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2013 Fiscal Year Final Research Report

Molecular basis of melanomagenesis based on the failure of pluripotency maintenance of melanocyte stem cells

Research Project

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Project/Area Number 23591612
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Dermatology
Research InstitutionAkita University

Principal Investigator

MANABE Motomu  秋田大学, 医学(系)研究科(研究院), 教授 (30138309)

Project Period (FY) 2011 – 2013
Keywordsメラノーマ / スフェロイド / 三酸化ヒ素 / サリノマイシン
Research Abstract

Recurrence after chemotherapy is a major cause of cancer mortality: subsets of tumor cells evade initial chemotherapy or radiotherapy and survive to re-propagate the tumor. To develop a novel therapeutic approach for melanoma, we applied a non-adhesive culture system which developed spheroids mimicking the properties of melanoma in vivo. Subsequently, spheroids involved cells exhibiting clonogenic and slow-cycling properties in addition to chemotherapeutic resistance to doxorubicin. Interestingly, while treatment of spheroids with either salinomycin or As2O3 showed limiting effects, a combinatorial treatment was markedly superior to single treatment with each drug. Thus, melanoma spheroids could be a new platform for studying melanoma biology and are likely to provide a clinically relevant target for the novel chemotherapy.

  • Research Products

    (1 results)

All 2013

All Journal Article (1 results)

  • [Journal Article] Salinomycin sensitizes melanoma spheroids containing slow-cycling cells to the effects of arsenic trioxide2013

    • Author(s)
      Ishikawa N,Takahashi M,Noguchi N,Manabe M
    • Journal Title

      Akita J Med

      Volume: 40 Pages: 143-150

URL: 

Published: 2015-07-16  

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