{"title":"电化学性能增强的聚合物复合材料及其在非小细胞肺癌治疗中的应用","authors":"Yujun Wei , Zhiling Zhang , Tianrang Ao","doi":"10.1016/j.molstruc.2025.141813","DOIUrl":null,"url":null,"abstract":"<div><div>Cancer, particularly non-small cell lung cancer (NSCLC), remains a leading cause of cancer-related deaths, with a dismal 5-year survival rate of approximately 15 %. This underscores the urgent need for novel, safe, and effective targeted therapies. In this study, we synthesized compound 1 for lung cancer treatment, considering the challenges in drug delivery. A new three-dimensional (3D) La(III)-based coordination polymer with the chemical composition of {[La(L)(H<sub>2</sub>O)<sub>3</sub>]Cl·H<sub>2</sub>O}<sub>n</sub> (<strong>1</strong>) (H<sub>2</sub>L = (4-(pyridyl-N-oxide)methylphosphonic acid), was successfully self-assembled via diffusion method at room temperature and characterized by single-crystal X-ray diffraction, elemental analyses and FT-IR. Following this, we developed a composite drug delivery material, PCL-CB@CP1@1, and assessed its inhibitory effects on NSCLC cell proliferation. The results demonstrated that PCL-CB@CP1@1 effectively inhibited cell growth by modulating the Nrf2/HO-1/GPX4 signaling pathway. Additionally, molecular docking simulations indicated multiple binding interactions between the La(III) complex and receptor sites, further highlighting its significant biological activity. These findings suggest that PCL-CB@CP1@1 holds potential as a targeted therapeutic agent for lung cancer treatment, offering new possibilities for improving patient outcomes.</div></div>","PeriodicalId":16414,"journal":{"name":"Journal of Molecular Structure","volume":"1334 ","pages":"Article 141813"},"PeriodicalIF":4.9000,"publicationDate":"2025-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Polymer composites with enhanced electrochemical properties and their application in non-small cell lung cancer treatment\",\"authors\":\"Yujun Wei , Zhiling Zhang , Tianrang Ao\",\"doi\":\"10.1016/j.molstruc.2025.141813\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Cancer, particularly non-small cell lung cancer (NSCLC), remains a leading cause of cancer-related deaths, with a dismal 5-year survival rate of approximately 15 %. This underscores the urgent need for novel, safe, and effective targeted therapies. In this study, we synthesized compound 1 for lung cancer treatment, considering the challenges in drug delivery. A new three-dimensional (3D) La(III)-based coordination polymer with the chemical composition of {[La(L)(H<sub>2</sub>O)<sub>3</sub>]Cl·H<sub>2</sub>O}<sub>n</sub> (<strong>1</strong>) (H<sub>2</sub>L = (4-(pyridyl-N-oxide)methylphosphonic acid), was successfully self-assembled via diffusion method at room temperature and characterized by single-crystal X-ray diffraction, elemental analyses and FT-IR. Following this, we developed a composite drug delivery material, PCL-CB@CP1@1, and assessed its inhibitory effects on NSCLC cell proliferation. The results demonstrated that PCL-CB@CP1@1 effectively inhibited cell growth by modulating the Nrf2/HO-1/GPX4 signaling pathway. Additionally, molecular docking simulations indicated multiple binding interactions between the La(III) complex and receptor sites, further highlighting its significant biological activity. These findings suggest that PCL-CB@CP1@1 holds potential as a targeted therapeutic agent for lung cancer treatment, offering new possibilities for improving patient outcomes.</div></div>\",\"PeriodicalId\":16414,\"journal\":{\"name\":\"Journal of Molecular Structure\",\"volume\":\"1334 \",\"pages\":\"Article 141813\"},\"PeriodicalIF\":4.9000,\"publicationDate\":\"2025-07-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Molecular Structure\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0022286025004995\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/2/21 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Structure","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022286025004995","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/21 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
癌症,特别是非小细胞肺癌(NSCLC),仍然是癌症相关死亡的主要原因,其5年生存率约为15%。这凸显了对新型、安全、有效的靶向治疗的迫切需求。在本研究中,考虑到药物传递方面的挑战,我们合成了用于肺癌治疗的化合物1。采用扩散法制备了一种新的三维(3D) La(III)基配位聚合物,化学成分为{[La(L)(H2O)3]Cl·H2O}n (1) (H2L =(4-(吡啶基- n -氧化物)甲基膦酸),并通过单晶x射线衍射、元素分析和红外光谱对其进行了表征。在此之后,我们开发了一种复合给药材料PCL-CB@CP1@1,并评估了其对NSCLC细胞增殖的抑制作用。结果表明PCL-CB@CP1@1通过调控Nrf2/HO-1/GPX4信号通路有效抑制细胞生长。此外,分子对接模拟表明La(III)复合物与受体位点之间存在多种结合相互作用,进一步突出了其重要的生物活性。这些发现表明PCL-CB@CP1@1具有作为肺癌治疗的靶向治疗剂的潜力,为改善患者预后提供了新的可能性。
Polymer composites with enhanced electrochemical properties and their application in non-small cell lung cancer treatment
Cancer, particularly non-small cell lung cancer (NSCLC), remains a leading cause of cancer-related deaths, with a dismal 5-year survival rate of approximately 15 %. This underscores the urgent need for novel, safe, and effective targeted therapies. In this study, we synthesized compound 1 for lung cancer treatment, considering the challenges in drug delivery. A new three-dimensional (3D) La(III)-based coordination polymer with the chemical composition of {[La(L)(H2O)3]Cl·H2O}n (1) (H2L = (4-(pyridyl-N-oxide)methylphosphonic acid), was successfully self-assembled via diffusion method at room temperature and characterized by single-crystal X-ray diffraction, elemental analyses and FT-IR. Following this, we developed a composite drug delivery material, PCL-CB@CP1@1, and assessed its inhibitory effects on NSCLC cell proliferation. The results demonstrated that PCL-CB@CP1@1 effectively inhibited cell growth by modulating the Nrf2/HO-1/GPX4 signaling pathway. Additionally, molecular docking simulations indicated multiple binding interactions between the La(III) complex and receptor sites, further highlighting its significant biological activity. These findings suggest that PCL-CB@CP1@1 holds potential as a targeted therapeutic agent for lung cancer treatment, offering new possibilities for improving patient outcomes.
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