School of Chinese Medicine, Hong Kong Baptist University, Hong Kong SAR, China.
Shenzhen Kivita Innovative Drug Discovery Institute, Nanshan District, Shenzhen, China.
Curr Med Chem. 2018;25(38):5007-5056. doi: 10.2174/0929867324666171006131927.
Cancer is a leading cause of mortality in the world and metastasis is to blame. A number of naphthoquinones (NQs) have shown ability to reduce cancer stemness and metastatic potential. Furano-naphthoquinones (FNQs), which is a class of NQ characterized by the incorporation of an additional furan ring, have demonstrated improved anti-cancer potency as compared to the other classes of NQs.
In this study, the natural origins, synthetic routes and derivatives of migrastatic NQs were reviewed. The anti-invasive and anti-metastatic mechanisms of NQs and the more powerful FNQs in targeting cancer were also discussed.
The articles related to the anti-invasive mechanisms of NQs were comprehensively reviewed. The plant origins, synthetic routes and antitumor effects of more than 360 FNQs were also covered and presented according to their chemical structures.
Anti-cancer NQs inhibit cancer invasion by acting on epithelial-mesenchymal transition (EMT), cancer stem cells (CSCs) and signal transducer and activator of transcription 3 (STAT3) signaling. BBI608, a natural FNQ, has entered phases I and II clinical trials. It has been regarded as a potential candidate for new-generation lead compound acting directly on CSCs to overcome the problem of chemotherapy resistance. Apart from the plant-derived FNQs, there are a number of synthetic FNQs that were found to intervene in cancer invasion and metastasis.
The anti-invasive mechanisms of NQs have been thoroughly studied. FNQs generally show higher anti-cancer activity than that of NQs. The mechanisms of action of FNQs are worth further investigation.
癌症是世界上主要的死亡原因,而转移是罪魁祸首。许多萘醌(NQs)已显示出降低癌症干性和转移潜力的能力。呋喃萘醌(FNQs)是一类 NQ,其特征是包含一个额外的呋喃环,与其他 NQ 类相比,表现出更好的抗癌活性。
本研究综述了具有迁移抑制作用的 NQs 的天然来源、合成途径和衍生物。还讨论了 NQs 的抗侵袭和抗转移机制以及 FNQs 在靶向癌症方面的更强作用。
全面综述了与 NQs 抗侵袭机制相关的文章。还根据其化学结构综述了超过 360 种 FNQs 的植物来源、合成途径和抗肿瘤作用。
抗癌 NQs 通过作用于上皮-间充质转化(EMT)、癌症干细胞(CSCs)和信号转导和转录激活因子 3(STAT3)信号来抑制癌症侵袭。BBI608 是一种天然 FNQ,已进入 I 期和 II 期临床试验。它被认为是一种有前途的候选药物,可直接作用于 CSCs,以克服化疗耐药性问题。除了植物来源的 FNQs 外,还有许多合成的 FNQs 被发现可以干预癌症的侵袭和转移。
已经深入研究了 NQs 的抗侵袭机制。FNQs 通常比 NQs 具有更高的抗癌活性。FNQs 的作用机制值得进一步研究。