4.6 Article

Derivatives of Dictyostelium differentiation-inducing factors inhibit lysophosphatidic acid-stimulated migration of murine osteosarcoma LM8 cells

期刊

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2015.06.016

关键词

Dictyostelium discoideum; DIP; Metastasis; Invasion; Osteosarcoma

资金

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan [24590110, 15K07964]
  2. Kobayashi International Scholarship Foundation
  3. Grants-in-Aid for Scientific Research [15K07964, 24590110] Funding Source: KAKEN

向作者/读者索取更多资源

Osteosarcoma is a common metastatic bone cancer that predominantly develops in children and adolescents. Metastatic osteosarcoma remains associated with a poor prognosis; therefore, more effective anti-metastatic drugs are needed. Differentiation-inducing factor-1 (DIF-1), -2, and -3 are novel lead anti-tumor agents that were originally isolated from the cellular slime mold Dictyostelium discoideum. Here we investigated the effects of a panel of DIF derivatives on lysophosphatidic acid (LPA)-induced migration of mouse osteosarcoma LM8 cells by using a Boyden chamber assay. Some DIF derivatives such as Br-DIF-1, DIF-3(+2), and Bu-DIF-3 (5-20 mu M) dose-dependefitly suppressed LPA-induced cell migration with associated IC50 values of 5.5, 4.6, and 4.2 mu M, respectively. On the other hand, the IC50 values of Br-DIF-1, DIF-3(+2), and Bu-DIF-3 versus cell proliferation were 18.5, 7.2, and 2.0 mu M, respectively, in LM8 cells, and >20, 14.8, and 4.3 mu M, respectively, in mouse 3T3-L1 fibroblasts (non-transformed). Together, our results demonstrate that Br-DIF-1 in particular may be a valuable tool for the analysis of cancer cell migration, and that DIF derivatives such as DIF-3(+2) and Bu-DIF-3 are promising lead anti-tumor agents for the development of therapies that suppress osteosarcoma cell proliferation, migration, and metastasis. (C) 2015 Elsevier Inc. All rights reserved.

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