FEBS Open Bio (Nov 2020)

Combined use of irinotecan and p53 activator enhances growth inhibition of mesothelioma cells

  • Bo Han,
  • Hyeon‐Cheol Lee‐Okada,
  • Momoko Ishimine,
  • Hajime Orita,
  • Keiko Nishikawa,
  • Tetsuya Takagaki,
  • Kazunori Kajino,
  • Takehiko Yokomizo,
  • Okio Hino,
  • Toshiyuki Kobayashi

DOI
https://doi.org/10.1002/2211-5463.12985
Journal volume & issue
Vol. 10, no. 11
pp. 2375 – 2387

Abstract

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Malignant mesothelioma (MM) is an aggressive malignant neoplasm which rapidly invades pleural tissues and has a poor prognosis. Here, we explore enhancement of the effect of irinotecan [camptothecin‐11 (CPT‐11)] by the p53‐dependent induction of carboxylesterase 2 (CES2), a CPT‐11‐activating enzyme, in MM. The level of CES2 mRNA was greatly increased on treatment with nutlin‐3a. A combination of CPT‐11 and nutlin‐3a inhibited the growth of MM cells more effectively than either drug alone. Knocking down CES2 in MM cells reduced the effect of the drug combination, and its forced expression in MESO4 cells enhanced the growth inhibitory activity of CPT‐11 in the absence of nutlin‐3a. Enhancement of the growth inhibitory activity of CPT‐11 by nutlin‐3a suggests a possible new combinatorial MM chemotherapy regimen.

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