The receptor super-antagonist Sant7: A potent and safe inhibitor of IL-6 on human myeloma cells (review)

Rocco Savino, Anna Demartis, Laura Ciapponi, Elisabetta Sporeno, Carlo Toniatti, Francesca Bernassola, Gennaro Melino, Bernard Klein, Gennaro Ciliberto

Research output: Contribution to journalArticle

Abstract

Interleukin-6 (IL-6) plays a central role in the pathogenesis of multiple myeloma, acting both as a growth and a survival factor for myeloma cells. IL-6 has been recently shown to possess three topologically distinct receptor binding sites: site 1 for binding to the subunit specific chain IL-6Rα and sites 2 and 3 for the interaction with two separate subunits of the signalling chain gp130. We have generated a set of IL-6 receptor antagonists carrying substitutions that abolish interaction with gp130 at either site 2 alone (site 2 antagonist) or at both sites 2 and 3 (site 2+3 antagonist). In addition, substitutions were introduced at site 1 that increased affinity for IL-6Rα. When tested as growth inhibitors on a representative set of IL-6-dependent human myeloma cell lines (XG-1, XG-2, XG-4 and XG-6), although site 2 antagonists were effective on 3 out of 4 of the cell lines, only the site 2+3 antagonist Sant7 showed full antagonism on the entire spectrum of cells tested. Moreover, IL-6 receptor antagonists were also proapoptotic factors for myeloma cells. Their capacity to induce cell death was directly related to the impairment of binding to gp130 and to their ability to fully block intracellular signalling. In fact, the most potent inducer of apoptosis was again Sant7, which also counteracted the protective autocrine effect excercised by the endogenously produced IL-6. On the basis of these results we propose the super-antagonist Sant7 as a possible candidate for the immunotherapy of multiple myeloma.

Original languageEnglish
Pages (from-to)485-492
Number of pages8
JournalOncology Reports
Volume4
Issue number3
Publication statusPublished - May 1997

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Keywords

  • antagonist
  • apoptosis
  • interleukin-6
  • multiple myeloma

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

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