WISP-1 is a Wnt-1- and β-catenin-responsive oncogene

  1. Lifeng Xu1,
  2. Ryan B. Corcoran1,
  3. James W. Welsh2,
  4. Diane Pennica2, and
  5. Arnold J. Levine1,3,4
  1. 1Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544 USA; 2Department of Molecular Oncology, Genentech Inc., South San Francisco, California 94080 USA

Abstract

WISP-1 (Wnt-1 induced secreted protein 1) is a member of the CCN family of growth factors. This study identifies WISP-1 as a β-catenin-regulated gene that can contribute to tumorigenesis. The promoter of WISP-1 was cloned and shown to be activated by both Wnt-1 and β-catenin expression. TCF/LEF sites played a minor role, whereas the CREB site played an important role in this transcriptional activation. WISP-1 demonstrated oncogenic activities; overexpression of WISP-1 in normal rat kidney fibroblast cells (NRK-49F) induced morphological transformation, accelerated cell growth, and enhanced saturation density. Although these cells did not acquire anchorage-independent growth in soft agar, they readily formed tumors in nude mice, suggesting that appropriate cellular attachment is important for signaling oncogenic events downstream of WISP-1.

Keywords

Footnotes

  • 3 Present address: Rockefeller University, New York, New York 10021 USA.

  • 4 Corresponding author.

  • E-MAIL alevine{at}rockvax.rockefeller.edu; FAX (212) 327-8505.

    • Received November 16, 1999.
    • Accepted January 24, 2000.
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