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. 2022 Sep 15;13:5413. doi: 10.1038/s41467-022-33116-z

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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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 5 — a Tumour volume and survival analysis of sgCtrl and sgUba6 B16-GMCSF tumours in NSG, wild-type (WT) mice (n = 8). b Tumour volume and survival analysis of sgCtrl and sgUba6 B16-GMCSF tumours in WT mice with Ctrl, ICB, or ICB + Ino treatment (n = 8). c Tumour volume and survival analysis of sgCtrl and sgUba6 4T1 tumour-bearing NSG mice (left) or wild-type (WT) mice (right) (n = 10). d Tumour volume and survival analysis of sgCtrl and sgUba6 4T1 tumour-bearing WT mice with Ctrl, ICB, or ICB + Ino treatment (n = 10). Data are presented as mean ± SEM. Statistical significance was determined by ANOVA (tumour volume of a–d) or log-rank (Mantel–Cox) test (survival analysis of a–d). NS no significant. Source data are provided as a Source Data file.