CircPTP4A2 (hsa_circ_0007364) facilitates non-small cell lung cancer progression by regulating miR-127-5p/SMC3.

IF 4.9 2区 生物学 Q1 BIOLOGY
Yali Feng, Jiang Hong, Changgang Yang, Chun Cheng, Yujie Xue, Jiaqi Zhang, Yu Lu, Xiang Cao, Gengxi Jiang, Xiaodan Chong
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Abstract

Non-small cell lung cancer (NSCLC) is a major subtype of lung cancer and accounts for a large proportion of cancer-related deaths worldwide. Despite extensive research progress in recent years, the diagnosis and treatment of lung cancer remain insufficient. There is an urgent need to deepen the mechanistic understanding of lung cancer, develop early diagnostic strategies, and explore novel therapeutic targets. In this study, qRT-PCR was used to detect the expression of circPTP4A2 (circular RNA PTP4A2) in tumor and adjacent normal tissues from 50 NSCLC patients. CircPTP4A2 was significantly upregulated in tumor tissues and was closely associated with patient survival and prognosis. In vitro silencing of circPTP4A2 in NSCLC cell lines SPCA1 and H1299 significantly inhibited cell proliferation and malignant metastatic potential. Moreover, modulating the expression of miR-127-5p and SMC3 effectively reversed the phenotypic changes induced by circPTP4A2 knockdown. In conclusion, circPTP4A2 is upregulated in NSCLC and promotes tumorigenesis and progression through the miR-127-5p/SMC3 signaling axis.

CircPTP4A2 (hsa_circ_0007364)通过调节miR-127-5p/SMC3促进非小细胞肺癌的进展。
非小细胞肺癌(NSCLC)是肺癌的主要亚型,在全球癌症相关死亡中占很大比例。尽管近年来研究取得了广泛进展,但肺癌的诊断和治疗仍然不足。迫切需要加深对肺癌的机制认识,制定早期诊断策略,探索新的治疗靶点。本研究采用qRT-PCR检测了50例NSCLC患者肿瘤及邻近正常组织中circPTP4A2(环状RNA PTP4A2)的表达。CircPTP4A2在肿瘤组织中表达显著上调,与患者生存和预后密切相关。体外沉默非小细胞肺癌细胞系SPCA1和H1299中的circPTP4A2可显著抑制细胞增殖和恶性转移潜能。此外,调节miR-127-5p和SMC3的表达可有效逆转circPTP4A2敲低引起的表型变化。总之,circPTP4A2在NSCLC中表达上调,并通过miR-127-5p/SMC3信号轴促进肿瘤发生和进展。
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
Biology Direct
Biology Direct 生物-生物学
CiteScore
6.40
自引率
10.90%
发文量
32
审稿时长
7 months
期刊介绍: Biology Direct serves the life science research community as an open access, peer-reviewed online journal, providing authors and readers with an alternative to the traditional model of peer review. Biology Direct considers original research articles, hypotheses, comments, discovery notes and reviews in subject areas currently identified as those most conducive to the open review approach, primarily those with a significant non-experimental component.
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