論文

査読有り
2014年2月

Sialic acid-binding lectin (leczyme) induces apoptosis to malignant mesothelioma and exerts synergistic antitumor effects with TRAIL

INTERNATIONAL JOURNAL OF ONCOLOGY
  • Takeo Tatsuta
  • ,
  • Masahiro Hosono
  • ,
  • Kohta Takahashi
  • ,
  • Takashi Omoto
  • ,
  • Yukiko Kariya
  • ,
  • Shigeki Sugawara
  • ,
  • Senitiroh Hakomori
  • ,
  • Kazuo Nitta

44
2
開始ページ
377
終了ページ
384
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.3892/ijo.2013.2192
出版者・発行元
SPANDIDOS PUBL LTD

Malignant mesothelioma is a highly aggressive tumor with poor prognosis. An effective drug for treatment of malignant mesothelioma is greatly needed. Sialic acid-binding lectin (SBL) isolated from oocytes of Rana catesbeiana is a multifunctional protein which has lectin activity, ribonuclease activity and antitumor activity, so it could be developed as a new type of anticancer drug. The validity of SBL for treatment of malignant mesothelioma was assessed using three malignant mesotheliomas and a non-malignant mesothlial cell line. Effectiveness of combinatorial treatment of SBL and tumor necrosis factor-related apoptosis inducing ligand (TRAIL) was also elucidated and characterized. SBL induced tumor-selective cytotoxicity that was attributed to induction of apoptosis. Combinatorial treatment of SBL and TRAIL showed synergistic apoptosis-inducing effect. Additional experiments revealed that Bid was the mediating molecule for the synergistic effect in SBL and TRAIL. These results suggested that SBL could be a promising candidate for the therapeutics for malignant mesothelioma. Furthermore, the combinatorial treatment of SBL and TRAIL could be an effective regimen against malignant mesothelioma.

リンク情報
DOI
https://doi.org/10.3892/ijo.2013.2192
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/24297392
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000332687400004&DestApp=WOS_CPL
ID情報
  • DOI : 10.3892/ijo.2013.2192
  • ISSN : 1019-6439
  • eISSN : 1791-2423
  • PubMed ID : 24297392
  • Web of Science ID : WOS:000332687400004

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