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RIOK1与非小细胞肺癌的临床特征相关,并促进癌症进展。

RIOK1 is associated with non-small cell lung cancer clinical characters and contributes to cancer progression.

作者信息

Wang Rong, Chai Wen-Shu, Pan Dian-Zhu, Shan Li-Na, Shi Xuan, He Yu-Hai, Pan Shuang

机构信息

Department of Respiratory, The First Affiliated Hospital Of Jinzhou Medical University, Jinzhou, Liaoning, 121001, China.

Department of Gastroenterology, The First Affiliated Hospital Of Jinzhou Medical University, Jinzhou, Liaoning, 121001, China.

出版信息

J Cancer. 2022 Jan 31;13(4):1289-1298. doi: 10.7150/jca.64668. eCollection 2022.

Abstract

Lung cancer is one of the most common malignant tumors and is currently the leading cause of cancer-related deaths worldwide. Although the treatment strategy has been significantly improved, the prognosis of lung cancer patients is still quite poor. RIOK1 has been reported to be highly expressed in non-small cell lung cancer (NSCLC), however, its clinical significance and biological function are still largely unknown in lung cancer. Using western blot and immunohistochemistry, we showed that RIOK1 was highly expressed in NSCLC tissues and correlated with advanced stage and poor prognosis. Furthermore, knockdown of RIOK1 could inhibit proliferation, migration, and invasion in NSCLC cells and tumorigenesis through AKT, Cyclin B1, MMP2, and EMT pathway. Furthermore, cell viability and apoptosis assays demonstrated that RIOK1 maintained NSCLC cell survival and reduced apoptosis rate when cells were treated with cisplatin. Western blot analysis demonstrated that RIOK1 depletion caused up-regulated protein expression of cleaved PARP and Caspase-3 in NSCLC cells. These findings revealed a novel function of RIOK1 in non-small cell lung cancer progression and suggest that RIOK1 might become a promising diagnostic and therapeutic target for this disease.

摘要

肺癌是最常见的恶性肿瘤之一,目前是全球癌症相关死亡的主要原因。尽管治疗策略已显著改善,但肺癌患者的预后仍然很差。据报道,RIOK1在非小细胞肺癌(NSCLC)中高表达,然而,其在肺癌中的临床意义和生物学功能仍 largely unknown。通过蛋白质免疫印迹法和免疫组织化学法,我们发现RIOK1在NSCLC组织中高表达,且与晚期和预后不良相关。此外,敲低RIOK1可通过AKT、细胞周期蛋白B1、基质金属蛋白酶2和上皮-间质转化(EMT)途径抑制NSCLC细胞的增殖、迁移和侵袭以及肿瘤发生。此外,细胞活力和凋亡检测表明,当用顺铂处理细胞时,RIOK1可维持NSCLC细胞存活并降低凋亡率。蛋白质免疫印迹分析表明,RIOK1缺失导致NSCLC细胞中裂解的聚(ADP-核糖)聚合酶(PARP)和半胱天冬酶-3的蛋白表达上调。这些发现揭示了RIOK1在非小细胞肺癌进展中的新功能,并表明RIOK1可能成为这种疾病有前景的诊断和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6f/8899362/06434095679b/jcav13p1289g001.jpg

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