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dc.contributor.authorLi, Weien
dc.contributor.authorKawaguchi, Kosukeen
dc.contributor.authorTanaka, Sunaoen
dc.contributor.authorHe, Chenfengen
dc.contributor.authorMaeshima, Yurinaen
dc.contributor.authorSuzuki, Eijien
dc.contributor.authorToi, Masakazuen
dc.contributor.alternative李, 威ja
dc.contributor.alternative河口, 浩介ja
dc.contributor.alternative田中, 直ja
dc.contributor.alternative何, 晨風ja
dc.contributor.alternative前島, 佑里奈ja
dc.contributor.alternative鈴木, 栄治ja
dc.contributor.alternative戸井, 雅和ja
dc.date.accessioned2023-11-27T06:02:04Z-
dc.date.available2023-11-27T06:02:04Z-
dc.date.issued2023-11-22-
dc.identifier.urihttp://hdl.handle.net/2433/286180-
dc.descriptionがん治療薬による乳がん細胞の老化とpH調整の解明 --新規細胞老化のメカニズム解明に貢献--. 京都大学プレスリリース. 2023-11-27.ja
dc.description.abstractSeveral chemotherapeutic drugs induce senescence in cancer cells; however, the mechanisms underlying intracellular pH dysregulation in senescent cells remain unclear. Adenosine triphosphatase H+ transporting accessory protein 2 (ATP6AP2) plays a critical role in maintaining pH homeostasis in cellular compartments. Herein, we report the regulatory role of ATP6AP2 in senescent breast cancer cells treated with doxorubicin (Doxo) and abemaciclib (Abe). A decline in ATP6AP2 triggers aberrant pH levels that impair lysosomal function and cause immune profile changes in senescent breast cancer cells. Doxo and Abe elicited a stable senescent phenotype and altered the expression of senescence-related genes. Additionally, senescent cells show altered inflammatory and immune transcriptional profiles due to reprogramming of the senescence-associated secretory phenotype. These findings elucidate ATP6AP2-mediated cellular pH regulation and suggest a potential link in immune profile alteration during therapy-induced senescence in breast cancer cells, providing insights into the mechanisms involved in the senescence response to anticancer therapy.en
dc.language.isoeng-
dc.publisherSpringer Natureen
dc.rights© The Author(s) 2023en
dc.rightsThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/-
dc.subjectBreast canceren
dc.subjectSenescenceen
dc.titleCellular senescence triggers intracellular acidification and lysosomal pH alkalinized via ATP6AP2 attenuation in breast cancer cellsen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleCommunications Biologyen
dc.identifier.volume6-
dc.relation.doi10.1038/s42003-023-05433-6-
dc.textversionpublisher-
dc.identifier.artnum1147-
dc.addressDepartment of Breast Surgery, Kyoto University Graduate School of Medicineen
dc.addressDepartment of Breast Surgery, Kyoto University Graduate School of Medicineen
dc.addressDepartment of Breast Surgery, Kyoto University Graduate School of Medicineen
dc.addressDepartment of Breast Surgery, Kyoto University Graduate School of Medicineen
dc.addressDepartment of Breast Surgery, Kyoto University Graduate School of Medicineen
dc.addressKobe City Medical Center General Hospitalen
dc.addressDepartment of Breast Surgery, Kyoto University Graduate School of Medicineen
dc.identifier.pmid37993606-
dc.relation.urlhttps://www.kyoto-u.ac.jp/ja/research-news/2023-11-27-
dcterms.accessRightsopen access-
dc.identifier.eissn2399-3642-
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