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. 2022 Apr 19;41:148. doi: 10.1186/s13046-022-02354-w

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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. 1 — SEMA6A is a prognostic indicator in BRAF-mut melanoma patients. A: SEMA6A Immunohistochemical assessment in BRAF-wt and BRAF-mut melanoma specimens of RECI1 cohort. Pearson’s Chi-square test revealed a significant association between SEMA6A expression and BRAF mutation (p < 0,0001). B: Representative sections from 2 BRAF-wt and 2 BRAF-mut melanoma patients, stained with anti-SEMA6A antibody. C: Progression-free Survival (PFS) and D: Overall Survival (OS) in patients with with high and low SEMA6A (BRAF-mut advanced melanoma). E: Relapse-free survival (RFS) in patients with high and low SEMA6A (BRAF-mut early melanoma) from the cohorts TCGA and DFCI