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非靶向代谢组学和脂质组学鉴定出了小细胞肺癌的四种亚型。

Untargeted metabolomics and lipidomics identified four subtypes of small cell lung cancer.

作者信息

Zhang Chenyue, Shang Xiaoling, Wang Haiyong

机构信息

Department of Integrated Therapy, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.

Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.

出版信息

Metabolomics. 2022 Dec 27;19(1):3. doi: 10.1007/s11306-022-01964-x.

Abstract

INTRODUCTION

Small cell lung cancer (SCLC) is a heterogeneous malignancy with dismal prognosis. However, few studies have conducted on the metabolic heterogeneity in SCLC.

OBJECTIVE

We therefore identify SCLC classifications using untargeted metabolomics and lipidomics. We also compared their survival and the immunotherapy responses.

METHODS

Liquid Chromatography-Mass Spectrometry/Mass Spectrometry (LC-MS/MS) analysis was performed in 191 SCLC serum samples. Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis was conducted to identify metabolic pathways. The Kaplan-Meier and log-rank test were used to analyze the survival curves. The univariate and multivariate Cox proportional hazards regression models were used to evaluate prognostic factors for OS in patients with SCLC.

RESULTS

Distinct subtypes of SCLC were identified by consensus clustering algorithm using partioning around medoids (pam) based on untargeted metabolomics and lipidomics. Four distinct subtypes of SCLC were identified, with distinct metabolic pathways. Subgroup 2 had the longest survival whereas Subgroup 1 had the shortest. Subtype 2 benefited most from immunotherapy in OS, as in contrast to Subtype 3 with shortest survival.

CONCLUSION

Our study revealed the metabolic heterogeneity in SCLC and identified four subtypes with distinct metabolic features. It indicates promising therapeutic and prognostic value that may guide treatment for SCLC. The subtype-specific clinical trials may be designed and would be instructive for drug development.

摘要

引言

小细胞肺癌(SCLC)是一种异质性恶性肿瘤,预后较差。然而,针对SCLC代谢异质性的研究较少。

目的

因此,我们使用非靶向代谢组学和脂质组学来识别SCLC的分类。我们还比较了它们的生存率和免疫治疗反应。

方法

对191份SCLC血清样本进行液相色谱-质谱联用/质谱(LC-MS/MS)分析。进行京都基因与基因组百科全书(KEGG)分析以识别代谢途径。采用Kaplan-Meier法和对数秩检验分析生存曲线。使用单因素和多因素Cox比例风险回归模型评估SCLC患者总生存期的预后因素。

结果

基于非靶向代谢组学和脂质组学,通过使用围绕中心点划分(pam)的共识聚类算法识别出SCLC的不同亚型。识别出SCLC四个不同的亚型,具有不同的代谢途径。亚组2生存期最长,而亚组1生存期最短。在总生存期方面,亚型2从免疫治疗中获益最大,与之形成对比的是生存期最短的亚型3。

结论

我们的研究揭示了SCLC的代谢异质性,并识别出具有不同代谢特征的四个亚型。这表明其具有潜在的治疗和预后价值,可能为SCLC的治疗提供指导。可以设计亚型特异性临床试验,这对药物开发具有指导意义。

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