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Synegic effect of paclitaxel protein-bound particles in malignant melanomas.

Research Project

Project/Area Number 15K19701
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Dermatology
Research InstitutionIwate Medical University

Principal Investigator

Watanabe Ayano  岩手医科大学, 医学部, 助教 (30740617)

Project Period (FY) 2015-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2016: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2015: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywords悪性黒色腫 / BCL2 / paclitaxel / 分子標的治療薬 / チューブリン / アブラキサン / チューブリン阻害薬 / 薬剤耐性 / ABT737
Outline of Final Research Achievements

Malignant melanoma is refractory to antitubulin agents. Treatment of the paclitaxel-resistant cell lines combined paclitaxel protein-bound particles for injectable suspension with ABT-737, an inhibitor of BCL2 and BCLxL, or simultaneous knock-down of BCL2 and BCLxL dramatically increased the cells' sensitivity, while knock-down of MCL1, another member of the BCL2 family, had only a minimal effect. Our results demonstrated the new combination therapy for malignant melanomas.

Report

(3 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report

URL: 

Published: 2015-04-16   Modified: 2018-03-22  

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