EphA4 signaling is involved in the phenotype of well-differentiated oral squamous cell arcinoma with decreased tumor immunity

Metronomic chemotherapy is defined as a high-frequency low-dose schedule of chemotherapy drug administration. Although metronomic chemotherapy is widely used, the mechanisms underlying resistance to metronomic chemotherapy remain unclear. Therefore, we herein conducted a single institutional phase I...

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Veröffentlicht in:European journal of pharmacology 2023-04, Vol.945, p.175611-175611, Article 175611
Hauptverfasser: Kina, Shinichiro, Kawabata-Iwakawa, Reika, Miyamoto, Sho, Kato, Tomoki, Kina-Tanada, Mika, Arasaki, Akira
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container_title European journal of pharmacology
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creator Kina, Shinichiro
Kawabata-Iwakawa, Reika
Miyamoto, Sho
Kato, Tomoki
Kina-Tanada, Mika
Arasaki, Akira
description Metronomic chemotherapy is defined as a high-frequency low-dose schedule of chemotherapy drug administration. Although metronomic chemotherapy is widely used, the mechanisms underlying resistance to metronomic chemotherapy remain unclear. Therefore, we herein conducted a single institutional phase I/II trial to assess the efficacy and safety of metronomic chemotherapy with bleomycin plus S-1, an oral 5-FU prodrug, in the neoadjuvant setting for patients with oral squamous cell carcinoma (OSCC). The response rate of well-differentiated OSCC to metronomic chemotherapy was significantly lower. We investigated differences in molecular profiles between poorly or moderately differentiated head and neck squamous cell carcinoma (HNSCC) and well-differentiated HNSCC from patients with HNSCC TCGA data. EphA4 expression positively correlated with histological differentiation. An upstream regulator analysis correlated with EphA4 expression identified pathways associated with decreased mTORC1 signaling and T cell activation, including TCR, CD3, CD28, and CD40LG. An EphA4 blocking peptide (KYL) induced mTOR activation in well-differentiated OSCC cell lines. Plasmacytoid dendritic cell and CD8+ T cell numbers were higher in the microenvironment of poorly or moderately differentiated HNSCC than in that of well-differentiated HNSCC. Well-differentiated HNSCC had the characteristics of “cold tumors” (immune-excluded tumors). Moreover, KYL used with chemotherapeutic drugs synergistically increased cancer cell death. Well-differentiated OSCC is depleted of immune cells, which may be partly explained by the receptor tyrosine kinase EphA4. [Display omitted] •Well-differentiated OSCC had significantly lower response rates to metronomic chemotherapy.•HNSCC patients with well differentiation have higher expression of EphA4.•EphA4 inhibited mTOR activation in OSCC cell lines.•HNSCC with high EphA4 expression reveals immune excluded tumors characteristics.•Well-differentiated HNSCC reveals immune excluded tumors characteristics.
doi_str_mv 10.1016/j.ejphar.2023.175611
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Although metronomic chemotherapy is widely used, the mechanisms underlying resistance to metronomic chemotherapy remain unclear. Therefore, we herein conducted a single institutional phase I/II trial to assess the efficacy and safety of metronomic chemotherapy with bleomycin plus S-1, an oral 5-FU prodrug, in the neoadjuvant setting for patients with oral squamous cell carcinoma (OSCC). The response rate of well-differentiated OSCC to metronomic chemotherapy was significantly lower. We investigated differences in molecular profiles between poorly or moderately differentiated head and neck squamous cell carcinoma (HNSCC) and well-differentiated HNSCC from patients with HNSCC TCGA data. EphA4 expression positively correlated with histological differentiation. An upstream regulator analysis correlated with EphA4 expression identified pathways associated with decreased mTORC1 signaling and T cell activation, including TCR, CD3, CD28, and CD40LG. An EphA4 blocking peptide (KYL) induced mTOR activation in well-differentiated OSCC cell lines. Plasmacytoid dendritic cell and CD8+ T cell numbers were higher in the microenvironment of poorly or moderately differentiated HNSCC than in that of well-differentiated HNSCC. Well-differentiated HNSCC had the characteristics of “cold tumors” (immune-excluded tumors). Moreover, KYL used with chemotherapeutic drugs synergistically increased cancer cell death. Well-differentiated OSCC is depleted of immune cells, which may be partly explained by the receptor tyrosine kinase EphA4. [Display omitted] •Well-differentiated OSCC had significantly lower response rates to metronomic chemotherapy.•HNSCC patients with well differentiation have higher expression of EphA4.•EphA4 inhibited mTOR activation in OSCC cell lines.•HNSCC with high EphA4 expression reveals immune excluded tumors characteristics.•Well-differentiated HNSCC reveals immune excluded tumors characteristics.</description><identifier>ISSN: 0014-2999</identifier><identifier>EISSN: 1879-0712</identifier><identifier>DOI: 10.1016/j.ejphar.2023.175611</identifier><identifier>PMID: 36804938</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Carcinoma, Squamous Cell - drug therapy ; Carcinoma, Squamous Cell - metabolism ; Epithelial Cells - metabolism ; Head and Neck Neoplasms - drug therapy ; Humans ; Mouth Neoplasms - metabolism ; Phenotype ; Receptor, EphA4 - metabolism ; Squamous Cell Carcinoma of Head and Neck - drug therapy ; Tumor Microenvironment</subject><ispartof>European journal of pharmacology, 2023-04, Vol.945, p.175611-175611, Article 175611</ispartof><rights>2023 The Authors</rights><rights>Copyright © 2023 The Authors. 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An EphA4 blocking peptide (KYL) induced mTOR activation in well-differentiated OSCC cell lines. Plasmacytoid dendritic cell and CD8+ T cell numbers were higher in the microenvironment of poorly or moderately differentiated HNSCC than in that of well-differentiated HNSCC. Well-differentiated HNSCC had the characteristics of “cold tumors” (immune-excluded tumors). Moreover, KYL used with chemotherapeutic drugs synergistically increased cancer cell death. Well-differentiated OSCC is depleted of immune cells, which may be partly explained by the receptor tyrosine kinase EphA4. 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An EphA4 blocking peptide (KYL) induced mTOR activation in well-differentiated OSCC cell lines. Plasmacytoid dendritic cell and CD8+ T cell numbers were higher in the microenvironment of poorly or moderately differentiated HNSCC than in that of well-differentiated HNSCC. Well-differentiated HNSCC had the characteristics of “cold tumors” (immune-excluded tumors). Moreover, KYL used with chemotherapeutic drugs synergistically increased cancer cell death. Well-differentiated OSCC is depleted of immune cells, which may be partly explained by the receptor tyrosine kinase EphA4. 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subjects Carcinoma, Squamous Cell - drug therapy
Carcinoma, Squamous Cell - metabolism
Epithelial Cells - metabolism
Head and Neck Neoplasms - drug therapy
Humans
Mouth Neoplasms - metabolism
Phenotype
Receptor, EphA4 - metabolism
Squamous Cell Carcinoma of Head and Neck - drug therapy
Tumor Microenvironment
title EphA4 signaling is involved in the phenotype of well-differentiated oral squamous cell arcinoma with decreased tumor immunity
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