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Extracellular PKCδ signals to epidermal growth factor receptor for tumor proliferation in liver cancer cells
Protein kinase C delta (PKCδ) is a multifunctional PKC family member and has been implicated in many types of cancers, including liver cancer. Recently, we have reported that PKCδ is secreted from liver cancer cells, and involved in cell proliferation and tumor growth. However, it remains unclear wh...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9277411/ https://www.ncbi.nlm.nih.gov/pubmed/35490382 http://dx.doi.org/10.1111/cas.15386 |
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author | Yamada, Kohji Kizawa, Ryusuke Yoshida, Ayano Koizumi, Rei Motohashi, Saya Shimoyama, Yuya Hannya, Yoshito Yoshida, Saishu Oikawa, Tsunekazu Shimoda, Masayuki Yoshida, Kiyotsugu |
author_facet | Yamada, Kohji Kizawa, Ryusuke Yoshida, Ayano Koizumi, Rei Motohashi, Saya Shimoyama, Yuya Hannya, Yoshito Yoshida, Saishu Oikawa, Tsunekazu Shimoda, Masayuki Yoshida, Kiyotsugu |
author_sort | Yamada, Kohji |
collection | PubMed |
description | Protein kinase C delta (PKCδ) is a multifunctional PKC family member and has been implicated in many types of cancers, including liver cancer. Recently, we have reported that PKCδ is secreted from liver cancer cells, and involved in cell proliferation and tumor growth. However, it remains unclear whether the extracellular PKCδ directly regulates cell surface growth factor receptors. Here, we identify epidermal growth factor receptor (EGFR) as a novel interacting protein of the cell surface PKCδ in liver cancer cells. Imaging studies showed that secreted PKCδ interacted with EGFR‐expressing cells in both autocrine and paracrine manners. Biochemical analysis revealed that PKCδ bound to the extracellular domain of EGFR. We further found that a part of the amino acid sequence on the C‐terminal region of PKCδ was similar to the putative EGFR binding site of EGF. In this regard, the point mutant of PKCδ in the binding site lacked the ability to bind to the extracellular domain of EGFR. Upon an extracellular PKCδ‐EGFR association, ERK1/2 activation, downstream of EGFR signaling, was apparently induced in liver cancer cells. This study indicates that extracellular PKCδ behaves as a growth factor and provides a molecular basis for extracellular PKCδ‐targeting therapy for liver cancer. |
format | Online Article Text |
id | pubmed-9277411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92774112022-07-15 Extracellular PKCδ signals to epidermal growth factor receptor for tumor proliferation in liver cancer cells Yamada, Kohji Kizawa, Ryusuke Yoshida, Ayano Koizumi, Rei Motohashi, Saya Shimoyama, Yuya Hannya, Yoshito Yoshida, Saishu Oikawa, Tsunekazu Shimoda, Masayuki Yoshida, Kiyotsugu Cancer Sci ORIGINAL ARTICLES Protein kinase C delta (PKCδ) is a multifunctional PKC family member and has been implicated in many types of cancers, including liver cancer. Recently, we have reported that PKCδ is secreted from liver cancer cells, and involved in cell proliferation and tumor growth. However, it remains unclear whether the extracellular PKCδ directly regulates cell surface growth factor receptors. Here, we identify epidermal growth factor receptor (EGFR) as a novel interacting protein of the cell surface PKCδ in liver cancer cells. Imaging studies showed that secreted PKCδ interacted with EGFR‐expressing cells in both autocrine and paracrine manners. Biochemical analysis revealed that PKCδ bound to the extracellular domain of EGFR. We further found that a part of the amino acid sequence on the C‐terminal region of PKCδ was similar to the putative EGFR binding site of EGF. In this regard, the point mutant of PKCδ in the binding site lacked the ability to bind to the extracellular domain of EGFR. Upon an extracellular PKCδ‐EGFR association, ERK1/2 activation, downstream of EGFR signaling, was apparently induced in liver cancer cells. This study indicates that extracellular PKCδ behaves as a growth factor and provides a molecular basis for extracellular PKCδ‐targeting therapy for liver cancer. John Wiley and Sons Inc. 2022-05-12 2022-07 /pmc/articles/PMC9277411/ /pubmed/35490382 http://dx.doi.org/10.1111/cas.15386 Text en © 2022 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) 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. |
spellingShingle | ORIGINAL ARTICLES Yamada, Kohji Kizawa, Ryusuke Yoshida, Ayano Koizumi, Rei Motohashi, Saya Shimoyama, Yuya Hannya, Yoshito Yoshida, Saishu Oikawa, Tsunekazu Shimoda, Masayuki Yoshida, Kiyotsugu Extracellular PKCδ signals to epidermal growth factor receptor for tumor proliferation in liver cancer cells |
title | Extracellular PKCδ signals to epidermal growth factor receptor for tumor proliferation in liver cancer cells |
title_full | Extracellular PKCδ signals to epidermal growth factor receptor for tumor proliferation in liver cancer cells |
title_fullStr | Extracellular PKCδ signals to epidermal growth factor receptor for tumor proliferation in liver cancer cells |
title_full_unstemmed | Extracellular PKCδ signals to epidermal growth factor receptor for tumor proliferation in liver cancer cells |
title_short | Extracellular PKCδ signals to epidermal growth factor receptor for tumor proliferation in liver cancer cells |
title_sort | extracellular pkcδ signals to epidermal growth factor receptor for tumor proliferation in liver cancer cells |
topic | ORIGINAL ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9277411/ https://www.ncbi.nlm.nih.gov/pubmed/35490382 http://dx.doi.org/10.1111/cas.15386 |
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