Tuffaha Marwa Z, Castellano David, Colome Claudia Serrano, Gutenkunst Ryan N, Wahl Lindi M
Department of Mathematics, Western University, London, Ontario N6A 5B7, Canada.
Department of Molecular and Cellular Biology, University of Arizona, Tucson, Arizona 85721, USA.
bioRxiv. 2024 Nov 26:2024.04.30.591900. doi: 10.1101/2024.04.30.591900.
Cancer is an evolutionary disease driven by mutations in asexually-reproducing somatic cells. In asexual microbes, bias reversals in the mutation spectrum can speed adaptation by increasing access to previously undersampled beneficial mutations. By analyzing tumors from 20 tissues, along with normal tissue and the germline, we demonstrate this effect in cancer. Non-hypermutated tumors reverse the germline mutation bias and have consistent spectra across tissues. These spectra changes carry the signature of hypoxia, and they facilitate positive selection in cancer genes. Hypermutated and non-hypermutated tumors thus acquire driver mutations differently: hypermutated tumors by higher mutation rates and non-hypermutated tumors by changing the mutation spectrum to reverse the germline mutation bias.
癌症是一种由无性繁殖的体细胞中的突变驱动的进化性疾病。在无性繁殖的微生物中,突变谱中的偏差反转可以通过增加获得先前采样不足的有益突变的机会来加速适应。通过分析来自20种组织的肿瘤以及正常组织和种系,我们在癌症中证明了这种效应。非高突变肿瘤会逆转种系突变偏差,并且在不同组织中具有一致的突变谱。这些谱变化带有缺氧的特征,并且它们促进癌症基因中的正选择。因此,高突变和非高突变肿瘤获得驱动突变的方式不同:高突变肿瘤通过更高的突变率,而非高突变肿瘤则通过改变突变谱来逆转种系突变偏差。