小分子抑制剂治疗肝细胞癌:进展与挑战。
Small Molecule Inhibitors for Hepatocellular Carcinoma: Advances and Challenges.
机构信息
The Molecular Pharmacology Research Group, Department of Pharmacology, Toxicology and Clinical Pharmacy, Faculty of Pharmacy and Biotechnology, German University in Cairo-GUC, Cairo 11835, Egypt.
School of Life and Medical Sciences, University of Hertfordshire Hosted by Global Academic Foundation, New Administrative Capital, Cairo 11578, Egypt.
出版信息
Molecules. 2022 Aug 28;27(17):5537. doi: 10.3390/molecules27175537.
According to data provided by World Health Organization, hepatocellular carcinoma (HCC) is the sixth most common cause of deaths due to cancer worldwide. Tremendous progress has been achieved over the last 10 years developing novel agents for HCC treatment, including small-molecule kinase inhibitors. Several small molecule inhibitors currently form the core of HCC treatment due to their versatility since they would be more easily absorbed and have higher oral bioavailability, thus easier to formulate and administer to patients. In addition, they can be altered structurally to have greater volumes of distribution, allowing them to block extravascular molecular targets and to accumulate in a high concentration in the tumor microenvironment. Moreover, they can be designed to have shortened half-lives to control for immune-related adverse events. Most importantly, they would spare patients, healthcare institutions, and society as a whole from the burden of high drug costs. The present review provides an overview of the pharmaceutical compounds that are licensed for HCC treatment and other emerging compounds that are still investigated in preclinical and clinical trials. These molecules are targeting different molecular targets and pathways that are proven to be involved in the pathogenesis of the disease.
根据世界卫生组织提供的数据,肝细胞癌 (HCC) 是全球第六大常见癌症死亡原因。在过去的 10 年中,在开发 HCC 治疗的新型药物方面取得了巨大进展,包括小分子激酶抑制剂。由于小分子抑制剂具有多功能性,更容易被吸收,口服生物利用度更高,因此更容易配制并施用于患者。此外,它们可以在结构上进行改变,以具有更大的分布容积,从而能够阻断血管外的分子靶点,并在肿瘤微环境中积聚高浓度。此外,它们可以设计成半衰期更短,以控制与免疫相关的不良反应。最重要的是,它们可以使患者、医疗机构和整个社会免受高昂药物成本的负担。本综述概述了已获得 HCC 治疗许可的药物化合物以及仍在临床前和临床试验中研究的其他新兴化合物。这些分子针对不同的分子靶点和途径,这些靶点和途径已被证明与疾病的发病机制有关。