Effects of Ephedra Herb extract on the expression of EGFR-activating mutations and c-Met in non-small-cell lung cancer cell line, H1975, and its combined effects with osimertinib
We previously reported that the combined application of Ephedra Herb extract (EHE) and epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI), erlotinib, is effective in suppressing the growth of erlotinib-resistant non-small-cell lung cancer (NSCLC) cell line, H1993, xenograft tumo...
Gespeichert in:
Veröffentlicht in: | Journal of natural medicines 2023-06, Vol.77 (3), p.523-534 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 534 |
---|---|
container_issue | 3 |
container_start_page | 523 |
container_title | Journal of natural medicines |
container_volume | 77 |
creator | Mori, Eiko Hyuga, Sumiko Hanawa, Toshihiko Naoki, Katsuhiko Odaguchi, Hiroshi |
description | We previously reported that the combined application of Ephedra Herb extract (EHE) and epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI), erlotinib, is effective in suppressing the growth of erlotinib-resistant non-small-cell lung cancer (NSCLC) cell line, H1993, xenograft tumor, and cell proliferation, and that EHE downregulates c-Met and wild-type EGFR in H1993 cells. However, it was unclear whether EHE could affect EGFR with active mutations. Clinically, advanced NSCLC patients who are eligible for EGFR-TKI treatment are those with detected EGFR with activating mutations. Therefore, it is important to clarify the effect of EHE on EGFR with activating mutations. H1975 cells express EGFR with activating mutations, L858R and T790M, and c-Met; this NSCLC cell line was used in the present study. EHE downregulated the expression of EGFR with activating mutations and c-Met, and inhibited autophosphorylation of c-Met. Proliferation of H1975 cells was suppressed by EHE in a concentration-dependent manner. These results suggest that EHE may be effective against NSCLC harboring EGFR with activating mutations. Considering the fact that advanced NSCLC patients, with an EGFR T790M mutation, are currently widely treated with the third-generation EGFR-TKI, osimertinib, we examined the combined effects of osimertinib and EHE on H1975 cells. The osimertinib and EHE combination downregulated the expression of these receptors and suppressed the proliferation of H1975 cells more effectively than did osimertinib alone, suggesting that this combination may be effective in treating patients with advanced NSCLC with the L858R + T790M EGFR mutation and c-Met.
Graphical abstract
Graphical Abstract was created with BioRender.com. |
doi_str_mv | 10.1007/s11418-023-01695-w |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3153180849</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3153180849</sourcerecordid><originalsourceid>FETCH-LOGICAL-c432t-243331e981e47c0e9aafa5331b82790af6208a7b4a2d6993f4cb1f271e3bcfea3</originalsourceid><addsrcrecordid>eNqFkctu1DAUhiNERS_wAiyQJTYsaupbEnuJqmmnUlGlCtaR4xx3XCX2YDsMvBZPiKcZQGIBKx__5zs3_VX1mpL3lJD2IlEqqMSEcUxoo2q8e1adUNnQIin-vMRcEMyF4MfVaUqPhAjGOX1RHfOWCE6pOql-rKwFkxMKFq22GxiiRmuIPYJvOWqTUfAob6B8txFScuW7J6-v7nHJuq86O_-ApjmXIPiEtB-QwR8hI-eRDx6nSY8jNjCOaJwLarQ3ENEiOA_naE1VW58_VbqyiAlTX_QBwWGzncsbFJKbIJZhrn9ZHVk9Jnh1eM-qz1erT5drfHt3fXP54RYbwVnGTPByLChJQbSGgNLa6rpIvWStIto2jEjd9kKzoVGKW2F6allLgffGguZn1bul7zaGLzOk3E0u7ffWHsKcOk5rTiWRQv0XZZIQKqSoZUHf_oU-hjn6ckihGKkJV82eYgtlYkgpgu220U06fu8o6fbmd4v5XTG_ezK_25WiN4fWcz_B8Lvkl9sF4AuQSso_QPwz-x9tfwKEurqo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2820503968</pqid></control><display><type>article</type><title>Effects of Ephedra Herb extract on the expression of EGFR-activating mutations and c-Met in non-small-cell lung cancer cell line, H1975, and its combined effects with osimertinib</title><source>Springer Online Journals - JUSTICE</source><creator>Mori, Eiko ; Hyuga, Sumiko ; Hanawa, Toshihiko ; Naoki, Katsuhiko ; Odaguchi, Hiroshi</creator><creatorcontrib>Mori, Eiko ; Hyuga, Sumiko ; Hanawa, Toshihiko ; Naoki, Katsuhiko ; Odaguchi, Hiroshi</creatorcontrib><description>We previously reported that the combined application of Ephedra Herb extract (EHE) and epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI), erlotinib, is effective in suppressing the growth of erlotinib-resistant non-small-cell lung cancer (NSCLC) cell line, H1993, xenograft tumor, and cell proliferation, and that EHE downregulates c-Met and wild-type EGFR in H1993 cells. However, it was unclear whether EHE could affect EGFR with active mutations. Clinically, advanced NSCLC patients who are eligible for EGFR-TKI treatment are those with detected EGFR with activating mutations. Therefore, it is important to clarify the effect of EHE on EGFR with activating mutations. H1975 cells express EGFR with activating mutations, L858R and T790M, and c-Met; this NSCLC cell line was used in the present study. EHE downregulated the expression of EGFR with activating mutations and c-Met, and inhibited autophosphorylation of c-Met. Proliferation of H1975 cells was suppressed by EHE in a concentration-dependent manner. These results suggest that EHE may be effective against NSCLC harboring EGFR with activating mutations. Considering the fact that advanced NSCLC patients, with an EGFR T790M mutation, are currently widely treated with the third-generation EGFR-TKI, osimertinib, we examined the combined effects of osimertinib and EHE on H1975 cells. The osimertinib and EHE combination downregulated the expression of these receptors and suppressed the proliferation of H1975 cells more effectively than did osimertinib alone, suggesting that this combination may be effective in treating patients with advanced NSCLC with the L858R + T790M EGFR mutation and c-Met.
Graphical abstract
Graphical Abstract was created with BioRender.com.</description><identifier>ISSN: 1340-3443</identifier><identifier>EISSN: 1861-0293</identifier><identifier>DOI: 10.1007/s11418-023-01695-w</identifier><identifier>PMID: 37043119</identifier><language>eng</language><publisher>Singapore: Springer Nature Singapore</publisher><subject>Biomedical and Life Sciences ; Biomedicine ; c-Met protein ; cell lines ; Cell proliferation ; Complementary & Alternative Medicine ; Ephedra ; Epidermal growth factor receptors ; Herbs ; Lung cancer ; lung neoplasms ; Medicinal Chemistry ; Mutation ; neoplasm cells ; Non-small cell lung carcinoma ; Original Paper ; Pharmacology/Toxicology ; Pharmacy ; Plant Sciences ; protein phosphorylation ; Protein-tyrosine kinase ; Small cell lung carcinoma ; Targeted cancer therapy ; xenotransplantation</subject><ispartof>Journal of natural medicines, 2023-06, Vol.77 (3), p.523-534</ispartof><rights>The Author(s) under exclusive licence to The Japanese Society of Pharmacognosy 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. The Author(s) under exclusive licence to The Japanese Society of Pharmacognosy.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c432t-243331e981e47c0e9aafa5331b82790af6208a7b4a2d6993f4cb1f271e3bcfea3</citedby><cites>FETCH-LOGICAL-c432t-243331e981e47c0e9aafa5331b82790af6208a7b4a2d6993f4cb1f271e3bcfea3</cites><orcidid>0000-0002-8863-1557 ; 0000-0002-8323-3680 ; 0000-0001-7612-2870 ; 0000-0002-9637-1388</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11418-023-01695-w$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11418-023-01695-w$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37043119$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mori, Eiko</creatorcontrib><creatorcontrib>Hyuga, Sumiko</creatorcontrib><creatorcontrib>Hanawa, Toshihiko</creatorcontrib><creatorcontrib>Naoki, Katsuhiko</creatorcontrib><creatorcontrib>Odaguchi, Hiroshi</creatorcontrib><title>Effects of Ephedra Herb extract on the expression of EGFR-activating mutations and c-Met in non-small-cell lung cancer cell line, H1975, and its combined effects with osimertinib</title><title>Journal of natural medicines</title><addtitle>J Nat Med</addtitle><addtitle>J Nat Med</addtitle><description>We previously reported that the combined application of Ephedra Herb extract (EHE) and epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI), erlotinib, is effective in suppressing the growth of erlotinib-resistant non-small-cell lung cancer (NSCLC) cell line, H1993, xenograft tumor, and cell proliferation, and that EHE downregulates c-Met and wild-type EGFR in H1993 cells. However, it was unclear whether EHE could affect EGFR with active mutations. Clinically, advanced NSCLC patients who are eligible for EGFR-TKI treatment are those with detected EGFR with activating mutations. Therefore, it is important to clarify the effect of EHE on EGFR with activating mutations. H1975 cells express EGFR with activating mutations, L858R and T790M, and c-Met; this NSCLC cell line was used in the present study. EHE downregulated the expression of EGFR with activating mutations and c-Met, and inhibited autophosphorylation of c-Met. Proliferation of H1975 cells was suppressed by EHE in a concentration-dependent manner. These results suggest that EHE may be effective against NSCLC harboring EGFR with activating mutations. Considering the fact that advanced NSCLC patients, with an EGFR T790M mutation, are currently widely treated with the third-generation EGFR-TKI, osimertinib, we examined the combined effects of osimertinib and EHE on H1975 cells. The osimertinib and EHE combination downregulated the expression of these receptors and suppressed the proliferation of H1975 cells more effectively than did osimertinib alone, suggesting that this combination may be effective in treating patients with advanced NSCLC with the L858R + T790M EGFR mutation and c-Met.
Graphical abstract
Graphical Abstract was created with BioRender.com.</description><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>c-Met protein</subject><subject>cell lines</subject><subject>Cell proliferation</subject><subject>Complementary & Alternative Medicine</subject><subject>Ephedra</subject><subject>Epidermal growth factor receptors</subject><subject>Herbs</subject><subject>Lung cancer</subject><subject>lung neoplasms</subject><subject>Medicinal Chemistry</subject><subject>Mutation</subject><subject>neoplasm cells</subject><subject>Non-small cell lung carcinoma</subject><subject>Original Paper</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><subject>Plant Sciences</subject><subject>protein phosphorylation</subject><subject>Protein-tyrosine kinase</subject><subject>Small cell lung carcinoma</subject><subject>Targeted cancer therapy</subject><subject>xenotransplantation</subject><issn>1340-3443</issn><issn>1861-0293</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFkctu1DAUhiNERS_wAiyQJTYsaupbEnuJqmmnUlGlCtaR4xx3XCX2YDsMvBZPiKcZQGIBKx__5zs3_VX1mpL3lJD2IlEqqMSEcUxoo2q8e1adUNnQIin-vMRcEMyF4MfVaUqPhAjGOX1RHfOWCE6pOql-rKwFkxMKFq22GxiiRmuIPYJvOWqTUfAob6B8txFScuW7J6-v7nHJuq86O_-ApjmXIPiEtB-QwR8hI-eRDx6nSY8jNjCOaJwLarQ3ENEiOA_naE1VW58_VbqyiAlTX_QBwWGzncsbFJKbIJZhrn9ZHVk9Jnh1eM-qz1erT5drfHt3fXP54RYbwVnGTPByLChJQbSGgNLa6rpIvWStIto2jEjd9kKzoVGKW2F6allLgffGguZn1bul7zaGLzOk3E0u7ffWHsKcOk5rTiWRQv0XZZIQKqSoZUHf_oU-hjn6ckihGKkJV82eYgtlYkgpgu220U06fu8o6fbmd4v5XTG_ezK_25WiN4fWcz_B8Lvkl9sF4AuQSso_QPwz-x9tfwKEurqo</recordid><startdate>20230601</startdate><enddate>20230601</enddate><creator>Mori, Eiko</creator><creator>Hyuga, Sumiko</creator><creator>Hanawa, Toshihiko</creator><creator>Naoki, Katsuhiko</creator><creator>Odaguchi, Hiroshi</creator><general>Springer Nature Singapore</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0002-8863-1557</orcidid><orcidid>https://orcid.org/0000-0002-8323-3680</orcidid><orcidid>https://orcid.org/0000-0001-7612-2870</orcidid><orcidid>https://orcid.org/0000-0002-9637-1388</orcidid></search><sort><creationdate>20230601</creationdate><title>Effects of Ephedra Herb extract on the expression of EGFR-activating mutations and c-Met in non-small-cell lung cancer cell line, H1975, and its combined effects with osimertinib</title><author>Mori, Eiko ; Hyuga, Sumiko ; Hanawa, Toshihiko ; Naoki, Katsuhiko ; Odaguchi, Hiroshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c432t-243331e981e47c0e9aafa5331b82790af6208a7b4a2d6993f4cb1f271e3bcfea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>c-Met protein</topic><topic>cell lines</topic><topic>Cell proliferation</topic><topic>Complementary & Alternative Medicine</topic><topic>Ephedra</topic><topic>Epidermal growth factor receptors</topic><topic>Herbs</topic><topic>Lung cancer</topic><topic>lung neoplasms</topic><topic>Medicinal Chemistry</topic><topic>Mutation</topic><topic>neoplasm cells</topic><topic>Non-small cell lung carcinoma</topic><topic>Original Paper</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic><topic>Plant Sciences</topic><topic>protein phosphorylation</topic><topic>Protein-tyrosine kinase</topic><topic>Small cell lung carcinoma</topic><topic>Targeted cancer therapy</topic><topic>xenotransplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mori, Eiko</creatorcontrib><creatorcontrib>Hyuga, Sumiko</creatorcontrib><creatorcontrib>Hanawa, Toshihiko</creatorcontrib><creatorcontrib>Naoki, Katsuhiko</creatorcontrib><creatorcontrib>Odaguchi, Hiroshi</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Journal of natural medicines</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mori, Eiko</au><au>Hyuga, Sumiko</au><au>Hanawa, Toshihiko</au><au>Naoki, Katsuhiko</au><au>Odaguchi, Hiroshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Ephedra Herb extract on the expression of EGFR-activating mutations and c-Met in non-small-cell lung cancer cell line, H1975, and its combined effects with osimertinib</atitle><jtitle>Journal of natural medicines</jtitle><stitle>J Nat Med</stitle><addtitle>J Nat Med</addtitle><date>2023-06-01</date><risdate>2023</risdate><volume>77</volume><issue>3</issue><spage>523</spage><epage>534</epage><pages>523-534</pages><issn>1340-3443</issn><eissn>1861-0293</eissn><abstract>We previously reported that the combined application of Ephedra Herb extract (EHE) and epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI), erlotinib, is effective in suppressing the growth of erlotinib-resistant non-small-cell lung cancer (NSCLC) cell line, H1993, xenograft tumor, and cell proliferation, and that EHE downregulates c-Met and wild-type EGFR in H1993 cells. However, it was unclear whether EHE could affect EGFR with active mutations. Clinically, advanced NSCLC patients who are eligible for EGFR-TKI treatment are those with detected EGFR with activating mutations. Therefore, it is important to clarify the effect of EHE on EGFR with activating mutations. H1975 cells express EGFR with activating mutations, L858R and T790M, and c-Met; this NSCLC cell line was used in the present study. EHE downregulated the expression of EGFR with activating mutations and c-Met, and inhibited autophosphorylation of c-Met. Proliferation of H1975 cells was suppressed by EHE in a concentration-dependent manner. These results suggest that EHE may be effective against NSCLC harboring EGFR with activating mutations. Considering the fact that advanced NSCLC patients, with an EGFR T790M mutation, are currently widely treated with the third-generation EGFR-TKI, osimertinib, we examined the combined effects of osimertinib and EHE on H1975 cells. The osimertinib and EHE combination downregulated the expression of these receptors and suppressed the proliferation of H1975 cells more effectively than did osimertinib alone, suggesting that this combination may be effective in treating patients with advanced NSCLC with the L858R + T790M EGFR mutation and c-Met.
Graphical abstract
Graphical Abstract was created with BioRender.com.</abstract><cop>Singapore</cop><pub>Springer Nature Singapore</pub><pmid>37043119</pmid><doi>10.1007/s11418-023-01695-w</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-8863-1557</orcidid><orcidid>https://orcid.org/0000-0002-8323-3680</orcidid><orcidid>https://orcid.org/0000-0001-7612-2870</orcidid><orcidid>https://orcid.org/0000-0002-9637-1388</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1340-3443 |
ispartof | Journal of natural medicines, 2023-06, Vol.77 (3), p.523-534 |
issn | 1340-3443 1861-0293 |
language | eng |
recordid | cdi_proquest_miscellaneous_3153180849 |
source | Springer Online Journals - JUSTICE |
subjects | Biomedical and Life Sciences Biomedicine c-Met protein cell lines Cell proliferation Complementary & Alternative Medicine Ephedra Epidermal growth factor receptors Herbs Lung cancer lung neoplasms Medicinal Chemistry Mutation neoplasm cells Non-small cell lung carcinoma Original Paper Pharmacology/Toxicology Pharmacy Plant Sciences protein phosphorylation Protein-tyrosine kinase Small cell lung carcinoma Targeted cancer therapy xenotransplantation |
title | Effects of Ephedra Herb extract on the expression of EGFR-activating mutations and c-Met in non-small-cell lung cancer cell line, H1975, and its combined effects with osimertinib |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T06%3A54%3A02IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effects%20of%20Ephedra%20Herb%20extract%20on%20the%20expression%20of%20EGFR-activating%20mutations%20and%20c-Met%20in%20non-small-cell%20lung%20cancer%20cell%20line,%20H1975,%20and%20its%20combined%20effects%20with%20osimertinib&rft.jtitle=Journal%20of%20natural%20medicines&rft.au=Mori,%20Eiko&rft.date=2023-06-01&rft.volume=77&rft.issue=3&rft.spage=523&rft.epage=534&rft.pages=523-534&rft.issn=1340-3443&rft.eissn=1861-0293&rft_id=info:doi/10.1007/s11418-023-01695-w&rft_dat=%3Cproquest_cross%3E3153180849%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2820503968&rft_id=info:pmid/37043119&rfr_iscdi=true |