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表皮生长因子受体(EGFR)突变型腺癌中的假小细胞转化

Pseudo-small cell transformation in EGFR-mutant adenocarcinoma.

作者信息

Li Rui, Jiang Lili, Zhou Xiaojuan, Lu You, Zhang Yan

机构信息

Department of Thoracic Oncology, Cancer Center, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

Department of Pathology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

出版信息

Lung Cancer. 2021 Mar;153:120-125. doi: 10.1016/j.lungcan.2020.12.036. Epub 2021 Jan 10.

Abstract

OBJECTIVES

To investigate the phenomenon of pseudo-small cell transformation (SCT) by reviewing SCT cases from the past 2 years.

MATERIALS & METHODS: A total of 11 cases with reported SCT cases from 7282 lung cancer cases treated in West China Hospital of Sichuan University were identified between January 2017 and March 2018. All initial lung adenocarcinoma pathological slides of SCT patients were reviewed carefully by independent, blinded pathologists. Immunohistochemistry was used to identify the expression of EGFR, RB1 and TP53.

RESULTS

Surprisingly, 8 of 11 previously SCT samples actually contained variable, but discernible amounts of SCLC components, varying from less than 1%-5%. Dubious small-cell components were found in two other patients. Only one patient's sample had no SCLC component on previous adenocarcinoma sections and was therefore defined as a real SCT case. In the current study, we found that at least 72.7 % (8/11) of SCT cases were actually pseudo-SCT. The immunohistochemistry results showed that the EGFR protein was only expressed in the adenocarcinoma component, but not in the SCLC component, indicating that they may not originate from identical cell clones. RB1 deletion and mutated TP53 overexpression were observed in either pseudo-SCT or real SCT.

CONCLUSIONS

Our findings indicated that most SCT may be pseudo-SCT in real world. Pseudo-SCT may lead to bias conclusion from previous researches about SCT. The real mechanism of SCT deserves further investigation.

摘要

目的

通过回顾过去2年的小细胞转化(SCT)病例,研究假性小细胞转化现象。

材料与方法

在2017年1月至2018年3月期间,从四川大学华西医院治疗的7282例肺癌病例中,共确定了11例报告有SCT病例。所有SCT患者的初始肺腺癌病理切片均由独立的、不知情的病理学家仔细复查。采用免疫组织化学法检测EGFR、RB1和TP53的表达。

结果

令人惊讶的是,11例先前诊断为SCT的样本中,有8例实际上含有数量不等但可辨别的小细胞肺癌成分,比例从不到1%至5%不等。另外两名患者中发现了可疑的小细胞成分。只有一名患者的样本在先前的腺癌切片中没有小细胞肺癌成分,因此被定义为真正的SCT病例。在本研究中,我们发现至少72.7%(8/11)的SCT病例实际上是假性SCT。免疫组织化学结果显示,EGFR蛋白仅在腺癌成分中表达,而不在小细胞肺癌成分中表达,这表明它们可能并非源自相同的细胞克隆。在假性SCT或真正的SCT中均观察到RB1缺失和TP53突变过表达。

结论

我们的研究结果表明,在现实世界中,大多数SCT可能是假性SCT。假性SCT可能导致先前关于SCT的研究得出有偏差的结论。SCT的真正机制值得进一步研究。

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