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Effects of CRM197, a specific inhibitor of HB-EGF, in oral cancer

机译:CRM197,HB-EGF的特异性抑制剂,在口腔癌中的作用

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CRM197, a nontoxic mutant of diphtheria toxin, is a specific inhibitor of heparin-binding epidermal growth factor (EGF)-like growth factor (HB-EGF), which belongs to the EGF family that has been implicated in the increased progression, proliferation, and metastasis of oral cancer. In this study, we analyzed the antitumor effects of CRM197, which represent possible chemotherapeutic agents for oral cancer. In the experiment, we used the oral squamous cell carcinoma cell lines HSC3 and SAS. Cells treated with CRM197 were analyzed based on cell viability, MTT assay, invasion assay, Western blot, and zymography. HSC3 cells were injected subcutaneously into female BALB/c nuu mice at 5 weeks of age. CRM197 and/or CDDP were injected intraperitoneally into tumor-bearing mice, and tumor volume was measured over time. HB-EGF expression in HSC3 and SAS cells treated with CRM197 was significantly reduced and cell proliferation was inhibited. The invasiveness of CRM197-treated cells was relatively low. MMP-9 and VEGF were suppressed in HSC3 treated with CRM197 on zymography and Western blot. Further, tumor growth in xenografted mice was suppressed by CRM197 or CDDP at 1 mg/kg/day. Also, the coadministra-tion of CDDP and CRM197 at 1 mg/kg/day completely inhibited tumor formation. These results suggest that HB-EGF is a target for oral cancer and that CRM197 is effective in oral cancer therapy.
机译:CRM197是白喉毒素的一种无毒突变体,是肝素结合表皮生长因子(EGF)样生长因子(HB-EGF)的特异性抑制剂,属于EGF家族,参与了增加的进展,增殖,和口腔癌的转移。在这项研究中,我们分析了CRM197的抗肿瘤作用,CRM197可能是口腔癌的化学治疗剂。在实验中,我们使用了口腔鳞状细胞癌细胞系HSC3和SAS。基于细胞活力,MTT测定,侵袭测定,蛋白质印迹和酶谱分析用CRM197处理的细胞。将HSC3细胞皮下注射到5周龄的雌性BALB / c nu / nu小鼠中。将CRM197和/或CDDP腹膜内注射到荷瘤小鼠中,并随时间测量肿瘤体积。 CRM197处理的HSC3和SAS细胞中的HB-EGF表达明显降低,并且细胞增殖受到抑制。 CRM197处理的细胞的侵袭性相对较低。通过酶谱和Western印迹,在用CRM197处理的HSC3中,MMP-9和VEGF被抑制。此外,CRM197或CDDP以1 mg / kg /天抑制异种移植小鼠的肿瘤生长。同样,以1 mg / kg /天的CDDP和CRM197的共同给药完全抑制了肿瘤的形成。这些结果表明HB-EGF是口腔癌的靶标,并且CRM197在口腔癌治疗中是有效的。

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