Growth inhibitory effect of the somatostatin structural derivative (TT-232) on leukemia models

Miguel Tejeda, D. Gaál, O. Csuka, Gy Kéri

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

TT-232 is a structural derivative of the natural signal inhibitory peptide somatostatin, with selective antiproliferative and anti-inflammatory properties. TT-232 activates SSTR receptors (primarily the SSTR-1), which leads to irreversible cell cycle arrest, followed by secondary induction of apoptosis. TT-232 has passed phase I clinical trials without toxicity and significant side-effects. We examined the antiproliferative effect in vitro and the antitumor effect in vivo of TT-232 on leukemia cell lines. During in vivo experiments, we evaluated the therapeutic efficacy of TT-232 in various long-term administration routes; traditional injection versus infusion treatment via an inserted Alzet minipump on P-388 mice and HL-60 human leukemia models. Treatment with TT-232 started after development of the disease. In vitro, TT-232 inhibited the proliferation of P-388 mice lymphoid cells and HL-60 human promyelocytic leukemia cells in the range of 46%-97% with 24-hour treatment and 82%-100% with 48-hour treatment. Cells were treated with 30 μg/ml and 60 μg/ml dose of TT-232. With the same in vivo models, the best results were achieved when TT-232 was applied by infusion treatments. The infusion treatment with TT-232 produced 50%-80% inhibition of growth and resulted in 20%-40% long-term and leukemia-free survivors. TT-232 showed dose-, time- and administration mode-dependent antileukemia activity in vitro and in vivo, both on rodent and human models. Our results suggest that TT-232 is a promising new antileukemia agent.

Original languageEnglish
Pages (from-to)325-330
Number of pages6
JournalAnticancer research
Volume25
Issue number1 A
Publication statusPublished - Jan 1 2005

    Fingerprint

Keywords

  • Leukemia model
  • Somatostatin analog
  • TT-232

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Cite this