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首页> 外文期刊>American Journal of Cancer Research >Radiation-induced tumor neoantigens: imaging and therapeutic implications
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Radiation-induced tumor neoantigens: imaging and therapeutic implications

机译:辐射诱导的肿瘤新抗原:成像和治疗意义

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摘要

Exposure of tumor cells to ionizing radiation (IR) is widely known to induce a number of cellular changes. One way that IR can affect tumor cells is through the development of neoantigens which are new molecules that tumor cells express at the cell membrane following some insult or change to the cell. There have been numerous reports in the literature of changes in both tumor and tumor vasculature cell surface molecule expression following treatment with IR. The usefulness of neoantigens for imaging and therapeutic applications lies in the fact that they are differentially expressed on the surface of irradiated tumor cells to a greater extent than on normal tissues. This differential expression provides a mechanism by which tumor cells can be “marked” by radiation for further targeting. Drug delivery vehicles or imaging agents conjugated to ligands that recognize and interact with the neoantigens can help to improve tumor-specific targeting and reduce systemic toxicity with cancer drugs. This article provides a review of the molecules that have been reported to be expressed on the surface of tumor cells in response to IR either in vivo or in vitro. Additionally, we provide a discussion of some of the methods used in the identification of these antigens and applications for their use in drug delivery and imaging.
机译:众所周知,将肿瘤细胞暴露于电离辐射(IR)会诱导许多细胞变化。 IR可以影响肿瘤细胞的一种方式是通过开发新抗原,这些新抗原是肿瘤细胞在受到某种侮辱或改变后在细胞膜上表达的新分子。用IR治疗后,肿瘤和肿瘤脉管系统细胞表面分子表达的变化在文献中已有许多报道。新抗原在成像和治疗应用中的有用性在于,它们在被照射的肿瘤细胞表面上的差异表达要比在正常组织上更大。这种差异表达提供了一种机制,通过该机制肿瘤细胞可以被辐射“标记”以进一步靶向。与识别并与新抗原相互作用的配体上缀合的药物输送媒介或成像剂可帮助改善肿瘤特异性靶向并降低癌症药物的全身毒性。本文综述了已报道在体内或体外对IR响应的肿瘤细胞表面表达的分子。此外,我们提供了一些用于鉴定这些抗原的方法及其在药物递送和成像中的应用的讨论。

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