Rutgers Cancer Institute of New Jersey, Rutgers the State University of New Jersey, New Brunswick, NJ 08901, USA.
University of Miami, Coral Gables, FL 33124, USA.
Cell Rep. 2019 Nov 19;29(8):2164-2174.e5. doi: 10.1016/j.celrep.2019.10.045.
Impacts of genetic and non-genetic intra-tumor heterogeneity (ITH) on tumor phenotypes and evolvability remain debated. We analyze ITH in lung squamous cell carcinoma at the levels of genome, transcriptome, and tumor-immune interactions and histopathological characteristics by multi-region bulk and single-cell sequencing. Genomic heterogeneity alone is a weak indicator of intra-tumor non-genetic heterogeneity at immune and transcriptomic levels that impact multiple cancer-related pathways, including those related to proliferation and inflammation, which in turn contribute to intra-tumor regional differences in histopathology and subtype classification. Tumor subclones have substantial differences in proliferation score, suggestive of non-neutral clonal dynamics. Proliferation and other cancer-related pathways also show intra-tumor regional differences, sometimes even within the same subclones. Neo-epitope burden negatively correlates with immune infiltration, indicating immune-mediated purifying selection on somatic mutations. Taken together, our observations suggest that non-genetic heterogeneity is a major determinant of heterogeneity in histopathological characteristics and impacts evolutionary dynamics in lung cancer.
遗传和非遗传肿瘤内异质性(ITH)对肿瘤表型和可进化性的影响仍存在争议。我们通过多区域批量和单细胞测序分析了肺鳞癌在基因组、转录组和肿瘤免疫相互作用以及组织病理学特征方面的 ITH。仅基因组异质性是免疫和转录组水平上肿瘤内非遗传异质性的一个弱指标,这些异质性影响多个与癌症相关的途径,包括与增殖和炎症相关的途径,这反过来又导致组织病理学和亚型分类的肿瘤内区域差异。肿瘤亚克隆在增殖评分上存在显著差异,提示非中性克隆动力学。增殖和其他与癌症相关的途径也显示出肿瘤内区域差异,有时甚至在同一亚克隆内。新表位负担与免疫浸润呈负相关,表明体细胞突变受到免疫介导的净化选择。总之,我们的观察结果表明,非遗传异质性是组织病理学特征异质性的主要决定因素,并影响肺癌的进化动态。