L-type amino acid transporter 1 inhibitor JPH203 as a new therapeutic target for castration resistant prostate cancer treatment
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- Shinpei Saito
- Dept Pharmacol, Chiba Univ Grad Sch of Med Dept. Urology, Chiba Univ.
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- Sakamoto Shinichi
- Dept. Urology, Chiba Univ.
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- Hamaguchi Norie
- Dept Pharmacol, Chiba Univ Grad Sch of Med
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- Saito Shota
- Dept Pharmacol, Chiba Univ Grad Sch of Med
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- Pae Sangjon
- Dept Pharmacol, Chiba Univ Grad Sch of Med Dept. Urology, Chiba Univ.
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- Reien Yoshie
- Dept Pharmacol, Chiba Univ Grad Sch of Med
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- Hirayama Yuri
- Dept Pharmacol, Chiba Univ Grad Sch of Med
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- Hashimoto Hirofumi
- Dept Pharmacol, Chiba Univ Grad Sch of Med
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- Ichikawa Tomohiko
- Dept. Urology, Chiba Univ.
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- Anzai Naohiko
- Dept Pharmacol, Chiba Univ Grad Sch of Med
Bibliographic Information
- Other Title
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- 去勢抵抗性前立腺癌におけるアミノ酸トランスポーターLAT1選択的阻害薬JPH203の効果
Abstract
<p>L-type amino acid transporter 1 (LAT1) plays a role in transporting essential amino acids including leucine, which regulates the mTOR signaling pathway. Here, we studied the expression profile and functional role of LAT1 in prostate cancer using JPH203, a specific inhibitor of LAT1. LAT1 was highly expressed in castration-resistant prostate cancer (CRPC) cell lines including C4-2 and PC-3, while poorly expressed in castration sensitive LNCaP cells. 5 μ M of JPH203 significantly blocked 14C leucine uptake in CRPC cells, while not affected in LNCaP cells. JPH203 inhibited cell migration at 30 μ M in CRPC cells, while not affected in LNCaP cells. Combination of JPH203 30 μ M and Enzalutamide 10 μ M additively blocked the cell proliferation in CRPC cells. RNA sequence identified CD24 as a novel downstream target of JPH203 in C4-2 cells. SiCD24 blocked cell migration in C4-2 cells via blocking phosphorylation of GSK3β and activating phosphorylation of β catenin. JPH203 25mg/kg significantly inhibited tumor growth in the C4-2 xenograft nude mouse model. Targeting LAT1 by JPH203 may represent a novel therapeutic option in CRPC.</p><p></p>
Journal
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- Proceedings for Annual Meeting of The Japanese Pharmacological Society
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Proceedings for Annual Meeting of The Japanese Pharmacological Society 96 (0), 3-B-P-262-, 2022
Japanese Pharmacological Society
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Keywords
Details 詳細情報について
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- CRID
- 1390857512439268224
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- ISSN
- 24354953
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- Text Lang
- ja
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- Data Source
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- JaLC
- Crossref
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- Abstract License Flag
- Disallowed