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肿瘤基质中的成纤维细胞产生的白血病抑制因子参与口腔鳞状细胞癌的侵袭。

Leukemia inhibitory factor produced by fibroblasts within tumor stroma participates in invasion of oral squamous cell carcinoma.

作者信息

Ohata Yae, Tsuchiya Maiko, Hirai Hideaki, Yamaguchi Satoshi, Akashi Takumi, Sakamoto Kei, Yamaguchi Akira, Ikeda Tohru, Kayamori Kou

机构信息

Department of Oral Pathology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.

Department of Oral and Maxillofacial Surgery, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.

出版信息

PLoS One. 2018 Feb 14;13(2):e0191865. doi: 10.1371/journal.pone.0191865. eCollection 2018.

Abstract

The interaction between cancer cells and the cancer stroma plays a crucial role in tumor progression and metastasis in diverse malignancies, including oral cancer. However, the mechanism underlying this interaction remains incompletely elucidated. Here, to investigate the interaction between oral cancer cells and fibroblasts, which are major cellular components of the tumor stroma, we conducted an in vitro study by using human oral squamous cell carcinoma (OSCC) cell lines and normal human dermal fibroblasts (NHDFs). The results of transwell assays revealed that the migration and invasion of 2 OSCC cell lines, HO1-N-1 and HSC3, were markedly stimulated upon coculturing with NHDFs. To investigate the factors that promote tumor invasion, we isolated NHDFs from cocultures prepared with HO1-N-1 cells and performed microarray analysis. Among the various genes that were upregulated, we identified the gene encoding leukemia inhibitory factor (LIF), and we focused on LIF in further analyses. We confirmed that all OSCC-derived conditioned media potently upregulated LIF expression in NHDFs, and the results of our transwell analysis demonstrated that NHDF-induced OSCC migration and invasion were inhibited by LIF-neutralizing antibodies. Furthermore, immunohistochemical analysis of patient samples revealed that in 44 out of 112 OSCC cases, LIF was expressed in the tumor stroma, particularly in cancer-associated fibroblasts (CAFs), and, notably, clinicopathological analyses confirmed that LIF expression in CAFs was significantly correlated with increased depth of tumor invasion. Collectively, our results suggest that OSCC stimulates fibroblasts to produce LIF, which, in turn, participates in cancer-cell invasion. Our finding offers a potential therapeutic strategy targeting the cancer stroma for the treatment of OSCC patients.

摘要

癌细胞与癌基质之间的相互作用在包括口腔癌在内的多种恶性肿瘤的肿瘤进展和转移中起着关键作用。然而,这种相互作用的潜在机制仍未完全阐明。在此,为了研究口腔癌细胞与作为肿瘤基质主要细胞成分的成纤维细胞之间的相互作用,我们使用人口腔鳞状细胞癌(OSCC)细胞系和正常人皮肤成纤维细胞(NHDFs)进行了一项体外研究。Transwell分析结果显示,与NHDFs共培养时,两种OSCC细胞系HO1-N-1和HSC3的迁移和侵袭受到显著刺激。为了研究促进肿瘤侵袭的因素,我们从与HO1-N-1细胞共培养制备的细胞中分离出NHDFs并进行了微阵列分析。在各种上调的基因中,我们鉴定出编码白血病抑制因子(LIF)的基因,并在进一步分析中聚焦于LIF。我们证实,所有源自OSCC的条件培养基均能有效上调NHDFs中LIF的表达,并且我们的Transwell分析结果表明,LIF中和抗体可抑制NHDF诱导的OSCC迁移和侵袭。此外,对患者样本的免疫组织化学分析显示,在112例OSCC病例中的44例中,LIF在肿瘤基质中表达,特别是在癌相关成纤维细胞(CAFs)中,并且值得注意的是,临床病理分析证实CAFs中LIF的表达与肿瘤侵袭深度增加显著相关。总体而言,我们的结果表明,OSCC刺激成纤维细胞产生LIF,而LIF反过来又参与癌细胞的侵袭。我们的发现为OSCC患者提供了一种针对癌基质的潜在治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6574/5812599/d54cc64876da/pone.0191865.g001.jpg

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