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维甲酰胺 A 通过下调异常表达的紧密连接蛋白 1 减轻人口腔鳞癌细胞的转移表型。

Withaferin A mitigates metastatic traits in human oral squamous cell carcinoma caused by aberrant claudin-1 expression.

机构信息

Department of Oral Pathology, School of Dentistry and Dental Research Institute, Seoul National University, Seoul, 03080, Republic of Korea.

Department of Microbiology, Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul, 03722, Republic of Korea.

出版信息

Cell Biol Toxicol. 2022 Feb;38(1):147-165. doi: 10.1007/s10565-021-09584-2. Epub 2021 Mar 4.

DOI:10.1007/s10565-021-09584-2
PMID:33665778
Abstract

Abnormal expression of claudin-1 (CLDN1) has important roles in carcinogenesis and metastasis in various cancers. The role of CLDN1 in human oral squamous cell carcinoma (OSCC) remains unknown. Here, we report the functional role of CLDN1 in metastasis of human OSCC, as a potential target regulated by withaferin A. From gene expression profiling with microarray technology, we found that the majority of notable differentially expressed genes were classified into migration/invasion category. Withaferin A impaired the motility of human OSCC cells in vitro and suppressed metastatic nodule formation in an in vivo metastasis model, both associated with reduced CLDN1. CLDN1 overexpression enhanced metastatic nodule formation in vivo, resulting in severe metastatic lesions in lung tissue. Moreover, CLDN1 expression was positively correlated to lymphatic metastasis in OSCC patients. The impaired motility of human OSCC cells upon withaferin A treatment was restored by CLDN1 overexpression. Furthermore, upregulation of let-7a induced by withaferin A was inversely correlated to CLDN1 expression. Overall, these give us an insight into the function of CLDN1 for prognosis and treatment of human OSCC, substantiating further investigation into the use of withaferin A as good anti-metastatic drug candidate.

摘要

Claudin-1 (CLDN1) 的异常表达在各种癌症的发生和转移中起着重要作用。CLDN1 在人口腔鳞状细胞癌(OSCC)中的作用尚不清楚。在这里,我们报告了 CLDN1 在人 OSCC 转移中的功能作用,作为一个可能的靶点,受醉马草素 A 调节。通过微阵列技术的基因表达谱分析,我们发现大多数显著差异表达的基因被归类为迁移/侵袭类别。醉马草素 A 在体外损害人 OSCC 细胞的迁移能力,并抑制体内转移模型中的转移结节形成,均与 CLDN1 减少有关。CLDN1 的过表达增强了体内转移结节的形成,导致肺组织中严重的转移病变。此外,CLDN1 的表达与 OSCC 患者的淋巴转移呈正相关。醉马草素 A 处理后,人 OSCC 细胞迁移能力受损可通过 CLDN1 过表达恢复。此外,醉马草素 A 诱导的 let-7a 的上调与 CLDN1 的表达呈负相关。总的来说,这些结果为 CLDN1 作为人 OSCC 预后和治疗的功能提供了深入了解,进一步证实了醉马草素 A 作为一种良好的抗转移药物候选物的应用。

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