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A peptide derived from adaptor protein STAP-2 inhibits tumor progression by downregulating epidermal growth factor receptor signaling
Signal-transducing adaptor family member-2 (STAP-2) is an adaptor protein that regulates various intracellular signals. We previously demonstrated that STAP-2 binds to epidermal growth factor receptor (EGFR) and facilitates its stability and activation of EGFR signaling in prostate cancer cells. Inh...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9800302/ https://www.ncbi.nlm.nih.gov/pubmed/36410436 http://dx.doi.org/10.1016/j.jbc.2022.102724 |
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author | Maemoto, Taiga Kitai, Yuichi Takahashi, Runa Shoji, Haruka Yamada, Shunsuke Takei, Shiho Ito, Daiki Muromoto, Ryuta Kashiwakura, Jun-ichi Handa, Haruka Hashimoto, Ari Hashimoto, Shigeru Ose, Toyoyuki Oritani, Kenji Matsuda, Tadashi |
author_facet | Maemoto, Taiga Kitai, Yuichi Takahashi, Runa Shoji, Haruka Yamada, Shunsuke Takei, Shiho Ito, Daiki Muromoto, Ryuta Kashiwakura, Jun-ichi Handa, Haruka Hashimoto, Ari Hashimoto, Shigeru Ose, Toyoyuki Oritani, Kenji Matsuda, Tadashi |
author_sort | Maemoto, Taiga |
collection | PubMed |
description | Signal-transducing adaptor family member-2 (STAP-2) is an adaptor protein that regulates various intracellular signals. We previously demonstrated that STAP-2 binds to epidermal growth factor receptor (EGFR) and facilitates its stability and activation of EGFR signaling in prostate cancer cells. Inhibition of this interaction may be a promising direction for cancer treatment. Here, we found that 2D5 peptide, a STAP-2–derived peptide, blocked STAP-2–EGFR interactions and suppressed EGFR-mediated proliferation in several cancer cell lines. 2D5 peptide inhibited tumor growth of human prostate cancer cell line DU145 and human lung cancer cell line A549 in murine xenograft models. Additionally, we determined that EGFR signaling and its stability were decreased by 2D5 peptide treatment during EGF stimulation. In conclusion, our study shows that 2D5 peptide is a novel anticancer peptide that inhibits STAP-2–mediated activation of EGFR signaling and suppresses prostate and lung cancer progression. |
format | Online Article Text |
id | pubmed-9800302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-98003022023-01-03 A peptide derived from adaptor protein STAP-2 inhibits tumor progression by downregulating epidermal growth factor receptor signaling Maemoto, Taiga Kitai, Yuichi Takahashi, Runa Shoji, Haruka Yamada, Shunsuke Takei, Shiho Ito, Daiki Muromoto, Ryuta Kashiwakura, Jun-ichi Handa, Haruka Hashimoto, Ari Hashimoto, Shigeru Ose, Toyoyuki Oritani, Kenji Matsuda, Tadashi J Biol Chem Research Article Signal-transducing adaptor family member-2 (STAP-2) is an adaptor protein that regulates various intracellular signals. We previously demonstrated that STAP-2 binds to epidermal growth factor receptor (EGFR) and facilitates its stability and activation of EGFR signaling in prostate cancer cells. Inhibition of this interaction may be a promising direction for cancer treatment. Here, we found that 2D5 peptide, a STAP-2–derived peptide, blocked STAP-2–EGFR interactions and suppressed EGFR-mediated proliferation in several cancer cell lines. 2D5 peptide inhibited tumor growth of human prostate cancer cell line DU145 and human lung cancer cell line A549 in murine xenograft models. Additionally, we determined that EGFR signaling and its stability were decreased by 2D5 peptide treatment during EGF stimulation. In conclusion, our study shows that 2D5 peptide is a novel anticancer peptide that inhibits STAP-2–mediated activation of EGFR signaling and suppresses prostate and lung cancer progression. American Society for Biochemistry and Molecular Biology 2022-11-19 /pmc/articles/PMC9800302/ /pubmed/36410436 http://dx.doi.org/10.1016/j.jbc.2022.102724 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Article Maemoto, Taiga Kitai, Yuichi Takahashi, Runa Shoji, Haruka Yamada, Shunsuke Takei, Shiho Ito, Daiki Muromoto, Ryuta Kashiwakura, Jun-ichi Handa, Haruka Hashimoto, Ari Hashimoto, Shigeru Ose, Toyoyuki Oritani, Kenji Matsuda, Tadashi A peptide derived from adaptor protein STAP-2 inhibits tumor progression by downregulating epidermal growth factor receptor signaling |
title | A peptide derived from adaptor protein STAP-2 inhibits tumor progression by downregulating epidermal growth factor receptor signaling |
title_full | A peptide derived from adaptor protein STAP-2 inhibits tumor progression by downregulating epidermal growth factor receptor signaling |
title_fullStr | A peptide derived from adaptor protein STAP-2 inhibits tumor progression by downregulating epidermal growth factor receptor signaling |
title_full_unstemmed | A peptide derived from adaptor protein STAP-2 inhibits tumor progression by downregulating epidermal growth factor receptor signaling |
title_short | A peptide derived from adaptor protein STAP-2 inhibits tumor progression by downregulating epidermal growth factor receptor signaling |
title_sort | peptide derived from adaptor protein stap-2 inhibits tumor progression by downregulating epidermal growth factor receptor signaling |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9800302/ https://www.ncbi.nlm.nih.gov/pubmed/36410436 http://dx.doi.org/10.1016/j.jbc.2022.102724 |
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