Somatic Mitochondrial DNA Mutations in Diffuse Large B-Cell Lymphoma

• Published in: Scientific reports Vol. 8; no. 1; pp. 3623 - 9
• Main Authors: Zeng, Andy G. X., Leung, Andy C. Y., Brooks-Wilson, Angela R.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 26.02.2018; Nature Publishing Group
• Subjects: 45; 631/208/69; 631/208/726/2129; 631/208/726/649/2219; 692/4028/67/1990/291/1621/1915; Amino acid sequence; B-cell lymphoma; Cancer; Genomes; Heteroplasmy; Humanities and Social Sciences; Lymphocytes B; Lymphoma; Mitochondrial DNA; multidisciplinary; Mutagenesis; Mutation; Replication; Science; Science (multidisciplinary); Tumors
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-018-21844-6

Diffuse Large B-Cell Lymphoma (DLBCL) is an aggressive hematological cancer for which mitochondrial metabolism may play an important role. Mitochondrial DNA (mtDNA) encodes crucial mitochondrial proteins, yet the relationship between mtDNA and DLBCL remains unclear. We analyzed the functional consequences and mutational spectra of mtDNA somatic mutations and private constitutional variants in 40 DLBCL tumour-normal pairs. While private constitutional variants occurred frequently in the D-Loop, somatic mutations were randomly distributed across the mitochondrial genome. Heteroplasmic constitutional variants showed a trend towards loss of heteroplasmy in the corresponding tumour regardless of whether the reference or variant allele was being lost, suggesting that these variants are selectively neutral. The mtDNA mutational spectrum showed minimal support for ROS damage and revealed strand asymmetry with increased C > T and A > G transitions on the heavy strand, consistent with a replication-associated mode of mutagenesis. These heavy strand transitions carried higher proportions of amino acid changes – which were also more pathogenic – than equivalent substitutions on the light strand. Taken together, endogenous replication-associated events underlie mtDNA mutagenesis in DLBCL and preferentially generate functionally consequential mutations. Yet mtDNA somatic mutations remain selectively neutral, suggesting that mtDNA-encoded mitochondrial functions may not play an important role in DLBCL.