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Yoshida, Saori Preliminary Examination Room, Okayama University Hospital
Kawai, Hotaka Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Soe, Yamin Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Eain, Htoo Shwe Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Sanou, Sho Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Takabatake, Kiyofumi Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University Kaken ID publons researchmap
Takeshita, Yohei Department of Oral and Maxillofacial Radiology, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Hisatomi, Miki Department of Oral and Maxillofacial Radiology, Okayama University Hospital Kaken ID publons researchmap
Nagatsuka, Hitoshi Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University Kaken ID publons researchmap
Asaumi, Junichi Department of Oral and Maxillofacial Radiology, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Yanagi, Yoshinobu Preliminary Examination Room, Okayama University Hospital
Abstract
Cisplatin is a platinum-based compound that is widely used for treating inoperable oral squamous cell carcinoma (OSCC) in Japan; however, resistance to cisplatin presents a challenge and innovative approaches are required. We aimed to investigate the therapeutic potential of targeting the chemokine receptor CXCR4, which is involved in angiogenesis and tumor progression, using the CXCR4 inhibitor AMD3100, in combination with cisplatin. AMD3100 induced necrosis and bleeding in OSCC xenografts by inhibiting angiogenesis. We investigated the combined ability of AMD3100 plus cisplatin to enhance the antitumor effect in cisplatin-resistant OSCC. An MTS assay identified HSC-2 cells as cisplatin-resistant cells in vitro. Mice treated with the cisplatin-AMD combination exhibited the most significant reduction in tumor volume, accompanied by extensive hemorrhage and necrosis. Histological examination indicated thin and short tumor vessels in the AMD and cisplatin–AMD groups. These results indicated that cisplatin and AMD3100 had synergistic antitumor effects, highlighting their potential for vascular therapy of refractory OSCC. Antitumor vascular therapy using cisplatin combined with a CXCR4 inhibitor provides a novel strategy for addressing cisplatin-resistant OSCC.
Keywords
oral squamous cell carcinoma
CXCR4
cisplatin
antitumor vascular therapy
Published Date
2024-06-25
Publication Title
Cancers
Volume
volume16
Issue
issue13
Publisher
MDPI
Start Page
2326
ISSN
2072-6694
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© 2024 by the authors.
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publisher
PubMed ID
DOI
Web of Science KeyUT
Related Url
isVersionOf https://doi.org/10.3390/cancers16132326
License
https://creativecommons.org/licenses/by/4.0/
Citation
Yoshida, S.; Kawai, H.; Soe, Y.; Eain, H.S.; Sanou, S.; Takabatake, K.; Takeshita, Y.; Hisatomi, M.; Nagatsuka, H.; Asaumi, J.; et al. Efficacy of Cisplatin–CXCR4 Antagonist Combination Therapy in Oral Cancer. Cancers 2024, 16, 2326. https://doi.org/10.3390/cancers16132326
Funder Name
Japan Society for the Promotion of Science
助成番号
19K19160
20H03888
23K09332
20K10178
23K09080
21K10043
22K10170
1K17089
23K16149
24K1313006
22KK027505