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. 2022 Jan 19;12:974. doi: 10.1038/s41598-021-04618-5

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Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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(A) γ-H2AX antibody staining was performed in formalin-fixed tumor tissue for each group at the completion of treatment. DNA damage was significantly increased in the M3814 + IR group in comparison to vehicle alone (p < 0.01). (B) Micrographs of γ-H2AX antibody staining in each group.