Targeting NUCKS1 with a fragment of tRNAAsn(GUU) of Chinese yew for the treatment of colorectal cancer

IF 5.9 3区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Kai-Yue Cao , Da Zhang , Long-Bo Bai , Tong-Meng Yan , Yan Chen , Yu-Yang Jiang , Zhi-Hong Jiang
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引用次数: 0

Abstract

Despite the discovery of numerous oncogenes in colorectal cancer (CRC), the development of associated drugs is limited, posing a significant challenge for CRC treatment. Identification of novel druggable targets is therefore crucial for the therapeutic development of CRC. Here, we report the first investigation on therapeutics targeting the potent oncogene NUCKS1 to suppress cancer progression. NUCKS1-orientated bioinformatics screening of NUCKS1 inhibitors from our library of tRNA fragments originated from medicinal plants identified tRF-T36, a 5′ tRNA fragment of tRNAAsn(GUU) of Chinese yew (Taxus chinensis), exhibiting stronger inhibitory effects than taxol against CRC progression. Mechanistically, tRF-T36 binds directly to the 3′ UTR of NUCKS1 mRNA to downregulate its expressions via RNAi pathway. High-throughput RNA sequencing indicated that the downregulated NUCKS1 induced by tRF-T36 further inhibits PI3K/Akt pathway, as verified by the significantly efficacy decrease of tRF-T36 mimic in co-treatment with 740Y-P, an agonist of PI3K/Akt pathway. Collectively, our findings emphasize the importance of NUCKS1 as a promising druggable target for CRC. Furthermore, the present study provides the first siRNA sequence, tRF-T36 mimic, as small RNA drug candidate, thereby shedding light on CRC therapeutics.
利用红豆杉tRNAAsn(GUU)片段靶向NUCKS1治疗结直肠癌。
尽管在结直肠癌(CRC)中发现了许多致癌基因,但相关药物的开发有限,这给结直肠癌的治疗带来了重大挑战。因此,确定新的药物靶点对结直肠癌的治疗发展至关重要。在这里,我们报告了针对强效致癌基因NUCKS1抑制癌症进展的治疗方法的首次研究。对药用植物tRNA片段库中的NUCKS1抑制剂进行了以NUCKS1为导向的生物信息学筛选,鉴定出红豆杉(Taxus chinensis) tRNAAsn(GUU)的5' tRNA片段tRF-T36,其对结直肠癌进展的抑制作用强于紫杉醇。机制上,tRF-T36直接结合到NUCKS1 mRNA的3' UTR上,通过RNAi途径下调其表达。高通量RNA测序结果表明,tRF-T36诱导的下调NUCKS1进一步抑制PI3K/Akt通路,这一点通过tRF-T36模拟物与PI3K/Akt通路激动剂740Y-P共处理时的疗效显著降低得到证实。总的来说,我们的研究结果强调了NUCKS1作为CRC有希望的药物靶点的重要性。此外,本研究提供了第一个siRNA序列,tRF-T36模拟物,作为小RNA候选药物,从而为结直肠癌治疗提供了线索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Non-coding RNA Research
Non-coding RNA Research Medicine-Biochemistry (medical)
CiteScore
7.70
自引率
6.00%
发文量
39
审稿时长
49 days
期刊介绍: Non-coding RNA Research aims to publish high quality research and review articles on the mechanistic role of non-coding RNAs in all human diseases. This interdisciplinary journal will welcome research dealing with all aspects of non-coding RNAs-their biogenesis, regulation and role in disease progression. The focus of this journal will be to publish translational studies as well as well-designed basic studies with translational and clinical implications. The non-coding RNAs of particular interest will be microRNAs (miRNAs), small interfering RNAs (siRNAs), small nucleolar RNAs (snoRNAs), U-RNAs/small nuclear RNAs (snRNAs), exosomal/extracellular RNAs (exRNAs), Piwi-interacting RNAs (piRNAs) and long non-coding RNAs. Topics of interest will include, but not limited to: -Regulation of non-coding RNAs -Targets and regulatory functions of non-coding RNAs -Epigenetics and non-coding RNAs -Biological functions of non-coding RNAs -Non-coding RNAs as biomarkers -Non-coding RNA-based therapeutics -Prognostic value of non-coding RNAs -Pharmacological studies involving non-coding RNAs -Population based and epidemiological studies -Gene expression / proteomics / computational / pathway analysis-based studies on non-coding RNAs with functional validation -Novel strategies to manipulate non-coding RNAs expression and function -Clinical studies on evaluation of non-coding RNAs The journal will strive to disseminate cutting edge research, showcasing the ever-evolving importance of non-coding RNAs in modern day research and medicine.
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