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CD147-亲环素 A 相互作用促进皮肤 T 细胞淋巴瘤的增殖和存活。

CD147-Cyclophilin a Interactions Promote Proliferation and Survival of Cutaneous T-Cell Lymphoma.

机构信息

Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo 113-8655, Japan.

Department of Dermatology, St. Marianna University School of Medicine, Kanagawa 216-8511, Japan.

出版信息

Int J Mol Sci. 2021 Jul 23;22(15):7889. doi: 10.3390/ijms22157889.

Abstract

CD147, a transmembrane glycoprotein that belongs to the immunoglobulin superfamily, and cyclophilin A (CypA), one of the binding partners of CD147, are overexpressed in tumor cells and associated with the progression of several malignancies, including both solid and hematological malignancies. However, CD147 and CypA involvement in cutaneous T-cell lymphoma (CTCL) has not been reported. In this study, we examined CD147 and CypA expression and function using clinical samples of mycosis fungoides (MF) and Sézary syndrome (SS) and CTCL cell lines. CD147 and CypA were overexpressed by tumor cells of MF/SS, and CypA was also expressed by epidermal keratinocytes in MF/SS lesional skin. Serum CypA levels were increased and correlated with disease severity markers in MF/SS patients. Anti-CD147 antibody and/or anti-CypA antibody suppressed the proliferation of CTCL cell lines, both in vitro and in vivo, via downregulation of phosphorylated extracellular-regulated kinase 1/2 and Akt. These results suggest that CD147-CypA interactions can contribute to the proliferation of MF/SS tumor cells in both a autocrine and paracrine manner, and that the disruption of CD147-CypA interactions could be a new therapeutic strategy for the treatment of MF/SS.

摘要

CD147 是一种跨膜糖蛋白,属于免疫球蛋白超家族,其结合伴侣之一的亲环素 A(CypA)在肿瘤细胞中过度表达,并与多种恶性肿瘤的进展相关,包括实体瘤和血液恶性肿瘤。然而,CD147 和 CypA 参与皮肤 T 细胞淋巴瘤(CTCL)尚未见报道。在这项研究中,我们使用蕈样肉芽肿(MF)和 Sézary 综合征(SS)以及 CTCL 细胞系的临床样本检查了 CD147 和 CypA 的表达和功能。MF/SS 的肿瘤细胞过度表达 CD147 和 CypA,并且 CypA 也在 MF/SS 病变皮肤的表皮角质形成细胞中表达。MF/SS 患者的血清 CypA 水平升高,并与疾病严重程度标志物相关。抗 CD147 抗体和/或抗 CypA 抗体通过下调磷酸化细胞外调节激酶 1/2 和 Akt,在体外和体内均抑制 CTCL 细胞系的增殖。这些结果表明,CD147-CypA 相互作用可以通过自分泌和旁分泌的方式促进 MF/SS 肿瘤细胞的增殖,并且破坏 CD147-CypA 相互作用可能是治疗 MF/SS 的一种新的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5633/8346093/6703a983ce62/ijms-22-07889-g001.jpg

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