Irinotecan Upregulates Fibroblast Growth Factor Receptor 3 Expression in Colorectal Cancer Cells, Which Mitigates Irinotecan-Induced Apoptosis12

نویسندگان

  • Zeynep N. Erdem
  • Stefanie Schwarz
  • Daniel Drev
  • Christine Heinzle
  • Andrea Reti
  • Petra Heffeter
  • Xenia Hudec
  • Klaus Holzmann
  • Bettina Grasl-Kraupp
  • Walter Berger
  • Michael Grusch
  • Brigitte Marian
چکیده

BACKGROUND Irinotecan (IRI) is an integral part of colorectal cancer (CRC) therapy, but response rates are unsatisfactory and resistance mechanisms are still insufficiently understood. As fibroblast growth factor receptor 3 (FGFR3) mediates essential survival signals in CRC, it is a candidate gene for causing intrinsic resistance to IRI. METHODS We have used cell line models overexpressing FGFR3 to study the receptor's impact on IRI response. For pathway blockade, a dominant-negative receptor mutant and a small molecule kinase inhibitor were employed. RESULTS IRI exposure induced expression of FGFR3 as well as its ligands FGF8 and FGF18 both in cell cultures and in xenograft tumors. As overexpression of FGFR3 mitigated IRI-induced apoptosis in CRC cell models, this suggests that the drug itself activated a survival response. On the cellular level, the antiapoptotic protein bcl-xl was upregulated and caspase 3 activation was inhibited. Targeting FGFR3 signaling using a dominant-negative receptor mutant sensitized cells for IRI. In addition, the FGFR inhibitor PD173074 acted synergistically with the chemotherapeutic drug and significantly enhanced IRI-induced caspase 3 activity in vitro. In vivo, PD173074 strongly inhibited growth of IRI-treated tumors. CONCLUSION Together, our results indicate that targeting FGFR3 can be a promising strategy to enhance IRI response in CRC patients.

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عنوان ژورنال:

دوره 10  شماره 

صفحات  -

تاریخ انتشار 2017