and XIAP by VEGF in Vascular Endothelial Cells

https://doi.org/10.1006/bbrc.1999.1589Get rights and content

Abstract

Vascular endothelial growth factor (VEGF) is a potent angiogenic factor that has been shown to act as an endothelial cell mitogen as well as a vascular permeability factor. Several recent reports have also implicated VEGF as a major survival factor for endothelial cells during angiogenesis and vasculogenesis along with other growth factors such as bFGF and angiopoietin-1. VEGF has been shown to mediate this additional function, at least in part through the induction of bcl-2 and the activation of the PI3 kinase-Akt/PKB signaling pathway. We report here that VEGF can also mediate the induction/upregulation of members of a newly discovered family of antiapoptotic proteins, namely the Inhibitors of Apoptosis (IAP), in vascular endothelial cells. We show that VEGF165 leads to the induction of XIAP (2.9-fold) and survivin (19.1-fold) protein in human umbilical vein endothelial cells (HUVECs). In contrast, bFGF had little effect on XIAP expression, but produced approximately a 10-fold induction on survivin. VEGF-dependent upregulation of survivin could be prevented by cell cycle arrest in the G1 and S phases. These findings implicate that the survival and mitotic functions of VEGF in an angiogenic context may be more intrinsically related than previously anticipated. Moreover, they also raise the possibility of therapeutically targeting XIAP or survivin in antiangiogenic therapy as a means of suppressing tumor growth, in addition to directly targeting tumor cells which express these survival proteins.

References (33)

  • D. Hanahan et al.

    Cell

    (1996)
  • M. Klagsbrun et al.

    Curr. Biol.

    (1993)
  • P. Carmeliet et al.

    Cell

    (1999)
  • H.P. Gerber et al.

    J. Biol. Chem.

    (1998)
  • K. Gupta et al.

    Exp. Cell Res

    (1999)
  • G. Ambrosini et al.

    J. Biol. Chem.

    (1998)
  • L.K. Miller

    Trends Cell Biol.

    (1999)
  • A.J. Horrevoets et al.

    Blood

    (1999)
  • H.P. Gerber et al.

    J. Biol. Chem.

    (1998)
  • G. Neufeld et al.

    FASEB J.

    (1999)
  • L.E. Benjamin et al.

    J. Clin. Invest.

    (1999)
  • T. Alon et al.

    Nature Med.

    (1995)
  • L.E. Benjamin et al.

    Proc. Natl. Acad. Sci. USA

    (1997)
  • J.E. Nor et al.

    Am. J. Pathol.

    (1999)
  • P. Liston et al.

    Nature

    (1996)
  • E.C. LaCasse et al.

    Oncogene

    (1998)
  • Cited by (308)

    • The Multiple Roles of the IAP Super-family in cancer

      2020, Pharmacology and Therapeutics
    • Nanomedicine-based combination anticancer therapy between nucleic acids and small-molecular drugs

      2017, Advanced Drug Delivery Reviews
      Citation Excerpt :

      Ryan et al. demonstrated that survivin is an attractive target for anti-cancer therapy because of its role in poor prognosis and aggressiveness of the tumors [137]. Survivin enhances angiogenesis, the mechanism which is likely to be related to its ability to inhibit apoptosis in endothelial cells, thereby enhancing cell survival [138–140]. Furthermore, increased expression of survivin has also been found to confer resistance to chemotherapy [141,142].

    • Pleiotropic effects of survivin in vascular endothelial cells

      2016, Microvascular Research
      Citation Excerpt :

      Although minimally expressed in normal adult tissues, SVV is highly expressed in embryonic tissues and various types of human cancers, and its expression is correlated with poor cancer prognosis (Altieri, 2001; Balakier et al., 2013; Hoffman et al., 2002). In vascular endothelial cells, SVV expression is significantly boosted in response to platelet-derived growth factor (PDGF), VEGF, angiopoietin, as well as vascular injury (Blanc-Brude et al., 2002; Papapetropoulos et al., 2000; Tran et al., 1999). Functionally, SVV stimulates endothelial cell proliferation while inhibiting apoptosisin endothelial cells (Blanc-Brude et al., 2002).

    • Lymphangioleiomyomatosis (LAM): Molecular Insights into mTOR Regulation Lead to Targeted Therapies

      2016, Molecules to Medicine with mTOR: Translating Critical Pathways into Novel Therapeutic Strategies
    View all citing articles on Scopus
    1

    To whom correspondence should be addressed. Fax: (416) 480-5703. E-mail: [email protected].

    View full text