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A natural peptide, dolastatin 15, induces G2/M cell cycle arrest and apoptosis of human multiple myeloma cells.

Abstract
Several anti-cancer agents are derivative from natural products and microorganisms. The dolastatins are natural peptides derived from the marine mollusc Dolabella auricularia, which have recently been reported as an anti-cancer agent. Dolastatin 10 and 15 are small peptides; most preclinical studies have used dolastatin 10. It has been reported that dolastatins have cytotoxic activity by inhibiting microtubule assembly, and several clinical studies have already begun for solid tumors. However, the effects of dolastatin 15 against hematological malignancies such as myeloma cells have never been reported. We demonstrate here for the first time that dolastatin 15 induces cell cycle arrest at the G2/M phase followed by apoptosis in various human myeloma cell lines (RPMI8226, U266, and IM9), suggesting that it has effects on mitotic spindles. In addition, we showed that dolastatin 15 induces apoptosis of myeloma cells via activation of both mitochondrial- and Fas (CD95)/Fas-L (CD95-L)-mediated pathways. Our investigations have identified a novel inhibitor of microtubule assembly that induces mitotic arrest and apoptosis of myeloma cells. Therefore, it is possible that dolastatin 15 might be a novel and safe therapeutic agent for patients with multiple myeloma.
AuthorsMasanori Sato, Morihiko Sagawa, Tomonori Nakazato, Yasuo Ikeda, Masahiro Kizaki
JournalInternational journal of oncology (Int J Oncol) Vol. 30 Issue 6 Pg. 1453-9 (Jun 2007) ISSN: 1019-6439 [Print] Greece
PMID17487366 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • Depsipeptides
  • Fas Ligand Protein
  • fas Receptor
  • dolastatin 15
Topics
  • Antineoplastic Agents (pharmacology)
  • Apoptosis (drug effects)
  • Blotting, Western
  • Cell Cycle (drug effects)
  • Cell Division (drug effects)
  • Depsipeptides (pharmacology)
  • Fas Ligand Protein (metabolism)
  • G2 Phase (drug effects)
  • Humans
  • Mitochondria (drug effects)
  • Multiple Myeloma (drug therapy)
  • fas Receptor (metabolism)

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