Amador-Martínez Daniela, Flores Mizraim, Vargas-Castro Rafael, García-Becerra Rocío, Avila Euclides, Díaz Lorenza, García-Quiroz Janice
Departamento de Biología de La Reproducción Dr. Carlos Gual Castro, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Av. Vasco de Quiroga No. 15, Belisario Domínguez Sección XVI, Tlalpan, C.P. 14080, Ciudad de Mexico, México.
Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Av. Universidad 3000, Coyoacán, C.P. 04510, Ciudad de Mexico, México.
Nat Prod Bioprospect. 2025 Jul 3;15(1):43. doi: 10.1007/s13659-025-00528-5.
Among women, breast cancer is the most frequently diagnosed cancer and the leading cause of cancer-related mortality globally. Despite improvements in early detection and diagnosis, some risk factors have been on the rise, including the decline in birth rate, the use of oral contraceptives, and the escalation in alcohol consumption and obesity. Thus, there is an imperative urgent need to expand accessible prevention and treatment options for breast cancer. Regarding these tumors, several natural compounds have shown efficacy in slowing or preventing their progression, offering a promising therapeutic alternative. Among these, α-mangostin, a xanthone derived from mangosteen, has demonstrated promising antitumor effects against different malignancies, particularly breast cancer. The mechanisms involved in α-mangostin´s therapeutic effects include downregulation of oncogenic ion channels, modulation of cell cycle progression, suppression of oncogene expression, and interference with steroid and growth factor receptors signaling. This review thoroughly explores these mechanisms, as well as updates information on α-mangostin chemical structure and its potential as a coadjuvant to conventional breast cancer therapies. Furthermore, we provide scientifically supported insights for the development of clinically applicable α-mangostin-based treatments, highlighting the robust body of evidence supporting its cancer-fighting properties, despite the absence of clinical studies to date.
在女性中,乳腺癌是最常被诊断出的癌症,也是全球癌症相关死亡的主要原因。尽管早期检测和诊断有所改善,但一些风险因素却在上升,包括出生率下降、口服避孕药的使用、酒精消费增加和肥胖问题。因此,迫切需要扩大可及的乳腺癌预防和治疗选择。对于这些肿瘤,几种天然化合物已显示出在减缓或预防其进展方面的功效,提供了一种有前景的治疗选择。其中,α-山竹黄酮,一种从山竹中提取的氧杂蒽酮,已证明对不同恶性肿瘤,尤其是乳腺癌具有有前景的抗肿瘤作用。α-山竹黄酮治疗作用所涉及的机制包括致癌离子通道的下调、细胞周期进程的调节、癌基因表达的抑制以及对类固醇和生长因子受体信号传导的干扰。本综述全面探讨了这些机制,并更新了关于α-山竹黄酮化学结构及其作为传统乳腺癌治疗辅助剂潜力的信息。此外,尽管目前尚无临床研究,但我们为基于α-山竹黄酮的临床适用治疗方法的开发提供了有科学依据的见解,突出了支持其抗癌特性的大量证据。