转录因子 SALL4 和 OCT4 在非小细胞肺癌 (NSCLC) 中的表达。

Translational respiratory medicine Pub Date : 2014-10-02 eCollection Date: 2014-12-01 DOI:10.1186/s40247-014-0010-7
Erika Rodriguez, Li Chen, Ming-Hui Ao, Susan Geddes, Ed Gabrielson, Frederic Askin, Hui Zhang, Qing Kay Li
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引用次数: 0

摘要

背景:SALL4和OCT4是转录因子,在干细胞发育和肿瘤发生过程中发挥着重要作用。然而,这些转录因子在肺癌中的表达还没有得到很好的研究。在这项研究中,我们通过免疫化学方法评估了SALL4和OCT4在非小细胞肺癌(NSCLC)中的表达。我们用 77 个原发性肺腺癌(ADC)和 90 个原发性肺鳞状细胞癌(SqCC)构建了 NSCLC 组织芯片(TMA)。使用小鼠单克隆抗人 SALL4(1:400 稀释度)和多克隆抗人 OCT4(1:200 稀释度)抗体。SALL4 和 OCT4 的核染色采用三级评分法进行半定量评分。SALL4和OCT4的表达与肿瘤分化、病理分期和患者的临床信息相关:结果:在原发性 ADC 中,SALL4 和 OCT4 的强表达率分别为 7.8%和 9.1%。SALL4的强表达与肿瘤分化呈反比。在原发性SqCC中,SALL4和OCT4的强表达率分别为16.7%和0%。SALL4的表达与OCT4的表达相关,但与SqCCs的肿瘤分期成反比:我们发现,SALL4和OCT4在原发性ADC和SqCC中均有不同程度的表达。我们的发现表明,不同的干细胞标志物可能在不同亚型的NSCLC中表达和/或发挥不同的作用。SALL4和OCT4在NSCLC中的潜在作用有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Expression of transcript factors SALL4 and OCT4 in a subset of non-small cell lung carcinomas (NSCLC).

Expression of transcript factors SALL4 and OCT4 in a subset of non-small cell lung carcinomas (NSCLC).

Expression of transcript factors SALL4 and OCT4 in a subset of non-small cell lung carcinomas (NSCLC).

Expression of transcript factors SALL4 and OCT4 in a subset of non-small cell lung carcinomas (NSCLC).

Background: SALL4 and OCT4 are transcription factors and play essential roles in stem cell development and oncogenesis. However, the expression of these transcription factors has not been well studied in lung cancers. In this study, we evaluated the expression of SALL4 and OCT4 in non-small cell lung carcinomas (NSCLC) by immunochemistry. NSCLC tissue microarrays (TMAs) were constructed with a total of 77 primary lung adenocarcinomas (ADCs) and 90 primary lung squamous cell carcinomas (SqCCs). A mouse monoclonal anti-human SALL4 (1:400 dilution) and a polyclonal anti-human OCT4 (1:200 dilution) antibodies were used. Nuclear staining of SALL4 and OCT4 was scored semi-quantitatively using a three tiered scale. The expressions of SALL4 and OCT4 were correlated with the tumor differentiation, pathological stage, and patients' clinical information.

Results: In primary ADCs, the stronger expression of SALL4 and OCT4 was 7.8% and 9.1%, respectively. The stronger expression of SALL4 was inversely correlated with tumor differentiations. In primary SqCCs, the stronger expressions of SALL4 and OCT4 were 16.7% and 0%, respectively. The expression of SALL4 is correlated with the expression of OCT4, but inversely correlated with the tumor stage in SqCCs.

Conclusions: We found that both SALL4 and OCT4 were differentially expressed in a subset of primary ADC and SqCC. Our finding suggest that different stem cell markers may be expressed and/or play differential role in different subtypes of NSCLC. The potential role of SALL4 and OCT4 needs to be further investigated in NSCLC.

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