Combination of a STAT3 Inhibitor and an mTOR Inhibitor Against a Temozolomide-resistant Glioblastoma Cell Line.

نویسندگان

  • Haruo Miyata
  • Tadashi Ashizawa
  • Akira Iizuka
  • Ryota Kondou
  • Chizu Nonomura
  • Takashi Sugino
  • Kenichi Urakami
  • Akira Asai
  • Nakamasa Hayashi
  • Koichi Mitsuya
  • Yoko Nakasu
  • Ken Yamaguchi
  • Yasuto Akiyama
چکیده

BACKGROUND Temozolomide-resistant (TMZ-R) glioblastoma is very difficult to treat, and a novel approach to overcome resistance is needed. MATERIALS AND METHODS The efficacy of a combination treatment of STAT3 inhibitor, STX-0119, with rapamycin was investigated against our established TMZ-resistant U87 cell line. RESULTS The growth-inhibitory effect of the combination treatment was significant against the TMZ-R U87 cell line (IC50: 78 μM for STX-0119, 30.5 μM for rapamycin and 11.3 μM for combination of the two). Western blotting analysis demonstrated that the inhibitory effect of STX-0119 on S6 and 4E-BP1 activation through regulation of YKL-40 expression occurred in addition to the inhibitory effect of rapamycin against the mTOR pathway. CONCLUSION These results suggest that the STAT3 pathway is associated with the mTOR downstream pathway mediated by YKL-40 protein, and the combination therapy of the STAT3 inhibitor and rapamycin could be worth developing as a novel therapeutic approach against TMZ-resistant relapsed gliomas.

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عنوان ژورنال:
  • Cancer genomics & proteomics

دوره 14 1  شماره 

صفحات  -

تاریخ انتشار 2017