Inhibitory effects of icotinib combined with antiangiogenic drugs in human non‐small cell lung cancer xenograft models are better than single target drugs. Issue 2 (2nd December 2021)

• Record Type: Journal Article
• Authors: Jiang, Peng; Zhang, Yan; Cui, Jiadong; Wang, Xiuxiu; Li, Yu
• Is Part Of: Thoracic cancer. Volume 13:Issue 2(2022)
• Page Start: 257
• Page End: 264
• Publication Date: 2021-12-02
• Subjects: bevacizumab -- icotinib -- microvessel density -- recombinant human endostatin (rh‐endostatin) -- vascular endothelial growth factor A (VEGFA); Chest -- Cancer -- Periodicals; Chest -- Cancer -- Treatment -- Periodicals; Chest -- Surgery -- Periodicals; 616.99494005
• DOI: 10.1111/1759-7714.14261
• Languages: English
• ISSNs: 1759-7706

Abstract

Abstract: Background: This study aimed to evaluate the inhibitory effects and potential mechanisms of icotinib combined with antiangiogenic drugs on lung adenocarcinoma in vivo. Methods: A total of 72 mouse xenograft models established with human lung adenocarcinoma cells (HCC827) were randomly divided into six groups, including control, icotinib (Ic), bevacizumab (Bev), recombinant human endostatin (En), Ic + Bev and Ic + En groups. Mouse weights and tumor volumes were measured regularly. Half of the nude mice in each group were sacrificed after 16 days of drug treatment. The remaining animals were observed for another 16 days without drug supply. Immunohistochemical staining was performed to detect microvessel density in tumor heart, liver, brain specimens from the nude mice and Ki67 expression. Differential expression of vascular endothelial growth factor (VEGFA) in tumor tissue specimens was determined by ELISA and Western blot. Results: The results showed that the combined drugs inhibited tumor growth more substantially compared with single drugs, without increasing the toxic effects. The antiangiogenesis effect of the combination was better than that of single drug treatment. In addition, both types of targeted drugs and combination medication not only significantly reduced microvessel density in the tumor tissue itself, but also had a certain impact on decreasing microvessel density in the liver. The combination decreased VEGFA and Ki‐67 amounts significantly more than icotinib or endostatin as a monotherapy. Conclusions: Icotinib combined with bevacizumab or rh‐endostatin has a stronger inhibitory effect on tumor growth than single‐target drug in vivo, with no additional side effects. Abstract : We explored the inhibitory effects and its possible mechanisms of ecotinib combined with antiangiogenic drugs in human non‐small cell lung cancer xenograft models. The results confirmed that the combination therapy was more effective and had stronger inhibitory effects on the microvessel density of tumor tissues. After 16 days of drug withdrawal, the effects of antiangiogenic drugs on the body subsided.