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干扰素诱导跨膜蛋白 1(IFITM1)促进小细胞肺癌的远处转移。

Interferon-Induced Transmembrane Protein 1 (IFITM1) Promotes Distant Metastasis of Small Cell Lung Cancer.

机构信息

Institute of Microbial Chemistry (BIKAKEN), Numazu, Microbial Chemistry Research Foundation, 18-24 Miyamoto, Numazu 410-0301, Japan.

Institute of Microbial Chemistry (BIKAKEN), Laboratory of Virology, Microbial Chemistry Research Foundation, 3-14-23 Kamiosaki, Shinagawa, Tokyo 141-0021, Japan.

出版信息

Int J Mol Sci. 2020 Jul 13;21(14):4934. doi: 10.3390/ijms21144934.

Abstract

Small cell lung cancer (SCLC) is a severe malignancy associated with early and widespread metastasis. To study SCLC metastasis, we previously developed an orthotopic transplantation model using the human SCLC cell line DMS273. In the model, metastatic foci were found in distant tissues such as bone and the adrenal gland, similarly as observed in patients with SCLC. In this study, we evaluated the differentially expressed genes between orthotopic and metastatic tumors in the model. We isolated tumor cells from orthotopic and metastatic sites, and the tumor cell RNA was analyzed using DNA microarray analysis. We found that 19 genes in metastatic tumors were upregulated by more than 4-fold compared with their expression in orthotopic tumors. One of these genes encodes a transmembrane protein, interferon (IFN)-induced transmembrane protein 1 (IFITM1), and immunohistochemical analysis confirmed the higher expression of the protein in metastatic sites than in orthotopic sites. IFITM1 was also detected in some SCLC cell lines and lung tumors from patients with SCLC. The overexpression of IFITM1 in DMS273 cells increased their metastatic formation in the orthotopic model and in an experimental metastasis model. Conversely, the silencing of IFITM1 suppressed metastatic formation by DMS273 cells. We also found that IFITM1 overexpression promoted the metastatic formation of NCI-H69 human SCLC cells. These results demonstrate that IFITM1 promotes distant metastasis in xenograft models of human SCLC.

摘要

小细胞肺癌(SCLC)是一种严重的恶性肿瘤,具有早期广泛转移的特点。为了研究 SCLC 的转移,我们之前使用人 SCLC 细胞系 DMS273 建立了一种原位移植模型。在该模型中,在骨骼和肾上腺等远处组织中发现了转移灶,与 SCLC 患者的观察结果相似。在这项研究中,我们评估了模型中原位和转移肿瘤之间差异表达的基因。我们从原位和转移部位分离肿瘤细胞,并使用 DNA 微阵列分析对肿瘤细胞 RNA 进行分析。我们发现,与原位肿瘤相比,转移肿瘤中有 19 个基因的表达上调了 4 倍以上。其中一个基因编码一种跨膜蛋白,干扰素(IFN)诱导的跨膜蛋白 1(IFITM1),免疫组织化学分析证实该蛋白在转移部位的表达高于原位部位。IFITM1 也在一些 SCLC 细胞系和 SCLC 患者的肺肿瘤中被检测到。在 DMS273 细胞中过表达 IFITM1 增加了其在原位模型和实验性转移模型中的转移形成。相反,IFITM1 的沉默抑制了 DMS273 细胞的转移形成。我们还发现 IFITM1 过表达促进了 NCI-H69 人 SCLC 细胞的转移形成。这些结果表明 IFITM1 促进了人 SCLC 异种移植模型中的远处转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73b1/7404048/ae7cfa7c1036/ijms-21-04934-g001.jpg

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