Department of Thoracic Surgery, Thoraxklinik, University Hospital Heidelberg, Heidelberg, Germany.
Translational Lung Research Centre Heidelberg (TLRC-H), German Centre for Lung Research (DZL), Heidelberg, Germany.
PLoS One. 2018 Oct 23;13(10):e0206132. doi: 10.1371/journal.pone.0206132. eCollection 2018.
The current classification of human lung adenocarcinoma defines five different histological growth patterns within the group of conventional invasive adenocarcinomas. The five growth patterns are characterised by their typical architecture, but also by variable tumor biological behaviour.
The aim of this study was to identify specific gene signatures of the five adenocarcinoma growth patterns defined by the joint IASLC/ATS/ERS working group.
Total RNA from microdissected adenocarcinoma tissue samples of ten lepidic, ten acinar, ten solid, nine papillary, and nine micropapillary tumor portions was isolated and prepared for gene expression analysis. Differential expression of genes was determined using the R package "LIMMA". The overall significance of each signature was assessed via global test. Gene ontology statistics were analysed using GOstat. For immunohistochemical validation, tissue specimens from 20 tumors with solid and 20 tumors with lepidic growth pattern were used.
Microarray analyses between the growth patterns resulted in numerous differentially expressed genes between the solid architecture and other patterns. The comparison of transcriptomic activity in the solid and lepidic patterns revealed 705 up- and 110 downregulated non-redundant genes. The pattern-specific protein expression of Inositol-1,4,5-trisphosphate-kinase-A (ITPKA) and angiogenin by immunohistochemistry confirmed the RNA levels. The strongest differences in protein expression between the two patterns were shown for ITPKA (p = 0.02) and angiogenin (p = 0.113).
In this study growth pattern-specific gene signatures in pulmonary adenocarcinoma were identified and distinct transcriptomic differences between lung adenocarcinoma growth patterns were defined. The study provides valuable new information about pulmonary adenocarcinoma and allows a better assessment of the five adenocarcinoma subgroups.
当前的人类肺腺癌分类在传统浸润性腺癌组中定义了五种不同的组织学生长模式。这五种生长模式的特点是其典型的结构,但也具有可变的肿瘤生物学行为。
本研究旨在确定由国际肺癌研究协会/美国胸科学会/欧洲呼吸学会工作组联合定义的五种腺癌生长模式的特定基因特征。
从十个贴壁型、十个腺泡型、十个实体型、九个乳头型和九个微乳头型肿瘤部分的微切割腺癌组织样本中分离并制备总 RNA 进行基因表达分析。使用 R 包“LIMMA”确定基因的差异表达。通过全局检验评估每个签名的整体显著性。使用 GOstat 分析基因本体统计学。为了进行免疫组织化学验证,使用 20 个具有实体生长模式和 20 个具有贴壁生长模式的肿瘤组织标本。
生长模式之间的微阵列分析导致实体结构与其他模式之间存在许多差异表达的基因。实体和贴壁模式转录组活性的比较显示出 705 个上调和 110 个下调的非冗余基因。免疫组织化学证实了肌醇-1,4,5-三磷酸激酶-A(ITPKA)和血管生成素的模式特异性蛋白表达。两种模式之间蛋白表达的最强差异为 ITPKA(p = 0.02)和血管生成素(p = 0.113)。
在这项研究中,确定了肺腺癌中具有生长模式特异性的基因特征,并定义了肺腺癌生长模式之间明显的转录组差异。该研究提供了有关肺腺癌的宝贵新信息,并允许更好地评估五个腺癌亚组。