Kashyap Vivek K, Sharma Bhuvnesh P, Pandey Divya, Singh Ajay K, Peasah-Darkwah Godwin, Singh Bhupesh, Roy Kuldeep K, Yallapu Murali M, Chauhan Subhash C
Division of Cancer Immunology and Microbiology, Medicine, and Oncology Integrated Service Unit, School of Medicine, University of Texas Rio Grande Valley, McAllen, TX 78504, USA.
South Texas Center of Excellence in Cancer Research (ST-CECR), McAllen, TX 78504, USA.
Cells. 2024 Dec 12;13(24):2053. doi: 10.3390/cells13242053.
Metarrestin (ML246) is a first-in-class pyrrole-pyrimidine-derived small molecule that selectively targets the perinucleolar compartment (PNC). PNC is a distinct subnuclear structure predominantly found in solid tumor cells. The occurrence of PNC demonstrates a positive correlation with malignancy, serving as an indicator of tumor aggressiveness, progression, and metastasis. Various promising preclinical results have led to the clinical translation of metarrestin into a first-in-human trial. This review aims to summarize (i) the current understanding of the structure and function of PNC and its role in cancer progression and metastasis, (ii) key findings from studies examining the effect of metarrestin on various cancers across the translational spectrum, including in vitro, in vivo, and human clinical trial studies, and (iii) the pharmaceutical relevance of metarrestin as a promising anticancer candidate. Furthermore, our molecular docking and MD simulation studies show that metarrestin binds to eEF1A1 and eEF1A2 with a strong and stable affinity and inhibits eEF1A2 more efficiently compared to eEF1A1. The promising results from preclinical studies suggest that metarrestin has the potential to revolutionize the treatment of cancer, heralding a paradigm shift in its therapeutic management.
美他瑞司汀(ML246)是一种新型的源自吡咯 - 嘧啶的小分子,它选择性地靶向核仁周区(PNC)。PNC是一种独特的亚核结构,主要存在于实体瘤细胞中。PNC的出现与恶性肿瘤呈正相关,可作为肿瘤侵袭性、进展和转移的指标。各种有前景的临床前研究结果已促使美他瑞司汀进入首次人体试验的临床转化阶段。本综述旨在总结:(i)目前对PNC的结构和功能及其在癌症进展和转移中的作用的理解;(ii)研究美他瑞司汀对跨转化谱的各种癌症的影响的研究的关键发现,包括体外、体内和人体临床试验研究;(iii)美他瑞司汀作为一种有前景的抗癌候选药物的药学相关性。此外,我们的分子对接和分子动力学模拟研究表明,美他瑞司汀以强而稳定的亲和力与eEF1A1和eEF1A2结合,并且与eEF1A1相比,能更有效地抑制eEF1A2。临床前研究的有前景结果表明,美他瑞司汀有可能彻底改变癌症治疗方式,预示着其治疗管理的范式转变。