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. 2020 Aug 14;13:112. doi: 10.1186/s12920-020-00762-5

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© The Author(s) 2020

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. 6 — NDC80 and MAD2L1 related signaling analysis. Expression of NDC80 in various human cancers revealed by GEPIA. NDC80 centered PPI network representing the genes most related to NDC80. e Correlation between NDC80 and c MAD2L1, d BUB1B and e AURKA in LUAD revealed by GEPIA (R = 0.67, 0.79, 0.65 respectively). f Expression of MAD2L1 in various human cancers revealed by GEPIA. g MAD2L1 centered PPI network representing the genes most related to MAD2L1. h-j Correlation between MAD2L1 and h NDC80, i BUB1B and j AURKA in LUSC revealed by GEPIA (R = 0.40, 0.46, 0.44 respectively)