Abstract

In our preliminary study, Berbamine (BA), one of the most commonly used traditional Chinese medicines, was effective in inducing the intracellular ROS levels. Since the regulation of cellular antioxidant capacity is crucial to the sensitivity of Ptx, it is feasible to propose that sensitizing cells to Ptx can be achieved through increasing the antioxidant capacity by codelivering BA. Cytotoxicity test demonstrates that either single or combinational treatment of BA and Ptx dose-dependently inhibits the proliferation of U-87 cells. Median-effect analysis clearly proves the synergistic anticancer effect between BA and Ptx. Combinational treatment of both drugs induced more intracellular ROS generation than either of the drugs did. Cotreatment of NAC could partially reverse the ROS generation and ameliorate the cytotoxicity induced by BA plus Ptx. Moreover, sequential activation of ROS-dependent phosphor-Akt expression was dose-dependently inhibited by the combinational application of BA and Ptx, which was more significantly effective than the single treatment of either BA or Ptx. Additionally, the coadministration of BA and Ptx shows the strongest tumor delaying effect in a U87 xenograft model, demonstrating the synergism between two drugs. Therefore, BA is a promising adjuvant to traditional chemotherapy, especially in combination with Ptx, to treat malignant glioma.

Highlights

  • Malignant glioma is one of the leading causes of cancerrelated mortality for patients who suffer from brain tumor all over the word [1]

  • Cultured medium (RPMI-1640), fetal bovine serum (FBS), and penicillin/streptomycin were obtained from Gibco BRL (Grand Island, NY, USA)

  • The combination index (CI) analysis (Figure 1(d)) based on the results of 48 h cytotoxicity indicated that CI values were below 1 when the two drugs were combined for 48 h incubation

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Summary

Introduction

Malignant glioma is one of the leading causes of cancerrelated mortality for patients who suffer from brain tumor all over the word [1]. Overall survival of glioma has extended because of early detection and comprehensive therapeutic regimens including operation, radiotherapy, and chemotherapy. The prognosis of malignant glioma has not been improved substantially yet due to the lack of effective adjuvant therapy with lower toxicity [2]. Paclitaxel (Ptx) has been approved by FDA to treat a series of solid tumors including breast, ovarian, gastric, and non-small cell lung cancer [3, 4]. Ptx exerts its antitumor effect through interfering with normal mitotic function by stabilizing the microtubule assembly from tubulin and preventing the depolymerization, thereby leading to a G2/M cell cycle arrest [5]. There are increasing studies demonstrating the advantage of Ptx in combination with other anticancer agents in treatment of malignant glioma [6, 7]

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