Abstract

Glioblastoma multiforme (GBM) is the most common and most aggressive malignant brain tumor. Despite optimal treatment and evolving standard of care, the median survival of patients diagnosed with GBM is only 12–15 months. In this study, we combined progesterone (PROG) and temozolomide (TMZ), a standard chemotherapeutic agent for human GBM, to test whether PROG enhances the antitumor effects of TMZ and reduces its side effects. Two WHO grade IV human GBM cells lines (U87MG and U118MG) and primary human dermal fibroblasts (HDFs) were repeatedly exposed to PROG and TMZ either alone or in combination for 3 and 6 days. Cell death was measured by MTT reduction assay. PROG and TMZ individually induced tumor cell death in a dose-dependent manner. PROG at high doses produced more cell death than TMZ alone. When combined, PROG enhanced the cell death-inducing effect of TMZ. In HDFs, PROG did not reduce viability even at the same high cytotoxic doses, but TMZ did so in a dose-dependent manner. In combination, PROG reduced TMZ toxicity in HDFs. PROG alone and in combination with TMZ suppressed the EGFR/PI3K/Akt/mTOR signaling pathway and MGMT expression in U87MG cells, thus suppressing cell proliferation. PROG and TMZ individually reduced cell migration in U87MG cells but did so more effectively in combination. PROG enhances the cytotoxic effects of TMZ in GBM cells and reduces its toxic side effects in healthy primary cells.

Highlights

  • Human glioblastoma multiforme (GBM) is a highly proliferative brain tumor

  • We investigated the individual and combined effect of PROG (5 and 80 μM) and TMZ (100 μM, the best anti-tumor dose) exposures on the proliferation of U87MG and U118MG cells using the expression of proliferating cell nuclear antigen (PCNA) as a marker of tumor cell proliferation (Fig 7A)

  • Our data can be taken to demonstrate that PROG at high doses effectively inhibits the proliferation of grade IV human GBM U87MG and U118MG cells

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Summary

Introduction

The median survival of GBM patients remains only 12–15 months despite optimal treatment including surgical resection followed by radiation and Temozolomide (TMZ)-based chemotherapy [1]. Among the several limitations of current standard of care for GBM patients are incomplete tumor resection, peri-tumoral edema, blood-brain barrier (BBB) disruption, insufficiency of the maximum radiation dose to eradicate the tumor, the toxic side effects of chemo/radio therapy, and drug resistance. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. They don’t alter the authors’ adherence to PLoS One policies on sharing data and materials

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