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サトウ アツシ
Atsushi Sato
佐藤 淳 所属 応用生物学部 応用生物学科 職種 教授 |
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| 言語種別 | 英語 |
| 発行・発表の年月 | 2025/08 |
| 形態種別 | 学術講演予稿集(学会、研究会を含む) |
| 標題 | Albumin-fused human lactoferrin inhibits lung cancer cell migration by impaired Na+/H+ exchanger 7-driven organelle pH |
| 執筆形態 | 共著 |
| 掲載誌名 | ラクトフェリン2025 |
| 掲載区分 | 国内 |
| 出版社・発行元 | アイ・ケイ コーポレーション |
| 担当区分 | 責任著者 |
| 著者・共著者 | Nopia Hana, Masahiro Kimura, and Atsushi Sato |
| 概要 | The fusion of human serum albumin (HSA) to human lactoferrin (hLF) (here in referred to as hLF-HSA) has strongly exhibited anti-migratory effects through the downregulation of matrix metalloprotease 1 (MMP1) against the human lung adenocarcinoma PC-14 cells. In this study, we report that the upregulation of Na+/H+ exchanger 7 (NHE7) induced by hLF-HSA corresponds to its anti-migratory effects. hLF-HSA showed organelle alkalization via NHE7 upregulation in PC-14 cells, disrupting the organelle pH homeostatic. This disruption of organelle pH homeostasis, particularly in the trans-Golgi network (TGN), leads to the downregulation of MMP1, a key molecule in the anti-migratory activity of hLF-HSA, thereby reducing migration. Moreover, hLF-HSA-induced downregulation of MMP1 subsequently reversed the epithelial-mesenchymal transition (EMT), a process that can promote tumor-initiating potential during cancer metastasis. The reverse process of EMT suppresses PC-14 cell migration. Therefore, hLF-HSA-induced organelle pH dysfunction in cancer cells represents a novel and promising approach to suppressing cancer migration. Further studies on the versatility of hLF-HSA across various cancer cell types are necessary to fully establish its potential as an anti-tumor drug candidate. |
| 外部リンクURL | https://lactoferrin.jp/archive.html |