Temozolomide (TMZ), a DNA alkylator, is a chemotherapeutic agent for brain tumors, but the treatment induces a distinct pattern of mutations, known as a cancer mutational signature SBS11. Although the correlation between TMZ treatment and SBS11 mutations is very clear, the precise biochemical mechanisms that cause SBS11 have not been elucidated. TMZ can alkylate DNA at several locations, among which O⁶-methylguanine (O⁶me-G) is believed to be most toxic. In this study, we reconstituted potential biochemical processes of TMZ-induced mutagenesis in vitro, including TMZ-induced DNA damage and subsequent DNA synthesis by various DNA polymerases. Next generation sequencing of the DNA products revealed mutations with a similar spectrum to SBS11. Efficient production of the SBS11-like mutation spectra required DNA in double-stranded form and multiple exposures to TMZ. Replicative polymerase δ alone generated SBS11-like mutations on the damaged DNA. Most SBS11-like mutations were sensitive to methyl guanine methyltransferase (MGMT) treatment, indicating that the mutations are formed on O⁶me-G modifications. Human Pol η reduced the SBS11-like mutations, indicating its suppressive role in TMZ-induced mutagenesis. Yeast Pol ζ and human Pol κ generated distinct mutations unrelated to SBS11.

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Journal Article

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Sanyal MR, Sugiyama T

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