BACKGROUND: NUP155 was reported to involve breast invasive carcinoma and hepatocellular carcinoma. We hypothesized that NUP155 and NDC1impacted the progression of NSCLC. METHODS: The dataset was analyzed to find differentially expressed genes. Functional enrichment analysis and Kaplan-Meier survival analysis were performed for differentially expressed genes. Western blot, Clone formation assay, Transwell assay and CCK-8 assay were performed to determine the performance and role of the target gene in NSCLC. RESULTS: The research found that the NUP family played a role in various diseases. Differential expression analysis and survival analysis were performed to identify 6 related-genes, including NUP155, NDC1, KPNA2, MAD2L1, NUP62CL, and POM121L2NUP155 and NDC1 could interact with NUP53, respectively. This effect was necessary to complete the assembly of the nuclear pore complex. CONCLUSION: NUP155 interacted with NDC1 to complete the assembly of the nuclear pore complex, which promoted the development of NSCLC. Our study demonstrated that NUP155 was expected to be a potential target for the treatment of NSCLC.
NUP155 and NDC1 interaction in NSCLC: a promising target for tumor progression.
NUP155 和 NDC1 在非小细胞肺癌中的相互作用:肿瘤进展的一个有前景的靶点
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作者:Li Kai-Min, Meng Li-Fei, Yang Zhi-Hao, Hu Wen-Tao
| 期刊: | Frontiers in Pharmacology | 影响因子: | 4.800 |
| 时间: | 2024 | 起止号: | 2024 Dec 10; 15:1514367 |
| doi: | 10.3389/fphar.2024.1514367 | 研究方向: | 肿瘤 |
| 疾病类型: | 肺癌 | ||
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