Jacobo-Herrera Nadia, Pérez-Plasencia Carlos, Castro-Torres Víctor Alberto, Martínez-Vázquez Mariano, González-Esquinca Alma Rosa, Zentella-Dehesa Alejandro
Unidad de Bioquímica, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubiran, Ciudad de México, Mexico.
Laboratorio de Genómica Funcional, Unidad de Biomedicina, Facultad de Estudios Superiores (FES) Iztacala, Universidad Nacional Autónoma de México (UNAM), Tlalnepantla, Mexico.
Front Pharmacol. 2019 Jul 18;10:783. doi: 10.3389/fphar.2019.00783. eCollection 2019.
The Kingdom Plantae has provided several successful drugs for the treatment of different diseases, including cancer, and continues to be a source of new possible therapeutic molecules. For example, the annonaceous acetogenins (AAs) are secondary metabolites found in the Annonaceae family, which are plants employed in traditional medicine for the treatment of cancer and various other diseases. These polyketides are inhibitors of Complex I in the respiratory chain of tumor cells, a process that is closely related to tumor metabolism, cell death, apoptosis, and autophagy. The goal of this review is to update readers on the role of the AAs as antitumor agents using and studies to demonstrate their importance in the area of oncology drug discovery. For this purpose, we performed a literature search in the PubMed scientific database using a range of keywords, including acetogenins and cancer, acetogenins antitumor activity, acetogenins and cytotoxicity, and acetogenins mechanism of action, among others. As a result, we found that the AAs are cytotoxic compounds that can induce apoptosis, cell cycle arrest, and autophagy , in addition to exhibiting tumor growth inhibition . The functional group related to their antineoplastic activity is suggested to be the mono or bis tetrahydrofuran ring accompanied by two or more hydroxy groups. The versatility of the AA bioactivity therefore renders them potential therapeutic agents for cancer treatment. It is therefore apparent that nature is worth further examination to aid in the discovery of more effective, accurate, and less harmful therapies in the fight against cancer.
植物界已经提供了几种成功用于治疗包括癌症在内的不同疾病的药物,并且仍然是新的潜在治疗分子的来源。例如,番荔枝科产乙酸物(AAs)是在番荔枝科植物中发现的次生代谢产物,这些植物在传统医学中用于治疗癌症和各种其他疾病。这些聚酮化合物是肿瘤细胞呼吸链中复合体I的抑制剂,这一过程与肿瘤代谢、细胞死亡、细胞凋亡和自噬密切相关。本综述的目的是通过 和 研究,向读者介绍AAs作为抗肿瘤药物的作用,以证明它们在肿瘤学药物发现领域的重要性。为此,我们在PubMed科学数据库中使用了一系列关键词进行文献检索,包括产乙酸物与癌症、产乙酸物的抗肿瘤活性、产乙酸物与细胞毒性以及产乙酸物的作用机制等。结果,我们发现AAs是细胞毒性化合物,除了具有抑制肿瘤生长的作用外,还能诱导细胞凋亡、细胞周期阻滞和自噬 。与其抗肿瘤活性相关的官能团被认为是带有两个或更多羟基的单或双四氢呋喃环。因此,AA生物活性的多样性使其成为癌症治疗的潜在治疗剂。因此,显然值得对自然进行进一步研究,以帮助发现更有效、准确且危害更小的抗癌疗法。