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. 2022 Nov 16;12:19660. doi: 10.1038/s41598-022-24137-1

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© The Author(s) 2022

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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Vĸ*MYC MM progression is impaired in mice lacking functional ARG1 in myeloid cells. Arg1^flox (n = 17) and myelo Arg1 KO mice (n = 13) were inoculated i.v. with 1 × 10⁶ of Vĸ*MYC cells. (A) Fraction 6 (monoclonal protein)-to-fraction 1 (albumins) ratio in time (1, 3 and 5 weeks after MM cells inoculation); means ± SD. P-values were calculated with one-way ANOVA with Dunnett’s post-hoc test. (B) Animal survival curve. P-value was calculated with log-rank test.