Circ-PGAM1 Enhances Matrine Resistance of Non-Small Cell Lung Cancer via the miR-326/CXCR5 Axis.

IF 2.4 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Cancer Biotherapy and Radiopharmaceuticals Pub Date : 2024-10-01 Epub Date: 2022-12-21 DOI:10.1089/cbr.2022.0039
Caijun Dong, Liangwei Yang, Guofang Zhao
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引用次数: 0

Abstract

Background: Circular RNAs (circ-RNAs) have been demonstrated to influence initiation, drug resistance, and metastasis of tumors. However, the effects of circular-phosphoglycerate mutase 1 (circ-PGAM1) on matrine resistance in nonsmall cell lung cancer (NSCLC) remain unknown. Materials and Methods: The reverse transcription-quantitative polymerase chain reaction (RT-qPCR) was used to determine gene expression. The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) and cell colony formation assays were used to evaluate NSCLC apoptosis and cell proliferation after indicated treatments, respectively. Results: circ-PGAM1 was upregulated in human NSCLC cell lines (H1299 and A549) compared with the human normal lung epithelial (BEAS-2B) cells. circ-PGAM1 overexpression reversed the matrine treatment-induced inhibition on proliferation of NSCLC cells (A549 and H1299) and rescued the matrine treatment-stimulated apoptosis of these cells. miR-326 was demonstrated to interact with circ-PGAM1. circ-PGAM1 knockdown enhanced the antitumor effect of matrine on NSCLC cell proliferation and apoptosis, which was reversed by miR-326 inhibition. The authors also identified CXCR5 as a key downstream target of miR-326 in A549 cells. Conclusions: circ-PGAM1 enhances matrine resistance of NSCLC cells through the miR-326/CXCR5 axis. The authors' findings provide new insights into NSCLC-targeted therapy.

Circ-PGAM1 通过 miR-326/CXCR5 轴增强非小细胞肺癌的耐药性
背景:环状 RNA(circ-RNA)已被证实会影响肿瘤的发生、耐药性和转移。然而,环磷酸甘油酸突变酶 1(circ-PGAM1)对非小细胞肺癌(NSCLC)中马替林耐药性的影响仍然未知。材料与方法:采用反转录定量聚合酶链反应(RT-qPCR)测定基因表达。末端脱氧核苷酸转移酶 dUTP 缺口末端标记(TUNEL)和细胞集落形成试验分别用于评估经指定处理后的 NSCLC 细胞凋亡和细胞增殖情况。结果:与人类正常肺上皮细胞(BEAS-2B)相比,circ-PGAM1在人类NSCLC细胞系(H1299和A549)中上调。miR-326与circ-PGAM1相互作用,circ-PGAM1的敲除增强了matrine对NSCLC细胞增殖和凋亡的抗肿瘤作用,而miR-326的抑制则逆转了这种作用。作者还发现 CXCR5 是 miR-326 在 A549 细胞中的一个关键下游靶点。结论:circ-PGAM1通过miR-326/CXCR5轴增强了NSCLC细胞对matrine的耐药性。作者的发现为NSCLC靶向治疗提供了新的思路。
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来源期刊
CiteScore
7.80
自引率
2.90%
发文量
87
审稿时长
3 months
期刊介绍: Cancer Biotherapy and Radiopharmaceuticals is the established peer-reviewed journal, with over 25 years of cutting-edge content on innovative therapeutic investigations to ultimately improve cancer management. It is the only journal with the specific focus of cancer biotherapy and is inclusive of monoclonal antibodies, cytokine therapy, cancer gene therapy, cell-based therapies, and other forms of immunotherapies. The Journal includes extensive reporting on advancements in radioimmunotherapy, and the use of radiopharmaceuticals and radiolabeled peptides for the development of new cancer treatments.
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