Department of Surgery, College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee.
Transplant Research Institute, James D. Eason Transplant Institute, College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee.
Mol Cancer Ther. 2023 Aug 1;22(8):936-946. doi: 10.1158/1535-7163.MCT-23-0149.
Identifying novel, unique, and personalized molecular targets for patients with pancreatic ductal adenocarcinoma (PDAC) remains the greatest challenge in altering the biology of fatal tumors. Bromo- and extra-terminal domain (BET) proteins are activated in a noncanonical fashion by TGFβ, a ubiquitous cytokine in the PDAC tumor microenvironment (TME). We hypothesized that BET inhibitors (BETi) represent a new class of drugs that attack PDAC tumors via a novel mechanism. Using a combination of patient and syngeneic murine models, we investigated the effects of the BETi drug BMS-986158 on cellular proliferation, organoid growth, cell-cycle progression, and mitochondrial metabolic disruption. These were investigated independently and in combination with standard cytotoxic chemotherapy (gemcitabine + paclitaxel [GemPTX]). BMS-986158 reduced cell viability and proliferation across multiple PDAC cell lines in a dose-dependent manner, even more so in combination with cytotoxic chemotherapy (P < 0.0001). We found that BMS-986158 reduced both human and murine PDAC organoid growth (P < 0.001), with associated perturbations in the cell cycle leading to cell-cycle arrest. BMS-986158 disrupts normal cancer-dependent mitochondrial function, leading to aberrant mitochondrial metabolism and stress via dysfunctional cellular respiration, proton leakage, and ATP production. We demonstrated mechanistic and functional data that BETi induces metabolic mitochondrial dysfunction, abrogating PDAC progression and proliferation, alone and in combination with systemic cytotoxic chemotherapies. This novel approach improves the therapeutic window in patients with PDAC and offers another treatment approach distinct from cytotoxic chemotherapy that targets cancer cell bioenergetics.
鉴定新的、独特的和个性化的分子靶点,对于改变致命肿瘤的生物学特性仍然是胰腺癌(PDAC)患者面临的最大挑战。Bromo-和末端结构域(BET)蛋白通过转化生长因子β(TGFβ)以非典型方式激活,TGFβ是 PDAC 肿瘤微环境(TME)中的一种普遍存在的细胞因子。我们假设 BET 抑制剂(BETi)代表了一类通过新机制攻击 PDAC 肿瘤的新药。我们使用患者和同基因小鼠模型的组合,研究了 BETi 药物 BMS-986158 对细胞增殖、类器官生长、细胞周期进程和线粒体代谢破坏的影响。这些影响是独立研究的,并与标准细胞毒性化疗(吉西他滨+紫杉醇[GemPTX])联合研究。BMS-986158 以剂量依赖性方式降低多种 PDAC 细胞系的细胞活力和增殖,与细胞毒性化疗联合使用时更为明显(P < 0.0001)。我们发现 BMS-986158 减少了人和鼠 PDAC 类器官的生长(P < 0.001),并伴随着细胞周期的改变,导致细胞周期停滞。BMS-986158 破坏了正常的癌症依赖的线粒体功能,导致通过功能失调的细胞呼吸、质子泄漏和 ATP 产生导致异常的线粒体代谢和应激。我们提供了机制和功能数据,表明 BETi 诱导代谢性线粒体功能障碍,单独使用和与全身细胞毒性化疗联合使用时,均可阻断 PDAC 的进展和增殖。这种新方法改善了 PDAC 患者的治疗窗口,并提供了一种与靶向癌细胞生物能量的细胞毒性化疗不同的治疗方法。