Mitochondrial Ribosomal Protein L14 Promotes Cell Growth and Invasion by Modulating Reactive Oxygen Species in Thyroid Cancer.

IF 2.9 3区 医学 Q1 OTORHINOLARYNGOLOGY Clinical and Experimental Otorhinolaryngology Pub Date : 2023-05-01 DOI:10.21053/ceo.2022.01760
Hae Jong Kim, Quoc Khanh Nguyen, Seung-Nam Jung, Mi Ae Lim, Chan Oh, Yudan Piao, YanLi Jin, Ju-Hui Kim, Young Il Kim, Yea Eun Kang, Jae Won Chang, Ho-Ryun Won, Bon Seok Koo
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引用次数: 1

Abstract

Objectives: The mitochondrial ribosomal protein L14 (MRPL14) is encoded by a nuclear gene and participates in mitochondrial protein translation. In this study, we aimed to investigate the role of MRPL14 in thyroid cancer.

Methods: We investigated the association between MRPL14 expression and clinicopathological features using The Cancer Genome Atlas (TCGA) and Chungnam National University Hospital (CNUH) databases. Functional studies of MRPL14, including proliferation, migration, invasion, mitochondrial oxidative phosphorylation and reactive oxygen species (ROS) production, were performed in papillary thyroid cancer (PTC) cell lines (B-CPAP and KTC-1).

Results: Based on the TCGA dataset, PTC tissues lost mitochondrial integrity and showed dysregulated expression of overall mitoribosomal proteins (MRPs) compared with normal thyroid tissues. Of 78 MRPs, MRPL14 was highly expressed in thyroid cancer tissues. MRPL14 overexpression was significantly associated with advanced tumor stage, extrathyroidal extension, and lymph node metastasis. MRPL14 increased cell proliferation of thyroid cancer and promoted cell migration via epithelial-mesenchymal transition-related proteins. Moreover, MRPL14 knockdown reduced the expression of oxidative phosphorylation complex IV (MTCO1) and increased the accumulation of ROS. Cotreatment with a ROS scavenger restored cell proliferation and migration, which had been reduced by MRPL14 knockdown, implying that ROS functions as a key regulator of the oncogenic effects of MRPL14 in thyroid cancer cells.

Conclusion: Our findings indicate that MRPL14 may promote cell growth, migration, and invasion by modulating ROS in thyroid cancer cells.

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线粒体核糖体蛋白L14通过调节活性氧促进甲状腺癌细胞生长和侵袭。
目的:线粒体核糖体蛋白L14 (MRPL14)由核基因编码,参与线粒体蛋白翻译。在这项研究中,我们旨在探讨MRPL14在甲状腺癌中的作用。方法:利用癌症基因组图谱(TCGA)和忠南大学医院(CNUH)数据库研究MRPL14表达与临床病理特征之间的关系。在甲状腺乳头状癌(PTC)细胞系(B-CPAP和KTC-1)中进行了MRPL14的功能研究,包括增殖、迁移、侵袭、线粒体氧化磷酸化和活性氧(ROS)产生。结果:基于TCGA数据集,与正常甲状腺组织相比,PTC组织线粒体完整性丧失,总体线粒体糖蛋白(MRPs)表达失调。在78个MRPs中,MRPL14在甲状腺癌组织中高表达。MRPL14过表达与肿瘤分期、甲状腺外扩展和淋巴结转移显著相关。MRPL14增加甲状腺癌细胞增殖,并通过上皮-间质转化相关蛋白促进细胞迁移。此外,MRPL14敲低降低了氧化磷酸化复合物IV (MTCO1)的表达,增加了ROS的积累。与ROS清除剂共处理恢复了因MRPL14敲低而减少的细胞增殖和迁移,这表明ROS是MRPL14在甲状腺癌细胞中致癌作用的关键调节因子。结论:我们的研究结果表明,MRPL14可能通过调节甲状腺癌细胞中的ROS来促进细胞生长、迁移和侵袭。
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
CiteScore
4.90
自引率
6.70%
发文量
49
审稿时长
6-12 weeks
期刊介绍: Clinical and Experimental Otorhinolaryngology (Clin Exp Otorhinolaryngol, CEO) is an international peer-reviewed journal on recent developments in diagnosis and treatment of otorhinolaryngology-head and neck surgery and dedicated to the advancement of patient care in ear, nose, throat, head, and neck disorders. This journal publishes original articles relating to both clinical and basic researches, reviews, and clinical trials, encompassing the whole topics of otorhinolaryngology-head and neck surgery. CEO was first issued in 2008 and this journal is published in English four times (the last day of February, May, August, and November) per year by the Korean Society of Otorhinolaryngology-Head and Neck Surgery. The Journal aims at publishing evidence-based, scientifically written articles from different disciplines of otorhinolaryngology field. The readership contains clinical/basic research into current practice in otorhinolaryngology, audiology, speech pathology, head and neck oncology, plastic and reconstructive surgery. The readers are otolaryngologists, head and neck surgeons and oncologists, audiologists, and speech pathologists.
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