INSERM U1256, NGERE-Nutrition, Genetics, and Environmental Risk Exposure, Faculty of Medicine of Nancy, University of Lorraine, 54000, Nancy, Vandoeuvre-lès-Nancy, France.
ENT Department, CHRU NANCY, 54511, Vandoeuvre-lès-Nancy, France.
Clin Epigenetics. 2021 Sep 25;13(1):179. doi: 10.1186/s13148-021-01122-5.
Nasal intestinal-type adenocarcinomas (ITAC) are strongly related to chronic wood dust exposure: The intestinal phenotype relies on CDX2 overexpression but underlying molecular mechanisms remain unknown. Our objectives were to investigate transcriptomic and methylation differences between healthy non-exposed and tumor olfactory cleft mucosae and to compare transcriptomic profiles between non-exposed, wood dust-exposed and ITAC mucosa cells.
We conducted a prospective monocentric study (NCT0281823) including 16 woodworkers with ITAC, 16 healthy exposed woodworkers and 13 healthy, non-exposed, controls. We compared tumor samples with healthy non-exposed samples, both in transcriptome and in methylome analyses. We also investigated wood dust-induced transcriptome modifications of exposed (without tumor) male woodworkers' samples and of contralateral sides of woodworkers with tumors. We conducted in parallel transcriptome and methylome analysis, and then, the transcriptome analysis was focused on the genes highlighted in methylome analysis. We replicated our results on dataset GSE17433.
Several clusters of genes enabled the distinction between healthy and ITAC samples. Transcriptomic and IHC analysis confirmed a constant overexpression of CDX2 in ITAC samples, without any specific DNA methylation profile regarding the CDX2 locus. ITAC woodworkers also exhibited a specific transcriptomic profile in their contralateral (non-tumor) olfactory cleft, different from that of other exposed woodworkers, suggesting that they had a different exposure or a different susceptibility. Two top-loci (CACNA1C/CACNA1C-AS1 and SLC26A10) were identified with a hemimethylated profile, but only CACNA1C appeared to be overexpressed both in transcriptomic analysis and in immunohistochemistry.
Several clusters of genes enable the distinction between healthy mucosa and ITAC samples even in contralateral nasal fossa thus paving the way for a simple diagnostic tool for ITAC in male woodworkers. CACNA1C might be considered as a master gene of ITAC and should be further investigated.
NIH ClinicalTrials, NCT0281823, registered May 23 2016, https://www.clinicaltrials.gov/NCT0281823 .
鼻肠型腺癌(ITAC)与慢性木尘暴露密切相关:肠型表型依赖于 CDX2 的过表达,但潜在的分子机制尚不清楚。我们的目标是研究健康非暴露和肿瘤嗅裂黏膜之间的转录组和甲基化差异,并比较非暴露、木尘暴露和 ITAC 黏膜细胞之间的转录组谱。
我们进行了一项前瞻性单中心研究(NCT0281823),纳入了 16 名 ITAC 木工、16 名健康暴露木工和 13 名健康、非暴露、对照者。我们比较了肿瘤样本与健康非暴露样本的转录组和甲基组分析。我们还研究了暴露(无肿瘤)男性木工样本和肿瘤对侧的木尘诱导的转录组修饰。我们同时进行了转录组和甲基组分析,然后,转录组分析集中在甲基组分析中突出的基因上。我们在数据集 GSE17433 上复制了我们的结果。
几个基因簇使健康和 ITAC 样本得以区分。转录组和免疫组化分析证实 CDX2 在 ITAC 样本中持续过表达,而 CDX2 基因座没有特定的 DNA 甲基化模式。ITAC 木工在其对侧(非肿瘤)嗅裂中也表现出特定的转录组谱,与其他暴露木工不同,这表明他们有不同的暴露或不同的易感性。两个顶级基因座(CACNA1C/CACNA1C-AS1 和 SLC26A10)被鉴定为半甲基化模式,但只有 CACNA1C 在转录组分析和免疫组化中均显示过度表达。
即使在对侧鼻腔,几个基因簇也能区分健康黏膜和 ITAC 样本,为男性木工 ITAC 的简单诊断工具铺平了道路。CACNA1C 可能被视为 ITAC 的主基因,应进一步研究。
NIH 临床试验,NCT0281823,2016 年 5 月 23 日注册,https://www.clinicaltrials.gov/NCT0281823。