Department of Neurology, University of Chicago, Chicago, IL 60637, USA.
Int J Mol Sci. 2022 Aug 23;23(17):9549. doi: 10.3390/ijms23179549.
The HER2/neu signaling pathway is one of the most frequently mutated in human cancer. Although therapeutics targeting this pathway have good efficacy, cancer cells frequently develop resistance. The HER2 gene encodes the full-length HER2 protein, as well as smaller c-terminal fragments (CTFs), which have been shown to be a cause of resistance. Here, we show that HER2 CTFs, exclusive from the full-length HER2 protein, are generated via internal translation of the full-length HER2 mRNA and identify regions which are required for this mechanism to occur. These regions of the HER2 mRNA may present novel sites for therapeutic intervention via small molecules or antisense oligonucleotides (ASOs).
HER2/neu 信号通路是人类癌症中最常发生突变的通路之一。尽管针对该通路的治疗方法具有良好的疗效,但癌细胞经常会产生耐药性。HER2 基因编码全长 HER2 蛋白以及较小的 C 端片段(CTFs),这些片段已被证明是耐药的原因。在这里,我们表明全长 HER2 mRNA 的内部翻译产生了独特于全长 HER2 蛋白的 HER2 CTFs,并确定了发生这种机制所需的区域。HER2 mRNA 的这些区域可能为通过小分子或反义寡核苷酸(ASOs)进行治疗干预提供新的靶点。