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. 2022 Oct 25;15:222. doi: 10.1186/s12920-022-01380-z

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© The Author(s) 2022

Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 5 — DNA damage response pathway in the two subgroups and relative drug sensitivity analyses of HCC in the TCGA database. A The expressions of representative genes of DNA damage response pathway in high asparagine metabolism HCC subgroup were significantly higher than the low asparagine metabolism group. B The IC50 of two subgroups in response to sorafenib showed no difference. C The IC50 of high asparagine metabolism subgroup in response to CHEK1 inhibitor AZD7762 and PARP 1/2 inhibitor ABT-888 were lower than the low asparagine metabolism subgroup