Establishment of an oral squamous cell carcinoma cell line expressing vascular endothelial growth factor a and its two receptors.

Establishment of an oral squamous cell carcinoma cell line expressing vascular endothelial growth factor a and its two receptors.
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表达血管内皮生长因子a及其两种受体的口腔鳞状细胞癌细胞系的建立。

DOI:
10.1016/j.jds.2022.04.018
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发表时间:
2022-10
影响因子:
3.5
通讯作者:
Kishimoto, Hiromitsu
Kishimoto, Hiromitsu
中科院分区:
医学4区
文献类型:
--
作者:
Araki-Maeda, Hanako;Kawabe, Mutsuki;Omori, Yuji;Yamanegi, Koji;Yoshida, Kazunari;Yoshikawa, Kyohei;Takaoka, Kazuki;Noguchi, Kazuma;Nakano, Yoshiro;Kishimoto, Hiromitsu

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血管内皮生长因子受体(VEGFR)在口腔鳞状细胞癌(OSCC)中的表达通过自分泌和旁分泌信号通路促进肿瘤生长。vegf阳性的OSCC病例与浸润深度高、转移增加和预后差有关。在这项研究中,我们建立了一种共表达VEGF-A、VEGFR-1和VEGFR-2的OSCC细胞系,称为HCM-SqCC010细胞,并对其进行了分子和功能分析。采用免疫组化和免疫印迹法检测HCM-SqCC010细胞中VEGF-A、VEGFR-1和VEGFR-2的表达。通过实时荧光定量PCR验证VEGF-A、VEGFR-1、VEGFR-2在HCM-SqCC010细胞中的表达及抑制作用。我们对HCM-SqCC010细胞的分析显示,它们的增殖依赖于VEGF-A,选择性抑制VEGFR-1或VEGFR-2导致细胞生长下降。我们建立了表达VEGF-A、VEGFR-1和VEGFR-2的OSCC细胞系HCM-SqCC010。这种三阳性细胞系对VEGF-A的分子靶向药物没有影响,但对VEGFR抑制剂的反应确实显示出强烈的细胞生长抑制。因此,针对OSCC的新治疗策略应该包括VEGFR抑制剂。
Vascular endothelial growth factor receptor (VEGFR) expression in oral squamous cell carcinoma (OSCC) promotes tumor growth through both autocrine and paracrine signaling. VEGF-positive OSCC cases are associated with a high depth of invasion, increased metastasis, and poor prognosis. In this study we established and then molecularly and functionally analyzed an OSCC cell line that co-expresses VEGF-A, VEGFR-1, and VEGFR-2, termed HCM-SqCC010 cells. VEGF-A, VEGFR-1, and VEGFR-2 expression in HCM-SqCC010 cells were examined by immunohistochemistry and immunoblotting. Expression and inhibition of VEGF-A, VEGFR-1, and VEGFR-2 in HCM-SqCC010 cells were verified by quantitative real-time PCR. Our analysis of HCM-SqCC010 cells revealed that their proliferation depended on VEGF-A, and selective inhibition of VEGFR-1 or VEGFR-2 resulted in decreased cell growth. We established an OSCC cell line, HCM-SqCC010, that expresses VEGF-A, VEGFR-1, and VEGFR-2. This triple-positive cell line showed no effect from a molecular targeted drug toward VEGF-A, but it did show strong cell growth inhibition in response to a VEGFR inhibitor. Thus, new therapeutic strategies against OSCC should include a VEGFR inhibitor.
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