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Circulating tumor DNA and radiological tumor volume identify patients at risk for relapse with resected, early-stage non-small-cell lung cancer.循环肿瘤DNA和放射学肿瘤体积可识别接受手术切除的早期非小细胞肺癌患者的复发风险。
Ann Oncol. 2024 Feb;35(2):183-189. doi: 10.1016/j.annonc.2023.11.008. Epub 2023 Nov 21.
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Perioperative Durvalumab for Resectable Non-Small-Cell Lung Cancer.可切除非小细胞肺癌的围手术期度伐利尤单抗治疗。
N Engl J Med. 2023 Nov 2;389(18):1672-1684. doi: 10.1056/NEJMoa2304875. Epub 2023 Oct 23.
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Therapeutic Peptide RF16 Derived from CXCL8 Inhibits MDA-MB-231 Cell Invasion and Metastasis.来源于 CXCL8 的治疗性肽 RF16 抑制 MDA-MB-231 细胞侵袭和转移。
Int J Mol Sci. 2023 Sep 13;24(18):14029. doi: 10.3390/ijms241814029.
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Upregulated CXCL8 in placenta accreta spectruma regulates the migration and invasion of HTR-8/SVneo cells.胎盘植入谱中上调的 CXCL8 调节 HTR-8/SVneo 细胞的迁移和侵袭。
Mol Biol Rep. 2023 Oct;50(10):8189-8199. doi: 10.1007/s11033-023-08669-x. Epub 2023 Aug 10.
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First-line atezolizumab monotherapy versus single-agent chemotherapy in patients with non-small-cell lung cancer ineligible for treatment with a platinum-containing regimen (IPSOS): a phase 3, global, multicentre, open-label, randomised controlled study.一线阿特珠单抗单药治疗与含铂方案治疗不适用的非小细胞肺癌患者的单药化疗(IPSOS):一项全球、多中心、开放标签、随机对照的 3 期临床试验。
Lancet. 2023 Aug 5;402(10400):451-463. doi: 10.1016/S0140-6736(23)00774-2. Epub 2023 Jul 6.
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Perioperative Nivolumab and Chemotherapy in Stage III Non-Small-Cell Lung Cancer.III 期非小细胞肺癌的围手术期纳武利尤单抗和化疗。
N Engl J Med. 2023 Aug 10;389(6):504-513. doi: 10.1056/NEJMoa2215530. Epub 2023 Jun 28.
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CXCL8 blockade reduces fibrosis in endometriosis.CXCL8阻断可减轻子宫内膜异位症中的纤维化。
Nat Rev Immunol. 2023 Apr;23(4):203. doi: 10.1038/s41577-023-00861-1.
8
The Effect of on Non-Small-Cell Lung Cancer: A Research Based on Network and Experimental Pharmacology.基于网络和实验药理学的研究:探讨 对非小细胞肺癌的影响。
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9
Nitration of chemokine CXCL8 acts as a natural mechanism to limit acute inflammation.趋化因子 CXCL8 的硝化作用是作为一种天然机制来限制急性炎症。
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Comparison between Clinical Utility of CXCL-8 and Clinical Practice Tumor Markers for Colorectal Cancer Diagnosis.CXCL-8 与临床实践肿瘤标志物在结直肠癌诊断中的临床实用性比较。
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CXCL8在非小细胞肺癌患者中的表达及其与预后的关系。

Expression of CXCL8 and its relationship with prognosis in patients with non-small cell lung cancer.

作者信息

Ma Xuan, Zhu Xuean, Zou Mingli, Zhang Jingjing, Huang Lili, Jiang Shasha, Zhi Yanan

机构信息

Department of Respiratory Medicine, Suzhou BenQ Medical Center, The Affiliated BenQ Hospital of Nanjing Medical University Suzhou 215010, Jiangsu, China.

Department of General Surgery, Pingluo County People's Hospital Shizuishan 753000, Ningxia Hui Autonomous Region, China.

出版信息

Am J Cancer Res. 2024 Jun 15;14(6):2934-2945. doi: 10.62347/LJDQ3897. eCollection 2024.

DOI:10.62347/LJDQ3897
PMID:39005665
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11236764/
Abstract

To determine the expression of chemokine 8 (CXCL8) in non-small cell lung cancer (NSCLC) patients and analyze its correlation with tumor characteristics and patient prognosis. We conducted a retrospective analysis of 149 NSCLC patients treated between January 2016 and April 2018, measuring serum CXCL8 expression upon admission or prior to treatment. The clinical characteristics, including lymph node metastasis and staging, based on CXCL8 expression levels, were analyzed. Receiver Operating Characteristic (ROC) curves was drawn to assess its predictive value for lymph node metastasis and staging in NSCLC patients. Furthermore, the Kaplan-Meier curve was plotted to assess the impact of CXCL8 on 5-year survival in NSCLC Patients. NSCLC patients exhibited significantly higher serum CXCL8 levels than those with benign tumors (P<0.001), with the high CXCL8 expression group showing a higher incidence of lymph node metastasis or stage III NSCLC (P<0.01). CXCL8 was identified as an independent predictor of lymph node metastasis (AUC=0.730) and higher TNM stage (AUC=0.708), as well as a validated biomarker for predicting five-year survival in NSCLC patients. This study highlights the strong association between CXCL8 expression in NSCLC and patient prognosis, particularly regarding lymph node metastasis and clinical staging, suggesting the need for further research to explore CXCL8's specific role in the tumor microenvironment and its impact on different NSCLC subtypes.

摘要

为了确定趋化因子8(CXCL8)在非小细胞肺癌(NSCLC)患者中的表达,并分析其与肿瘤特征及患者预后的相关性。我们对2016年1月至2018年4月期间接受治疗的149例NSCLC患者进行了回顾性分析,测定入院时或治疗前血清CXCL8的表达水平。基于CXCL8表达水平分析包括淋巴结转移和分期在内的临床特征。绘制受试者工作特征(ROC)曲线以评估其对NSCLC患者淋巴结转移和分期的预测价值。此外,绘制Kaplan-Meier曲线以评估CXCL8对NSCLC患者5年生存率的影响。NSCLC患者血清CXCL8水平显著高于良性肿瘤患者(P<0.001),CXCL8高表达组淋巴结转移或III期NSCLC的发生率更高(P<0.01)。CXCL8被确定为淋巴结转移(AUC=0.730)和更高TNM分期(AUC=0.708)的独立预测因子,也是预测NSCLC患者5年生存率的有效生物标志物。本研究强调了NSCLC中CXCL8表达与患者预后之间的密切关联,特别是在淋巴结转移和临床分期方面,表明需要进一步研究以探索CXCL8在肿瘤微环境中的具体作用及其对不同NSCLC亚型的影响。