Chang Yu-Chan, Chang Peter Mu-Hsin, Li Chien-Hsiu, Chan Ming-Hsien, Lee Yi-Jang, Chen Ming-Huang, Hsiao Michael
Department of Biomedical Imaging and Radiological Sciences, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Department of Oncology, Taipei Veterans General Hospital, Taipei, Taiwan.
Front Oncol. 2022 Jan 21;11:811635. doi: 10.3389/fonc.2021.811635. eCollection 2021.
Exposure to alkylating agents and radiation may cause damage and apoptosis in cancer cells. Meanwhile, this exposure involves resistance and leads to metabolic reprogramming to benefit cancer cells. At present, the detailed mechanism is still unclear. Based on the profiles of several transcriptomes, we found that the activity of phospholipase D (PLD) and the production of specific metabolites are related to these events. Comparing several particular inhibitors, we determined that phospholipase D1 (PLD1) plays a dominant role over other PLD members. Using the existing metabolomics platform, we demonstrated that lysophosphatidylethanolamine (LPE) and lysophosphatidylcholine (LPC) are the most critical metabolites, and are highly dependent on aldolase A (ALDOA). We further demonstrated that ALDOA could modulate total PLD enzyme activity and phosphatidic acid products. Particularly after exposure to alkylating agents and radiation, the proliferation of lung cancer cells, autophagy, and DNA repair capabilities are enhanced. The above phenotypes are closely related to the performance of the ALDOA/PLD1 axis. Moreover, we found that ALDOA inhibited PLD2 activity and enzyme function through direct protein-protein interaction (PPI) with PLD2 to enhance PLD1 and additional carcinogenic features. Most importantly, the combination of ALDOA and PLD1 can be used as an independent prognostic factor and is correlated with several clinical parameters in lung cancer. These findings indicate that, based on the PPI status between ALDOA and PLD2, a combination of radiation and/or alkylating agents with regulating ALDOA-PLD1 may be considered as a new lung cancer treatment option.
接触烷化剂和辐射可能会导致癌细胞损伤和凋亡。同时,这种接触会引发耐药性,并导致代谢重编程以利于癌细胞。目前,具体机制仍不清楚。基于多个转录组图谱,我们发现磷脂酶D(PLD)的活性和特定代谢产物的产生与这些事件有关。通过比较几种特定抑制剂,我们确定磷脂酶D1(PLD1)在其他PLD成员中起主导作用。利用现有的代谢组学平台,我们证明溶血磷脂酰乙醇胺(LPE)和溶血磷脂酰胆碱(LPC)是最关键的代谢产物,并且高度依赖醛缩酶A(ALDOA)。我们进一步证明,ALDOA可以调节总PLD酶活性和磷脂酸产物。特别是在接触烷化剂和辐射后,肺癌细胞的增殖、自噬和DNA修复能力增强。上述表型与ALDOA/PLD1轴的表现密切相关。此外,我们发现ALDOA通过与PLD2直接的蛋白质-蛋白质相互作用(PPI)抑制PLD2活性和酶功能,从而增强PLD1和其他致癌特征。最重要的是,ALDOA和PLD1的组合可作为独立的预后因素,并且与肺癌的几个临床参数相关。这些发现表明,基于ALDOA和PLD2之间的PPI状态,联合使用辐射和/或烷化剂并调节ALDOA-PLD1可被视为一种新的肺癌治疗选择。