Department of Radiation Oncology, The First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.
Department of Head and Neck Surgery Section II, The Third Affiliated Hospital of Kunming Medical University (Tumor Hospital of Yunnan Province), Kunming, Yunnan, China.
Bioengineered. 2022 Mar;13(3):5190-5204. doi: 10.1080/21655979.2022.2037368.
Lung cancer is a significant global burden. Aminoacyl-tRNA synthetases (aaRSs) can be reliably identified by the occurrence and improvement of tumors. Threonyl-tRNA synthetase (TARS) and mitochondrial threonyl-tRNA synthetase 2 (TARS2) are both aaRSs. Many studies have shown that TARS are involved in tumor angiogenesis and metastasis. However, TARS2 has not yet been reported in tumors. This study explored the role of TARS2 in the proliferation and apoptosis of lung adenocarcinoma (LUAD). TARS2 expression in lung adenocarcinoma and non-cancerous lung tissues was detected via immunohistochemistry. Cell proliferation was detected using MTS, clone formation, and EdU staining assays. Flow cytometry was used to detect cell cycle, mitochondria reactive oxygen species (mROS) production, and apoptosis. Mitochondrial membrane potential (MMP ΔΨm) was detected using JC-1 fluorescent probes. Cell cycle, apoptosis-related pathway, and mitochondrial DNA (mtDNA) -encoded protein expression was detected via Western blotting. Finally, the effect of TARS2 on tumor growth was examined using a xenotransplanted tumor model in nude mice. We found that TARS2 was highly expressed in lung adenocarcinoma tissues and associated with poor overall survival (OS). Mechanistic analysis showed that knockdown of TARS2 inhibited proliferation through the retinoblastoma protein (RB) pathway and promoted mROS-induced apoptosis. Knockdown of TARS2 inhibits tumor growth in a xenotransplanted tumor model. TARS2 plays an important role in LUAD cell proliferation and apoptosis and may be a new therapeutic target.
肺癌是一个重大的全球负担。氨酰-tRNA 合成酶(aaRS)可以通过肿瘤的发生和改善来可靠地识别。苏氨酰-tRNA 合成酶(TARS)和线粒体苏氨酰-tRNA 合成酶 2(TARS2)都是 aaRS。许多研究表明,TARS 参与肿瘤血管生成和转移。然而,TARS2 在肿瘤中尚未被报道。本研究探讨了 TARS2 在肺腺癌(LUAD)增殖和凋亡中的作用。通过免疫组织化学检测肺腺癌和非癌性肺组织中的 TARS2 表达。使用 MTS、克隆形成和 EdU 染色检测细胞增殖。通过流式细胞术检测细胞周期、线粒体活性氧(mROS)产生和细胞凋亡。使用 JC-1 荧光探针检测线粒体膜电位(MMP ΔΨm)。通过 Western blot 检测细胞周期、凋亡相关通路和线粒体 DNA(mtDNA)编码蛋白的表达。最后,通过裸鼠异种移植肿瘤模型检测 TARS2 对肿瘤生长的影响。我们发现 TARS2 在肺腺癌组织中高表达,并与整体生存(OS)不良相关。机制分析表明,TARS2 敲低通过视网膜母细胞瘤蛋白(RB)通路抑制增殖,并促进 mROS 诱导的凋亡。TARS2 敲低抑制异种移植肿瘤模型中的肿瘤生长。TARS2 在 LUAD 细胞增殖和凋亡中起重要作用,可能是一个新的治疗靶点。