Department of Medical Oncology, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, 266000, China.
Department of Oncology, Peking University International Hospital, Peking University, Beijing, 102206, China.
Biomark Med. 2021 May;15(7):497-508. doi: 10.2217/bmm-2020-0464. Epub 2021 Mar 26.
There was increasing evidence showing that ARID1A alterations correlated with higher tumor mutational burden, but there were limited studies focusing on the adaptive mechanisms for tumor cells to survive under excessive genomic alterations. To further explore the adaptive mechanisms under ARID1A alterations, we performed RNA sequencing in ARID1A knockdown hepatocellular carcinoma cell lines, and demonstrated that decreased expression of ARID1A controlled global ribosomal proteins synthesis. The results were further confirmed by quantitative reverse transcription-PCR and bioinformatic analysis in The Cancer Genome Atlas Liver Hepatocellular Carcinoma database. The present study was the first to demonstrate that ARID1A might be involved in the translation pathway and served as an adaptive mechanism for tumor cells to survive under stress.
越来越多的证据表明,ARID1A 改变与更高的肿瘤突变负担相关,但针对肿瘤细胞在过度基因组改变下生存的适应性机制的研究有限。为了进一步探索 ARID1A 改变下的适应性机制,我们在 ARID1A 敲低的肝癌细胞系中进行了 RNA 测序,结果表明 ARID1A 的表达下调控制了全局核糖体蛋白的合成。这些结果在 The Cancer Genome Atlas Liver Hepatocellular Carcinoma 数据库中的定量逆转录-PCR 和生物信息学分析中得到了进一步证实。本研究首次证明 ARID1A 可能参与翻译途径,并作为肿瘤细胞在应激下生存的适应性机制。