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西妥昔单抗联合α-放射免疫疗法对培养的鳞状细胞癌的影响。

Effect of cetuximab in combination with alpha-radioimmunotherapy in cultured squamous cell carcinomas.

机构信息

Unit of Otolaryngology and Head & Neck Surgery, Department of Surgical Sciences, Uppsala University, S-751 85 Uppsala, Sweden.

出版信息

Nucl Med Biol. 2011 Jan;38(1):103-12. doi: 10.1016/j.nucmedbio.2010.06.014. Epub 2010 Aug 16.

Abstract

AIM

The monoclonal antibody cetuximab, targeting the epidermal growth factor receptor (EGFR), is a promising molecular targeting agent to be used in combination with radiation for anticancer therapy. In this study, effects of cetuximab in combination with alpha-emitting radioimmunotherapy (RIT) in a panel of cultured human squamous cell carcinomas (SCCs) were assessed.

METHODS

SCC cell lines were characterized and treated with cetuximab in combination with anti-CD44v6 RIT using the astatinated chimeric monoclonal antibody U36 ((211)At-cMAb U36). Effects on (211)At-cMAb U36 uptake, internalization and cell proliferation were then assessed in SCC cells.

RESULTS

Cetuximab in combination with (211)At-cMAb U36 mediated increased growth inhibition compared to RIT or cetuximab alone in two cell lines. However, cetuximab also mediated radioprotective effects compared to RIT alone in two cell lines. The radioprotective effects occurred in the cell lines in which cetuximab clearly inhibited cell growth during radiation exposure. Cetuximab treatment also influenced (211)At-cMAb-U36 uptake and internalization, suggesting interactions between CD44v6 and EGFR.

CONCLUSIONS

Results from this study demonstrate the vast importance of further clarifying the mechanisms of cetuximab and radiation response, and the relationship between EGFR and suitable RIT targets. This is important not only in order to avoid potential radioprotective effects, but also in order to find and utilize potential synergistic effects from these combinations.

摘要

目的

针对表皮生长因子受体(EGFR)的单克隆抗体西妥昔单抗是一种很有前途的分子靶向药物,可与放射治疗联合用于抗癌治疗。本研究评估了西妥昔单抗联合α发射放射性免疫治疗(RIT)在一系列培养的人鳞状细胞癌(SCC)中的作用。

方法

对 SCC 细胞系进行了特征描述,并使用放射性标记的嵌合单克隆抗体 U36([211]At-cMAb U36)联合西妥昔单抗进行了抗 CD44v6 RIT 治疗。然后,评估了 SCC 细胞中[211]At-cMAb U36 摄取、内化和细胞增殖的影响。

结果

与单独进行 RIT 或西妥昔单抗治疗相比,西妥昔单抗联合[211]At-cMAb U36 可在两种细胞系中介导更强的生长抑制作用。然而,与单独进行 RIT 相比,西妥昔单抗在两种细胞系中也介导了放射保护作用。放射保护作用发生在西妥昔单抗在辐射暴露期间明显抑制细胞生长的细胞系中。西妥昔单抗治疗还影响[211]At-cMAb-U36 的摄取和内化,表明 CD44v6 和 EGFR 之间存在相互作用。

结论

本研究结果表明,进一步阐明西妥昔单抗和放射反应的机制以及 EGFR 与合适的 RIT 靶标的关系非常重要。这不仅对于避免潜在的放射保护作用很重要,而且对于寻找和利用这些组合的潜在协同作用也很重要。

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