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The Therapeutic Targeting of HGF/c-Met Signaling in Hepatocellular Carcinoma: Alternative Approaches

机译:HGF / c-Met信号在肝细胞癌中的治疗靶向:替代方法

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摘要

The poor prognosis of hepatocellular carcinoma (HCC), one of the most devastating cancers worldwide, is due to frequent recurrence and metastasis. Among the metastatic factors in the tumor microenvironment, hepatocyte growth factor (HGF) has been well known to play critical roles in tumor progression, including HCC. Therefore, c-Met is now regarded as the most promising therapeutic target for the treatment of HCC. However, there are still concerns about resistance and the side effects of using conventional inhibitors of c-Met, such as tyrosine kinase inhibitors. Recently, many alternative strategies of c-Met targeting have been emerging. These include targeting the downstream effectors of c-Met, such as hydrogen peroxide-inducible clone 5 (Hic-5), to block the reactive oxygen species (ROS)-mediated signaling for HCC progression. Also, inhibition of endosomal regulators, such as PKCε and GGA3, may perturb the c-Met endosomal signaling for HCC cell migration. On the other hand, many herbal antagonists of c-Met-dependent signaling, such as saponin, resveratrol, and LZ-8, were identified. Taken together, it can be anticipated that more effective and safer c-Met targeting strategies for preventing HCC progression can be established in the future.
机译:肝细胞癌(HCC)是世界上最具破坏力的癌症之一,预后较差是由于频繁复发和转移。在肿瘤微环境中的转移因子中,众所周知,肝细胞生长因子(HGF)在包括HCC在内的肿瘤进展中起着关键作用。因此,c-Met现在被认为是治疗HCC的最有希望的治疗靶标。然而,仍然存在关于使用常规的c-Met抑制剂例如酪氨酸激酶抑制剂的抗性和副作用的担忧。最近,出现了许多针对c-Met靶向的替代策略。这些包括靶向c-Met的下游效应子,例如过氧化氢诱导的克隆5(Hic-5),以阻断活性氧(ROS)介导的HCC进程信号。同样,抑制内体调节剂,例如PKCε和GGA3,可能会干扰HCC细胞迁移的c-Met内体信号传导。另一方面,已鉴定出许多c-Met依赖性信号传导的草药拮抗剂,如皂苷,白藜芦醇和LZ-8。综上所述,可以预期,将来可以建立更有效,更安全的c-Met靶向策略来预防HCC进程。

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