Department of Cancer Biology, University of Toledo Health Science Campus, Toledo, Ohio.
Department of Pharmacology & Experimental Therapeutics, University of Toledo Health Science Campus, Toledo, Ohio.
Cancer Rep (Hoboken). 2022 Dec;5(12):e1299. doi: 10.1002/cnr2.1299. Epub 2020 Oct 14.
In cap-dependent translation, the eukaryotic translation initiation factor 4A (eIF4A1) is an mRNA helicase is involved in unwinding of the secondary structure, such as the stem-loops, at the 5'-leader regions of the key oncogenic mRNAs. This facilitates ribosomal scanning and translation of the oncogenic mRNAs. eIF4A1 has a regulatory role in translating many oncoproteins that have vital roles in several steps of metastases. Sridharan et. al. have discovered and provide a novel insight into how eIF4A1 can play a regulatory role in drug resistance by influencing the levels of pluripotent Yamanaka transcription factors and ATP-binding cassette (ABC) transporters in triple-negative breast cancer (TNBC) stem-like cells. These findings may help us understand the molecular underpinnings of chemoresistance, especially in established metastases in TNBC. Importantly, eIF4A1 may form a novel clinical target in metastatic TNBC and the drug eFT226 from Effector Therapeutics targeting eIF4A1 is already in phase1-2 clinical trial.
在帽依赖性翻译中,真核翻译起始因子 4A(eIF4A1)是一种 mRNA 解旋酶,参与解开关键致癌 mRNA 的 5'-先导区的二级结构,如茎环。这有助于核糖体扫描和致癌 mRNA 的翻译。eIF4A1 在翻译许多癌蛋白中具有调节作用,这些癌蛋白在转移的几个步骤中具有重要作用。Sridharan 等人发现并提供了新的见解,即 eIF4A1 如何通过影响三阴性乳腺癌(TNBC)干细胞样细胞中的多能 Yamanaka 转录因子和 ATP 结合盒(ABC)转运蛋白的水平来发挥调节作用。这些发现可能有助于我们理解化疗耐药的分子基础,特别是在 TNBC 中的已建立转移中。重要的是,eIF4A1 可能成为转移性 TNBC 的新临床靶点,Effector Therapeutics 公司的靶向 eIF4A1 的药物 eFT226 已经在进行 1-2 期临床试验。