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本文引用的文献

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Silencing of induces epithelial‑to‑mesenchymal transition in lung cancer cell lines with different effects on proliferation and clonogenic growth.[基因名称]的沉默在肺癌细胞系中诱导上皮-间质转化,对增殖和克隆生长有不同影响。 (注:原文中“Silencing of ”后面缺少具体基因名称,这里翻译时补充了“[基因名称]”)
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Analyses of rare predisposing variants of lung cancer in 6,004 whole genomes in Chinese.中国 6004 例全基因组中肺癌罕见易感变异体的分析。
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Expanding Horizons for Treatment of Early-Stage Lung Cancer.拓展早期肺癌治疗的视野
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Non-Small-Cell Lung Cancer in 2022: A Review for General Practitioners in Oncology.2022 年非小细胞肺癌:肿瘤学全科医生综述。
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Grainyhead-like (Grhl) Target Genes in Development and Cancer.粒头样 (Grhl) 靶基因在发育和癌症中的作用。
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Lung cancer.肺癌
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Update 2020: Management of Non-Small Cell Lung Cancer.更新于 2020 年:非小细胞肺癌的治疗。
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放疗和化疗后血液 GRHL2 对非小细胞肺癌患者的预后价值。

Prognostic value of blood GRHL2 in patients with non-small-cell lung cancer after radiotherapy and chemotherapy.

机构信息

Changzhou Cancer Hospital, Changzhou City, Jiangsu Province, 213000, P.R. China.

出版信息

Biomark Med. 2024;18(13-14):611-617. doi: 10.1080/17520363.2024.2366161. Epub 2024 Jul 29.

DOI:10.1080/17520363.2024.2366161
PMID:39073846
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11370899/
Abstract

We aimed to investigate the predictive value of the Grainyhead-like 2 (GRHL2) expression from circulating blood for recurrence, metastasis and overall death on patients with non-small-cell lung cancer (NSCLC). We collected blood samples from 122 patients who were admitted to our hospital for NSCLC. Multivariable Cox proportional-hazards analysis in adjusted Model II showed that compared with GRHL2-negative expression, positive expression in patients with NSCLC was associated with increased death risk (HR = 7.0, 95% CI: 2.1-20.9,  = 0.03) and risk for composite end point (HR = 8.2, 95% CI: 4.0-27.1, <0.01). This study supported that elevated circulating GRHL2 expression might be considered as a candidate prognostic biomarker for poor prognosis among these NSCLC patients.

摘要

我们旨在探讨来自循环血液的 Grainyhead-like 2 (GRHL2) 表达对非小细胞肺癌 (NSCLC) 患者复发、转移和总死亡的预测价值。我们收集了 122 名因 NSCLC 住院的患者的血液样本。调整后的模型 II 多变量 Cox 比例风险分析显示,与 GRHL2 阴性表达相比,NSCLC 患者的阳性表达与死亡风险增加(HR=7.0,95%CI:2.1-20.9,=0.03)和复合终点风险(HR=8.2,95%CI:4.0-27.1,<0.01)相关。这项研究支持循环 GRHL2 表达升高可能被认为是这些 NSCLC 患者预后不良的候选预后生物标志物。