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尼氯硝唑通过抑制肺耐药相关蛋白和 c-myc 增强顺铂耐药人肺癌细胞中顺铂的细胞毒性作用。

Niclosamide enhances the cytotoxic effect of cisplatin in cisplatin-resistant human lung cancer cells via suppression of lung resistance-related protein and c-myc.

机构信息

Cancer Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong 524000, P.R. China.

出版信息

Mol Med Rep. 2018 Mar;17(3):3497-3502. doi: 10.3892/mmr.2017.8301. Epub 2017 Dec 18.

DOI:10.3892/mmr.2017.8301
PMID:29257330
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5802146/
Abstract

Lung cancer is a leading cause of cancer-associated mortality worldwide. The cisplatin (DDP)‑based chemotherapy remains the foundation of treatment for the majority of patients affected by advanced non‑small cell lung cancer (NSCLC). However, DDP‑resistance limits the clinical utility of this drug in patients with advanced NSCLC. The aim of the present study was to investigate the inhibitory effect of niclosamide on human lung cancer cell growth and to investigate the possible underlying mechanism. The effects of niclosamide on the proliferation of human lung adenocarcinoma (A549) and DDP‑resistant (CR) human lung adenocarcinoma (A549/DDP) cells were examined by Cell Counting kit‑8 assay. The impact of niclosamide on the apoptosis of A549/DDP cells was detected by Annexin V‑fluorescein isothiocyanate/propidium iodide assay. The expression levels of cisplatin‑resistant‑associated molecules (lung resistance‑related protein and c‑myc) following niclosamide treatment in A549/DDP cells were evaluated by western blot analysis. The results indicated that niclosamide in combination with DDP demonstrated a synergistic effect in A549/DDP cells and directly induced apoptosis, which may be associated with caspase‑3 activation. Furthermore, niclosamide decreased the expression level of c‑myc protein, which may influence DDP sensitivity of A549/DDP cells. Thus, the present study indicates that niclosamide combined with DDP exerts a synergistic effect in cisplatin‑resistant lung cancer cells and may present as a promising drug candidate in lung cancer therapy.

摘要

肺癌是全球癌症相关死亡的主要原因。顺铂(DDP)为基础的化疗仍然是大多数晚期非小细胞肺癌(NSCLC)患者的治疗基础。然而,DDP 耐药限制了该药物在晚期 NSCLC 患者中的临床应用。本研究旨在探讨尼氯硝唑对人肺癌细胞生长的抑制作用,并探讨其可能的潜在机制。通过 Cell Counting kit-8 检测试剂盒检测尼氯硝唑对人肺腺癌细胞(A549)和 DDP 耐药(CR)人肺腺癌细胞(A549/DDP)增殖的影响。通过 Annexin V-荧光素异硫氰酸酯/碘化丙啶检测试剂盒检测尼氯硝唑对 A549/DDP 细胞凋亡的影响。通过 Western blot 分析评估尼氯硝唑处理后 A549/DDP 细胞中顺铂耐药相关分子(肺耐药相关蛋白和 c-myc)的表达水平。结果表明,尼氯硝唑联合 DDP 在 A549/DDP 细胞中表现出协同作用,并直接诱导细胞凋亡,这可能与 caspase-3 的激活有关。此外,尼氯硝唑降低了 c-myc 蛋白的表达水平,这可能影响 A549/DDP 细胞对 DDP 的敏感性。因此,本研究表明,尼氯硝唑联合 DDP 对顺铂耐药的肺癌细胞具有协同作用,可能成为肺癌治疗的一种有前途的药物候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddba/5802146/94cde1dfe7f4/MMR-17-03-3497-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddba/5802146/a10bb378208a/MMR-17-03-3497-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddba/5802146/09147fa7d75c/MMR-17-03-3497-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddba/5802146/18adb2b7cf09/MMR-17-03-3497-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddba/5802146/4bdb1eb212a6/MMR-17-03-3497-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddba/5802146/018c82cdfe72/MMR-17-03-3497-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddba/5802146/94cde1dfe7f4/MMR-17-03-3497-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddba/5802146/a10bb378208a/MMR-17-03-3497-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddba/5802146/09147fa7d75c/MMR-17-03-3497-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddba/5802146/18adb2b7cf09/MMR-17-03-3497-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddba/5802146/4bdb1eb212a6/MMR-17-03-3497-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddba/5802146/018c82cdfe72/MMR-17-03-3497-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddba/5802146/94cde1dfe7f4/MMR-17-03-3497-g05.jpg

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