Anticancer Properties of Baicalin against Breast Cancer and other Gynecological Cancers: Therapeutic Opportunities based on Underlying Mechanisms.

Mohammad Hossein Pourhanifeh, Hossein Farrokhi-Kebria, Parsa Mostanadi, Tahereh Farkhondeh, Saeed Samarghandian
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Abstract

Gynecological cancers are serious life-threatening diseases responsible for high morbidity and mortality around the world. Chemotherapy, radiotherapy, and surgery are considered standard therapeutic modalities for these cancers. Since the mentioned treatments have undesirable side effects and are not effective enough, further attempts are required to explore potent complementary and/or alternative treatments. This study was designed to review and discuss the anticancer potentials of baicalin against gynecological cancers based on causal mechanisms and underlying pathways. Traditional medicine has been used for thousands of years in the therapy of diverse human diseases. The therapeutic effects of natural compounds like baicalin have been widely investigated in cancer therapy. Baicalin was effective against gynecological cancers by regulating key cellular mechanisms, including apoptosis, autophagy, and angiogenesis. Baicalin exerted its anticancer property by regulating most molecular signaling pathways, including PI3K/Akt/mTOR, NFκB, MAPK/ERK, and Wnt/β-catenin. However, more numerous experimental and clinical studies should be designed to find the efficacy of baicalin and the related mechanisms of action.

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黄芩苷对乳腺癌和其他妇科癌症的抗癌特性:基于基本机制的治疗机会。
妇科癌症是严重威胁生命的疾病,在全世界都有很高的发病率和死亡率。化疗、放疗和手术被认为是治疗这些癌症的标准方法。由于上述治疗方法存在不良副作用且不够有效,因此需要进一步尝试探索有效的补充和/或替代治疗方法。本研究旨在根据黄芩苷的成因机制和潜在途径,回顾和讨论黄芩苷对妇科癌症的抗癌潜力。几千年来,传统医学一直被用于治疗人类的各种疾病。黄芩苷等天然化合物在癌症治疗中的疗效已得到广泛研究。黄芩苷通过调节关键的细胞机制,包括细胞凋亡、自噬和血管生成,对妇科癌症有效。黄芩苷通过调节大多数分子信号通路(包括 PI3K/Akt/mTOR、NFκB、MAPK/ERK 和 Wnt/β-catenin)发挥抗癌作用。然而,要找到黄芩苷的功效和相关作用机制,还需要进行更多的实验和临床研究。
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