College of Pharmacy, Al-Noor University, Mosul, Iraq.
College of MLT, Ahl Al Bayt University, Karbala, Iraq.
Med Oncol. 2024 Oct 14;41(11):271. doi: 10.1007/s12032-024-02497-0.
The most prevalent form of primary liver cancer, hepatocellular carcinoma (HCC) poses a significant global health challenge due to its limited therapeutic options. Researchers are currently focused on the complex molecular landscape that governs the initiation and progression of HCC in order to identify new avenues for diagnosis, prognosis, and treatment. In the context of HCC, the Kinesin Superfamily Proteins (KIFs) have become critical regulators of cellular processes, prompting a growing interest in their function among the diverse array of molecular actors implicated in cancer. The KIFs, a family of microtubule-based molecular motors, are renowned for their essential roles in the dynamics of mitotic spindles and intracellular transport. Beyond their well-established functions in normal cellular physiology, emerging evidence indicates that dysregulation of KIFs significantly contributes to the pathogenesis of HCC. Novel therapeutic targets and diagnostic markers are revealed through the unique opportunity to comprehend the complex interplay between KIFs and the molecular events that drive HCC.
原发性肝癌中最常见的形式是肝细胞癌 (HCC),由于其治疗选择有限,因此对全球健康构成了重大挑战。研究人员目前专注于控制 HCC 发生和发展的复杂分子谱,以确定新的诊断、预后和治疗途径。在 HCC 中,驱动蛋白超家族蛋白 (KIFs) 已成为细胞过程的关键调节剂,促使人们对其在众多涉及癌症的分子因素中的功能产生了越来越大的兴趣。KIFs 是一类基于微管的分子马达,以其在有丝分裂纺锤体和细胞内运输动力学中的重要作用而闻名。除了其在正常细胞生理学中的既定功能外,新出现的证据表明 KIFs 的失调对 HCC 的发病机制有重大贡献。通过了解 KIFs 与驱动 HCC 的分子事件之间的复杂相互作用,揭示了新的治疗靶点和诊断标志物。