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骨肉瘤中铁死亡相关基因预测列线图的构建与验证

Construction and validation of a predictive nomogram for ferroptosis-related genes in osteosarcoma.

作者信息

Meng Jinzhi, Du Huawei, Lu Jinfeng, Wang Hongtao

机构信息

Bone and Joint Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.

Department of Pathology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.

出版信息

J Cancer Res Clin Oncol. 2023 Nov;149(15):14227-14239. doi: 10.1007/s00432-023-05225-9. Epub 2023 Aug 9.

Abstract

BACKGROUND

Ferroptosis is a new type of cellular regulation of necrosis that has attracted great attention in recent years, which is different from the traditional mode of autophagy, apoptosis, and necrosis. Studies suggest that ferroptosis is key to the occurrence and development of tumors.

METHODS

Here, we investigated the prognostic significance of ferroptosis-related genes (FRGs) in osteosarcoma (OS) using RNA transcriptome data from 88 OS samples collected from the UCSC Xena platform. We defined the OS sample from the UCSC platform as the training cohort and the GEO dataset (GSE21257 and GSE16091) as the validation cohorts. We assessed 73 up-regulated and 63 down-regulated FRGs. We divided patients from the UCSC database into groups at high risk and low risk and built a prognostic risk model to assess prognosis using five FRGs: MT1G, G6PD, ARNTL, BNIP3, and SQLE.

RESULTS

High-risk OS patients presented a lower survival rate. These results were confirmed in the validation groups. In the training group, the areas under the ROC curves (AUC) were as follows: 0.880 for 1 year, 0.833 for 3 years, and 0.818 for 5 years. In the GSE21257 validation cohort, the AUC were as follows: 0.770 for 1 year, 0.641 for 3 years, and 0.632 for 5 years survival, and in the GSE16091 were 0.729 for 1 year, 0.663 for 3 years, and 0.735 for 5 years survival.

CONCLUSIONS

These findings suggest that FRGs are associated with the prognosis of osteosarcoma. Moreover, our prognostic risk model can predict overall survival in osteosarcoma. This provides new ideas for the clinical diagnosis and personalized treatment of osteosarcoma.

摘要

背景

铁死亡是近年来备受关注的一种新型细胞坏死调控方式,与传统的自噬、凋亡和坏死模式不同。研究表明,铁死亡是肿瘤发生发展的关键。

方法

在此,我们使用从UCSC Xena平台收集的88例骨肉瘤(OS)样本的RNA转录组数据,研究了铁死亡相关基因(FRGs)在骨肉瘤中的预后意义。我们将来自UCSC平台的OS样本定义为训练队列,将GEO数据集(GSE21257和GSE16091)定义为验证队列。我们评估了73个上调的FRGs和63个下调的FRGs。我们将来自UCSC数据库的患者分为高风险组和低风险组,并使用五个FRGs(MT1G、G6PD、ARNTL、BNIP3和SQLE)构建了一个预后风险模型来评估预后。

结果

高风险骨肉瘤患者的生存率较低。这些结果在验证组中得到了证实。在训练组中,ROC曲线下面积(AUC)如下:1年时为0.880,3年时为0.833,5年时为0.818。在GSE21257验证队列中,1年生存率的AUC为0.770,3年生存率的AUC为0.641,5年生存率的AUC为0.632;在GSE16091中,1年生存率的AUC为0.729,3年生存率的AUC为0.663,5年生存率的AUC为0.735。

结论

这些发现表明FRGs与骨肉瘤的预后相关。此外,我们的预后风险模型可以预测骨肉瘤的总生存率。这为骨肉瘤的临床诊断和个性化治疗提供了新思路。

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