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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Effects of Maackia amurensis seed lectin (MASL) on oral squamous cell carcinoma (OSCC) gene expression and transcriptional signaling pathways
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Effects of Maackia amurensis seed lectin (MASL) on oral squamous cell carcinoma (OSCC) gene expression and transcriptional signaling pathways

机译:Maackia Amurensis Sercin(MasL)对口腔鳞状细胞癌(OSCC)基因表达和转录信号通路的影响

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Purpose Oral cancer causes over 120,000 deaths annually and affects the quality of life for survivors. Over 90% of oral cancers are derived from oral squamous cell carcinoma cells (OSCCs) which are generally resistant to standard cytotoxic chemotherapy agents. OSCC cells often exhibit increased TGF beta and PDPN receptor activity compared to nontransformed oral epithelial cells. Maackia amurensis seed lectin (MASL) can target the PDPN receptor and has been identified as a novel agent that can be used to treat oral cancer. However, mechanisms by which MASL inhibits OSCC progression are not yet clearly defined. Methods Here, we performed cell migration and cytotoxicity assays to assess the effects of MASL on OSCC motility and viability at physiologically relevant concentrations. We then performed comprehensive transcriptome analysis combined with transcription factor reporter assays to investigate the how MASL affects OSCC gene expression at these concentration. Key data were then confirmed by western blotting to evaluate the effects of MASL on gene expression and kinase signaling activity at the protein level. Results MASL significantly affected the expression of about 27% of approximately 15,000 genes found to be expressed by HSC-2 cells used to model OSCC cells in this study. These genes affected by MASL include members of the TGF beta-SMAD, JAK-STAT, and Wnt-beta CTN signaling pathways. In particular, MASL decreased expression of PDPN, SOX2, and SMAD5 at the RNA and protein levels. MASL also inhibited SMAD and MAPK activity, and exhibited potential for combination therapy with doxorubicin and 5-fluorouracil. Conclusions Taken together, results from this study indicate that MASL decreases activity of JAK-STAT, TGF beta-SMAD, and Wnt-beta CTN signaling pathways to inhibit OSCC growth and motility. These data suggest that further studies should be undertaken to determine how MASL may also be used alone and in combination with other agents to treat oral cancer.
机译:目的口腔癌每年造成超过12万人死亡,并影响幸存者的生活质量。超过90%的口腔癌源于口腔鳞状细胞癌细胞(OSCC),它们通常对标准的细胞毒性化疗药物具有耐药性。与未转化的口腔上皮细胞相比,口腔鳞癌细胞的TGF-β和PDPN受体活性通常增加。马钱子种子凝集素(MASL)可以靶向PDPN受体,已被确定为一种可用于治疗口腔癌的新型药物。然而,MASL抑制OSCC进展的机制尚不明确。方法在这里,我们进行细胞迁移和细胞毒性试验,以评估在生理相关浓度下MASL对OSCC运动性和活力的影响。然后,我们进行了综合转录组分析和转录因子报告分析,以研究MASL在这些浓度下如何影响OSCC基因表达。然后通过western blotting确认关键数据,以评估MASL在蛋白质水平上对基因表达和激酶信号活性的影响。结果在本研究中,用于模拟OSCC细胞的HSC-2细胞发现,MASL显著影响约15000个基因中约27%的基因的表达。这些受MASL影响的基因包括TGFβSMAD、JAK-STAT和WntβCTN信号通路的成员。特别是,MASL在RNA和蛋白质水平上降低了PDPN、SOX2和SMAD5的表达。MASL还抑制SMAD和MAPK活性,并显示出与阿霉素和5-氟尿嘧啶联合治疗的潜力。结论综上所述,本研究结果表明MASL降低JAK-STAT、TGF-β-SMAD和Wnt-β-CTN信号通路的活性,从而抑制OSCC的生长和运动。这些数据表明,应该进行进一步的研究,以确定MASL如何单独使用以及与其他药物联合使用来治疗口腔癌。

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