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. 2018 Oct 29;41(1):257–269. doi: 10.3892/or.2018.6829

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Copyright: © Yu et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 4. — Differentially expressed exosomal miRs between the fast- and slow-migrated groups. (A) Unsupervised principal component analysis clustered the samples into two groups (separated by the blue line). Ten samples with a fast migration rate and 7 out of 10 samples with a slow migration rate were naturally clustered into two groups. (B) Six exosomal miRs were differentially expressed between fast- and slow-migrated groups. In the fast-migrated group, five of them were downregulated (miR-140-3p, miR-30d-5p, miR-29b-3p, miR-130b-3p and miR-330-5p) and one (miR-296-3p) was upregulated compared with the low-migrated group. miR, microRNA.