Wynn Michelle L, Yates Joel A, Evans Charles R, Van Wassenhove Lauren D, Wu Zhi Fen, Bridges Sydney, Bao Liwei, Fournier Chelsea, Ashrafzadeh Sepideh, Merrins Matthew J, Satin Leslie S, Schnell Santiago, Burant Charles F, Merajver Sofia D
From the Departments of Internal Medicine, Molecular and Integrative Physiology, and.
From the Departments of Internal Medicine.
J Biol Chem. 2016 Jun 24;291(26):13715-29. doi: 10.1074/jbc.M115.703959. Epub 2016 Apr 25.
Inflammatory breast cancer (IBC) is an extremely lethal cancer that rapidly metastasizes. Although the molecular attributes of IBC have been described, little is known about the underlying metabolic features of the disease. Using a variety of metabolic assays, including (13)C tracer experiments, we found that SUM149 cells, the primary in vitro model of IBC, exhibit metabolic abnormalities that distinguish them from other breast cancer cells, including elevated levels of N-acetylaspartate, a metabolite primarily associated with neuronal disorders and gliomas. Here we provide the first evidence of N-acetylaspartate in breast cancer. We also report that the oncogene RhoC, a driver of metastatic potential, modulates glutamine and N-acetylaspartate metabolism in IBC cells in vitro, revealing a novel role for RhoC as a regulator of tumor cell metabolism that extends beyond its well known role in cytoskeletal rearrangement.
炎性乳腺癌(IBC)是一种极具致死性且迅速转移的癌症。尽管已对IBC的分子特征进行了描述,但对于该疾病潜在的代谢特征却知之甚少。通过使用多种代谢分析方法,包括(13)C示踪实验,我们发现IBC的主要体外模型SUM149细胞表现出代谢异常,这使其有别于其他乳腺癌细胞,包括N-乙酰天门冬氨酸水平升高,该代谢物主要与神经疾病和神经胶质瘤相关。在此,我们提供了乳腺癌中存在N-乙酰天门冬氨酸的首个证据。我们还报告称,致癌基因RhoC作为转移潜能的驱动因子,在体外调节IBC细胞中的谷氨酰胺和N-乙酰天门冬氨酸代谢,揭示了RhoC作为肿瘤细胞代谢调节因子的新作用,这一作用超出了其在细胞骨架重排中众所周知的作用。