Tan Yinfei, Sementino Eleonora, Chernoff Jonathan, Testa Joseph R
Cancer Biology Program, Fox Chase Cancer CenterPhiladelphia, Pennsylvania, USA.
Am J Cancer Res. 2017 Aug 1;7(8):1724-1737. eCollection 2017.
Clinical management of malignant mesothelioma (MM) is very challenging due to marked resistance of this tumor to chemotherapy. Various mechanisms lead to a less than ideal drug concentration inside of MM cells, diminishing cytotoxicity. Consequently, single cytotoxic drugs achieve very modest response rates in MM patients, and combination regimens using standard and novel therapies have achieved only limited improvement in overall survival. Here, we demonstrate that MYC has either proliferative or pro-survival effects in MM cells during normal or stressed conditions, respectively. A MYC inhibitor 10058-F4 reduced MM cell proliferation via down regulation of cyclin D. Under serum starvation conditions, MM cells became quiescent, and the addition of MYC inhibitors triggered apoptosis in the resting MM cells. We also found that high concentrations of the PAK inhibitor PF3758309 killed MM cells, but the drug had only cytostatic effects at lower concentrations. These quiescent cells underwent apoptosis upon pharmacological inhibition of MYC. A novel MYC inhibitor KJ-Pyr-9 and a newer PAK inhibitor, FRAX597, also demonstrated marked cytotoxic cooperativity. Collectively, these findings demonstrate that targeting of MYC can sensitize MM cells and provide rationale for inhibition of MYC and PAK as a novel combinatory regimen for the treatment of this otherwise therapy-resistant, clinically incurable malignancy.
恶性间皮瘤(MM)的临床管理极具挑战性,因为这种肿瘤对化疗具有显著抗性。多种机制导致MM细胞内的药物浓度不理想,从而降低细胞毒性。因此,单一细胞毒性药物在MM患者中取得的缓解率非常低,而使用标准疗法和新疗法的联合方案在总生存期方面仅取得了有限的改善。在此,我们证明MYC在正常或应激条件下分别对MM细胞具有增殖或促生存作用。一种MYC抑制剂10058 - F4通过下调细胞周期蛋白D来降低MM细胞增殖。在血清饥饿条件下,MM细胞进入静止状态,添加MYC抑制剂会触发静止MM细胞的凋亡。我们还发现高浓度的PAK抑制剂PF3758309可杀死MM细胞,但该药物在较低浓度时仅具有细胞抑制作用。这些静止细胞在MYC受到药理学抑制后会发生凋亡。一种新型MYC抑制剂KJ - Pyr - 9和一种更新的PAK抑制剂FRAX597也显示出显著的细胞毒性协同作用。总体而言,这些发现表明靶向MYC可使MM细胞敏感化,并为抑制MYC和PAK作为治疗这种原本具有抗药性、临床无法治愈的恶性肿瘤的新型联合方案提供了理论依据。