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. 2018 Jan 17;11:8. doi: 10.1186/s13048-018-0380-5

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© The Author(s). 2018

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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.

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Fig. 6 — Western blot analysis of MyD88, TRIF, IKK-α, p-IkBα, and NF-kB p65 and fluorescence localization in serous papillary OC. Protein profiles of representative cytosolic (a) and nuclear (c) fractions (50 μg protein) pooled from 5 samples per group. b Individual blots were used for densitometric analysis of the protein levels following normalization to β-actin or Lamin B1. Data are expressed as the mean ± SD. ^* P < 0.05 vs. the OC group. d Merged images of NF-kB p65 immunofluorescence and DAPI nuclear staining in the OC (I), P-MAPA (II), CIS (III), and P-MAPA+CIS (IV) groups (Alexafluor®488, Bar = 10 μm). MyD88: Myeloid differentiation factor 88; TRIF: TLR-associated activator of interferon; IKK-α: inhibitor of NF-kB kinase subunit alpha; p-IkBα: inhibitor of phosphorylated NF-kB subunit alpha; NF-kB p65: NF-kB subunit p65 (RelA)