Wu Jung-Ju, Chen Shu-Hsin, Lee Chien-Hsing, Li Yi-Zhen, Hsu Yu-Wei, Hsieh Ming-Ying, Lee Ying-Ray
Department of Chinese Medicine, Ditmanson Medical Foundation Chia-Yi Christian Hospital Chiayi 600, Taiwan.
Department of Medical Research, Ditmanson Medical Foundation Chia-Yi Christian Hospital Chiayi 600, Taiwan.
Am J Cancer Res. 2024 Jul 15;14(7):3317-3334. doi: 10.62347/MINX1330. eCollection 2024.
Thyroid cancer (TC) stands out as the most prevalent endocrine malignancy globally, with a steadily increasing incidence. Its clinical manifestations include enlarged thyroid nodules, dysphagia, enophthalmos, and various other symptoms. While standard treatments such as thyroidectomy and radioiodine therapy effectively manage most cases of differentiated thyroid cancers (DTC), some recurrent cases of DTC or those involving poorly differentiated thyroid cancers (PDTC) require specialized interventions. However, existing drugs primarily address symptom management without offering a curative solution. Therefore, the development of a new therapeutic agent for these challenging cases is of utmost importance. Flavopereirine, derived from , has demonstrated promise as a potential anti-cancer agent across various human cancers. However, its specific anti-cancer effects on human thyroid cancer (TC) have remained unclear. Therefore, this study aims to investigate the anti-cancer activity of flavopereirine in human TC. The research findings revealed that flavopereirine effectively hinders the growth of human TC cells, induces cell cycle arrest, promotes apoptosis, and modulates autophagy. Moreover, the study delved into the underlying mechanisms by which flavopereirine influenced signaling pathways. To validate these anti-cancer effects, an zebrafish model was utilized, confirming the efficacy of flavopereirine against human TC cells. In summary, this study establishes that flavopereirine exhibits notable anti-human TC activities, positioning it as a promising therapeutic candidate for the treatment of human thyroid cancer.
甲状腺癌(TC)是全球最常见的内分泌恶性肿瘤,其发病率呈稳步上升趋势。其临床表现包括甲状腺结节肿大、吞咽困难、眼球突出及其他各种症状。虽然甲状腺切除术和放射性碘治疗等标准治疗方法能有效治疗大多数分化型甲状腺癌(DTC)病例,但一些DTC复发病例或低分化甲状腺癌(PDTC)病例需要特殊干预。然而,现有药物主要是缓解症状,无法治愈。因此,开发一种针对这些具有挑战性病例的新型治疗药物至关重要。从[来源未提及]提取的黄佩瑞林,在多种人类癌症中已显示出作为潜在抗癌药物的前景。然而,其对人类甲状腺癌(TC)的具体抗癌作用仍不清楚。因此,本研究旨在探讨黄佩瑞林对人类TC的抗癌活性。研究结果表明,黄佩瑞林能有效抑制人类TC细胞的生长,诱导细胞周期停滞,促进细胞凋亡,并调节自噬。此外,该研究深入探究了黄佩瑞林影响信号通路的潜在机制。为验证这些抗癌作用,使用了斑马鱼模型,证实了黄佩瑞林对人类TC细胞的疗效。总之,本研究证实黄佩瑞林具有显著的抗人类TC活性,使其成为治疗人类甲状腺癌的有前景的治疗候选药物。