Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
Department of Biomedical Sciences for Health, University of Milan, 20133 Milan, Italy.
Cells. 2020 Mar 3;9(3):596. doi: 10.3390/cells9030596.
Cholangiocarcinoma (CCA) is a deadly tumor without an effective therapy. Unique metabolic and bioenergetics features are important hallmarks of tumor cells. Metabolic plasticity allows cancer cells to survive in poor nutrient environments and maximize cell growth by sustaining survival, proliferation, and metastasis. In recent years, an increasing number of studies have shown that specific signaling networks contribute to malignant tumor onset by reprogramming metabolic traits. Several evidences demonstrate that numerous metabolic mediators represent key-players of CCA progression by regulating many signaling pathways. Besides the well-known Warburg effect, several other different pathways involving carbohydrates, proteins, lipids, and nucleic acids metabolism are altered in CCA. The goal of this review is to highlight the main metabolic processes involved in the cholangio-carcinogeneis that might be considered as potential novel druggable candidates for this disease.
胆管癌(CCA)是一种致命的肿瘤,目前尚无有效的治疗方法。独特的代谢和生物能量特征是肿瘤细胞的重要标志。代谢可塑性使癌细胞能够在营养匮乏的环境中存活,并通过维持生存、增殖和转移来最大限度地促进细胞生长。近年来,越来越多的研究表明,特定的信号网络通过重编程代谢特征导致恶性肿瘤的发生。有几项证据表明,许多代谢介质通过调节许多信号通路,成为 CCA 进展的关键参与者。除了众所周知的沃伯格效应外,CCA 中还存在其他几种涉及碳水化合物、蛋白质、脂质和核酸代谢的不同途径的改变。本文综述的目的是强调参与胆管癌发生的主要代谢过程,这些过程可能被认为是该疾病潜在的新型可用药靶。