小细胞肺癌的分子亚型、预测标志物和预后。

IF 2.5 4区 医学 Q2 PATHOLOGY
Yanli Zhu, Sheng Li, Haiyue Wang, Wenhao Ren, Kaiwen Chi, Jianghua Wu, Luning Mao, Xiaozheng Huang, Minglei Zhuo, Dongmei Lin
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引用次数: 0

摘要

目的:提出一种新的小细胞肺癌分子亚型分类方法。我们旨在使用免疫组织化学(IHC)进一步验证各种SCLC患者样本的分类,以强调其临床意义。方法:我们用IHC分析了195例SCLC患者的216份标本中四种亚型(阿切特-黄芩家族BHLH转录因子1(ASCL1)、神经元分化1(NEUROD1)、POU 2类同源盒3(POU2F3)和Yes1相关转录调节因子(YAP1))和两种预测标志物(德尔塔样配体3(DLL3)和MYC)的蛋白表达,包括21对切除的活检肿瘤。还探讨了分子亚型、临床病理特征和预后影响之间的关系。结果:ASCL1、NEUROD1、POU2F3、YAP1、DLL3和MYC的阳性表达率分别为70.3%、56.9%、14.9%、19.0%、75.4%和22.6%。DLL3的表达分别与ASCL1和POU2F3/YAP1的表达呈正相关和负相关,而MYC的表达则相反。ASCL1的强相关性(ρ=0.8603,P结论:我们的研究结果为SCLC分子亚型分类的诊断、预后和预测意义提供了临床见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular subtypes, predictive markers and prognosis in small-cell lung carcinoma.

Aims: A new molecular subtype classification was proposed for small-cell lung carcinoma (SCLC). We aimed to further validate the classification in various SCLC patient samples using immunohistochemistry (IHC) to highlight its clinical significance.

Methods: We analysed the protein expression of four subtype (achaete-scute family BHLH transcription factor 1 (ASCL1), neuronal differentiation 1 (NEUROD1), POU class 2 homeobox 3 (POU2F3) and Yes1-associated transcriptional regulator (YAP1)) and two predictive markers (delta-like ligand 3 (DLL3) and MYC) using IHC in 216 specimens from 195 SCLC patients, including 21 pairs of resected biopsy tumours. Associations among molecular subtypes, clinicopathological features and prognostic implications were also explored.

Results: The ASCL1, NEUROD1, POU2F3, YAP1, DLL3 and MYC-positive expression rates were 70.3%, 56.9%, 14.9%, 19.0%, 75.4% and 22.6%, respectively. DLL3 expression had positive and negative associations with that of ASCL1 and POU2F3/YAP1, respectively, whereas MYC had the opposite effect. Strong associations of ASCL1 (Ρ=0.8603, p<0.0001), NEUROD1 (Ρ=0.8326, p<0.0001), POU2F3 (Ρ=0.6950, p<0.0001) and YAP1 (Ρ=0.7466, p<0.0001) expressions were detected between paired resected biopsy tumours. In addition to SCLC-A (ASCL1-dominant), SCLC-N (NEUROD1-dominant) and SCLC-P (POU2F3-dominant), unsupervised hierarchical cluster analyses identified a fourth, quadruple-negative SCLC subtype (SCLC-QN) characterised by the low expression of all four subtype-specific proteins, and 55.4% (n=108), 27.2% (n=53), 11.8% (n=23) and 5.6% (n=11) were categorised as SCLC-A, SCLC-N, SCLC-P and SCLC-QN, respectively. Significant enrichment of SCLC-P in the combined SCLC cohort was observed, and adenocarcinoma was more prevalent in SCLC-A, while large-cell neuroendocrine carcinoma was more commonly seen in SCLC-P. No survival difference was found among molecular subtypes.

Conclusions: Our results provide clinical insights into the diagnostic, prognostic and predictive significance of SCLC molecular subtype classifications.

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来源期刊
CiteScore
7.80
自引率
2.90%
发文量
113
审稿时长
3-8 weeks
期刊介绍: Journal of Clinical Pathology is a leading international journal covering all aspects of pathology. Diagnostic and research areas covered include histopathology, virology, haematology, microbiology, cytopathology, chemical pathology, molecular pathology, forensic pathology, dermatopathology, neuropathology and immunopathology. Each issue contains Reviews, Original articles, Short reports, Correspondence and more.
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