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厄洛替尼和卡博替尼对A549非小细胞肺癌的增强抗肿瘤作用:体内和体外研究

Augmented antitumor effects of erlotinib and cabozantinib on A549 non-small cell lung cancer: and studies.

作者信息

Alhazzani Khalid, Alsahli Meshal, Alanazi Ahmed Z, Algahtani Mohammad, Alenezi Ahmad A, Alhoshani Ali, Alqinyah Mohammed, Alhamed Abdullah S, Alhosaini Khaled

机构信息

Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.

出版信息

Saudi Pharm J. 2023 Oct;31(10):101756. doi: 10.1016/j.jsps.2023.101756. Epub 2023 Aug 24.

Abstract

Non-small cell lung carcinoma is a challenging disease worldwide. This study aims to determine whether combining erlotinib, an epidermal growth factor receptor (EGFR) inhibitor, with cabozantinib, a mesenchymal-epithelial transition factor (c-Met) inhibitor, would have an augmented therapeutic benefit on A549 cells. The combination of erlotinib and cabozantinib (5 µM) inhibited A549 cell viability compared to each monotherapy at ≥ 10 µM as confirmed by the MTT assay. Combination therapy also has a more potent inhibition of cellular migration than monotherapy using the wound-healing assay. Furthermore, mRNA expression analyses for assessing apoptosis, metastasis, and cell cycle-related genes, the results showed that combination therapy significantly inhibits levels of BCL-2, MMP-9, VEGF, and TGF-β while inducing p53, p21, and BAX expression. In terms of oncogenic markers, western blotting analysis showed a significant reduction of BCl-2 expression and elevation in caspase3, p53, and p21 proteins as indicators of cell death via apoptosis. The antitumor effect of the combination therapy showed significant tumor inhibition compared to monotherapy. In conclusion, combination therapy could be a potential promising strategy to treat non-small cell lung carcinoma.

摘要

非小细胞肺癌是一种在全球范围内颇具挑战性的疾病。本研究旨在确定表皮生长因子受体(EGFR)抑制剂厄洛替尼与间充质上皮转化因子(c-Met)抑制剂卡博替尼联合使用是否会对A549细胞产生增强的治疗效果。MTT分析证实,与每种单药治疗(≥10 µM)相比,厄洛替尼和卡博替尼(5 µM)联合使用可抑制A549细胞活力。使用伤口愈合试验,联合治疗对细胞迁移的抑制作用也比单药治疗更强。此外,通过对评估细胞凋亡、转移和细胞周期相关基因的mRNA表达分析,结果表明联合治疗可显著抑制BCL-2、MMP-9、VEGF和TGF-β的水平,同时诱导p53、p21和BAX的表达。在致癌标志物方面,蛋白质印迹分析显示,作为细胞凋亡导致细胞死亡的指标,BCl-2表达显著降低,caspase3、p53和p21蛋白水平升高。与单药治疗相比,联合治疗的抗肿瘤作用显示出显著的肿瘤抑制效果。总之,联合治疗可能是一种治疗非小细胞肺癌的潜在有前景的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c2c/10495648/c0520dcdc394/gr1.jpg

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