Sorafenib for hepatocellular carcinoma: potential molecular targets and resistance mechanisms.

Mandeep Dahiya, Harish Dureja
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引用次数: 4

Abstract

Hepatocellular carcinoma (HCC) is the most widespread typical therapy-resistant, unresectable type of malignant solid tumour with a high death rate constituting huge medical concern. Sorafenib is a small molecule oral multi-target kinase potent inhibitor that acts by suppressing/blocking the multiplication of the tumour cells, angiogenesis, and encouraging apoptosis of the tumour cells. Though, the precise mechanism of tumour cell death induction by sorafenib is yet under exploration. Furthermore, genetic heterogeneity plays a critical role in developing sorafenib resistance, which leads the way to identify the need for predictive biomarkers responsible for drug resistance. Therefore, it is essential to find out the fundamental resistance mechanisms to expand therapeutic plans. The authors summarize the molecular concepts of resistance, progression, potential molecular targets, HCC management therapies, and discussion on the advancements expected in the coming future, inclusive of biomarker-driven treatment strategies, which may provide the prospects to design innovative therapeutically targeted strategies for the HCC treatment and the clinical implementation of emerging targeted agents.

索拉非尼治疗肝细胞癌:潜在分子靶点和耐药机制
肝细胞癌(HCC)是最广泛的典型的耐药、不可切除的恶性实体瘤,其高死亡率引起了巨大的医学关注。索拉非尼是一种小分子口服多靶点激酶抑制剂,其作用是抑制/阻断肿瘤细胞的增殖、血管生成和促进肿瘤细胞的凋亡。然而,索拉非尼诱导肿瘤细胞死亡的确切机制仍在探索中。此外,遗传异质性在索拉非尼耐药的发展中起着关键作用,这导致了确定耐药预测性生物标志物的需求。因此,有必要找出基本的耐药机制,以扩大治疗计划。作者总结了耐药、进展、潜在的分子靶点、HCC管理治疗的分子概念,并讨论了未来的进展,包括生物标志物驱动的治疗策略,这可能为HCC治疗设计创新的靶向治疗策略和新兴靶向药物的临床实施提供前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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