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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2022
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.
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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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