Non-cell-autonomous signaling by Shh in tumors: challenges and opportunities for therapeutic targets

Expert Opin Ther Targets. 2010 Jul;14(7):693-702. doi: 10.1517/14728222.2010.497488.

Abstract

Importance of the field: The Hedgehog (Hh) pathway is required during many developmental events; in adults the Hedgehog pathway is involved in the maintenance of several stem cell niches. It is therefore not surprising that aberrantly regulated Hh pathway activity can cause birth defects in the developing organism, as well as neoplastic disease later in life.

Areas covered in this review: As a consequence of the involvement in pathogenesis, the Hh pathway components are subject to an intense scrutiny as potential targets for therapeutic agents. We aim to provide an overview of the biology of the Hh proteins and the cellular response, in conjunction with potential therapeutic interventions.

What the reader will gain: Specifically, we focus on the recently discovered non-cell-autonomous Shh signaling used by tumors and the implications of this for the design of treatment strategies. This should provide the reader with up-to-date knowledge on the role of the Hh pathway in tumor progression and the options to treat these malignancies.

Take home message: An important concept that we advocate in this review is the need to recognize the need to target both the stromal and the tumor compartment in malignancies that rely on paracrine Shh signaling.

Publication types

  • Review

MeSH terms

  • Acylation / drug effects
  • Animals
  • Antineoplastic Agents / pharmacology
  • Endocytosis / drug effects
  • Hedgehog Proteins / antagonists & inhibitors
  • Hedgehog Proteins / metabolism
  • Hedgehog Proteins / physiology*
  • Humans
  • Intercellular Signaling Peptides and Proteins / physiology
  • Ligands
  • Neoplasms / drug therapy*
  • Neoplasms / physiopathology*
  • Paracrine Communication* / drug effects
  • Paracrine Communication* / physiology
  • Protein Processing, Post-Translational
  • Secretory Pathway / drug effects
  • Stem Cell Niche / drug effects
  • Stem Cell Niche / physiopathology
  • Stromal Cells / drug effects
  • Stromal Cells / physiology

Substances

  • Antineoplastic Agents
  • Hedgehog Proteins
  • Intercellular Signaling Peptides and Proteins
  • Ligands
  • SHH protein, human