Kaushal Shruti, Gupta Samriddhi, Shefrin Seyad, Vora Dhvani Sandip, Kaul Sunil C, Sundar Durai, Wadhwa Renu, Dhanjal Jaspreet Kaur
Department of Computational Biology, Indraprastha Institute of Information Technology (IIIT) Delhi, Okhla Industrial Estate, Phase III, New Delhi 110020, India.
Department of Biochemical Engineering and Biotechnology, Indian Institute of Technology (IIT) Delhi, New Delhi 110016, India.
Cancers (Basel). 2024 Oct 13;16(20):3470. doi: 10.3390/cancers16203470.
Upregulation of stress chaperone Mortalin has been closely linked to the malignant transformation of cells, tumorigenesis, the progression of tumors to highly aggressive stages, metastasis, drug resistance, and relapse. Various in vitro and in vivo assays have provided evidence of the critical role of Mortalin upregulation in promoting cancer cell characteristics, including proliferation, migration, invasion, and the inhibition of apoptosis, a consistent feature of most cancers. Given its critical role in several steps in oncogenesis and multi-modes of action, Mortalin presents a promising target for cancer therapy. Consequently, Mortalin inhibitors are emerging as potential anti-cancer drugs. In this review, we discuss various inhibitors of Mortalin (peptides, small RNAs, natural and synthetic compounds, and antibodies), elucidating their anti-cancer potentials.
应激伴侣分子 mortalin 的上调与细胞的恶性转化、肿瘤发生、肿瘤进展至高度侵袭性阶段、转移、耐药性及复发密切相关。各种体外和体内试验均已证明 mortalin 上调在促进癌细胞特性(包括增殖、迁移、侵袭及抑制细胞凋亡,这是大多数癌症的一个共同特征)方面的关键作用。鉴于其在肿瘤发生的多个步骤及多种作用模式中的关键作用,mortalin 是一个很有前景的癌症治疗靶点。因此,mortalin 抑制剂正成为潜在的抗癌药物。在本综述中,我们讨论了 mortalin 的各种抑制剂(肽、小 RNA、天然和合成化合物以及抗体),阐明了它们的抗癌潜力。