Blohmer Martin, Cheek David M, Hung Wei-Ting, Kessler Maria, Chatzidimitriou Foivos, Wang Jiahe, Hung William, Lee I-Hsiu, Gorelick Alexander N, Wassenaar Emma Ce, Yang Ching-Yeuh, Yeh Yi-Chen, Ho Hsiang-Ling, Speiser Dorothee, Karsten Maria M, Lanuti Michael, Pai Sara I, Kranenburg Onno, Lennerz Jochen K, Chou Teh-Ying, Kloor Matthias, Naxerova Kamila
Department of Genetics, Harvard Medical School, Boston, MA, USA.
Center for Systems Biology, Massachusetts General Hospital Research Institute and Harvard Medical School, Boston, MA, USA.
Nat Genet. 2025 Mar;57(3):706-717. doi: 10.1038/s41588-025-02078-5. Epub 2025 Feb 4.
Cell division drives somatic evolution but is challenging to quantify. We developed a framework to count cell divisions with DNA replication-related mutations in polyguanine homopolymers. Analyzing 505 samples from 37 patients, we studied the milestones of colorectal cancer evolution. Primary tumors diversify at ~250 divisions from the founder cell, while distant metastasis divergence occurs significantly later, at ~500 divisions. Notably, distant but not lymph node metastases originate from primary tumor regions that have undergone surplus divisions, tying subclonal expansion to metastatic capacity. Then, we analyzed a cohort of 73 multifocal lung cancers and showed that the cell division burden of the tumors' common ancestor distinguishes independent primary tumors from intrapulmonary metastases and correlates with patient survival. In lung cancer too, metastatic capacity is tied to more extensive proliferation. The cell division history of human cancers is easily accessible using our simple framework and contains valuable biological and clinical information.
细胞分裂推动体细胞进化,但难以进行量化。我们开发了一个框架,用于通过多聚鸟嘌呤同聚物中与DNA复制相关的突变来计数细胞分裂。通过分析来自37名患者的505个样本,我们研究了结直肠癌进化的各个阶段。原发性肿瘤从起始细胞开始经过约250次分裂后开始分化,而远处转移的分化则明显较晚,约在500次分裂时发生。值得注意的是,远处转移而非淋巴结转移起源于经历了过多分裂的原发性肿瘤区域,将亚克隆扩增与转移能力联系起来。然后,我们分析了一组73例多灶性肺癌,结果表明肿瘤共同祖先的细胞分裂负担可区分独立原发性肿瘤和肺内转移瘤,并与患者生存率相关。在肺癌中,转移能力也与更广泛的增殖有关。利用我们这个简单的框架可以轻松获取人类癌症的细胞分裂历史,其中包含有价值的生物学和临床信息。