Hyperthermia inhibits recombination repair of gemcitabine-stalled replication forks

Mustafa Raoof, Cihui Zhu, Brandon T. Cisneros, Heping Liu, Stuart J. Corr, Lon J. Wilson, Steven A. Curley

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

Background: Gemcitabine is a potent nucleoside analogue against solid tumors, but development of drug resistance is a substantial problem. Removal of gemcitabine incorporated into DNA by repair mechanisms may contribute to resistance in chemo-refractory solid tumors. Human hepatocellular carcinoma (HCC) is usually very chemoresistant to gemcitabine.

Methods: We treated HCC in vitro and in vivo (orthotopic murine model with human Hep3B or HepG2 xenografts, 7-10 CB17SCID mice per group) with gemcitabine. The role of homologous recombination repair proteins in repairing stalled replication forks was evaluated with hyperthermia exposure and cell-cycle analysis. The Student t-test was used for two-sample comparisons. Multiple group data were analyzed using one-way analysis of variance. All statistical tests were two-sided.

Results: We demonstrated that Mre11-mediated homologous recombination repair of gemcitabine-stalled replication forks is crucial to survival of HCC cells. Furthermore, we demonstrated inhibition of Mre11 by an exonuclease inhibitor or concomitant hyperthermia. In orthotopic murine models of chemoresistant HCC, the Hep3B tumor mass with radiofrequency plus gemcitabine treatment (mean ± SD, 180 ± 91 mg) was statistically significantly smaller compared with gemcitabine alone (661 ± 419 mg, P = .0063).

Conclusions: This study provides mechanistic understanding of homologous recombination inhibiting-strategies, such as noninvasive radiofrequency field-induced hyperthermia, to overcome resistance to gemcitabine in refractory human solid tumors.

Original languageEnglish (US)
JournalJournal of the National Cancer Institute
Volume106
Issue number8
DOIs
StatePublished - Aug 1 2014

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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