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从食管梭形细胞癌建立的新型人类细胞系HN-Eso-1中的血管内皮生长因子及其受体

Vascular endothelial growth factors and their receptors in the novel human cell line, HN-Eso-1, established from esophageal spindle cell carcinoma.

作者信息

Nakatani Hajime, Akimori Toyokazu, Takezaki Yuka, Hanazaki Kazuhiro

机构信息

Department of Surgery, Kubokawa Hospital, Shimanto-cho, Kochi, Japan.

出版信息

J Med Invest. 2010 Aug;57(3-4):232-6. doi: 10.2152/jmi.57.232.

Abstract

Human carcinosarcomas of esophagus are uncommon malignant neoplasms that are composed both carcinomatous and sarcomatous components. We established a novel cell line, HN-Eso-1, from the metastatic esophageal spindle cell carcinoma (so-called carcinosarcoma). In this study, we estimated the vascular endothelial growth factors (VEGFs) and VEGF receptors (VEGFRs). Reverse transcription polymerase chain reaction (RT-PCR) studies revealed that VEGF-A, -C, -D and VEGFR-1, -2 were upregulated. Cisplatin reduced the cell viability of HN-Eso-1 cells and VEGF attenuated its effect. These results suggest that expression of VEGF-A, VEGF-C, VEGF-D, VEGFR-1, and VEGFR-2 are involved in the cell's autocrine system and that VEGF protected these cells from the anti-tumor agent.

摘要

食管人类癌肉瘤是一种罕见的恶性肿瘤,由癌性和肉瘤性成分组成。我们从转移性食管梭形细胞癌(所谓的癌肉瘤)中建立了一种新的细胞系HN-Eso-1。在本研究中,我们评估了血管内皮生长因子(VEGFs)和血管内皮生长因子受体(VEGFRs)。逆转录聚合酶链反应(RT-PCR)研究显示VEGF-A、-C、-D以及VEGFR-1、-2上调。顺铂降低了HN-Eso-1细胞的活力,而VEGF减弱了其作用。这些结果表明,VEGF-A、VEGF-C、VEGF-D、VEGFR-1和VEGFR-2的表达参与了细胞的自分泌系统,并且VEGF保护这些细胞免受抗肿瘤药物的影响。

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