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TNBC Challenge: Oligonucleotide Aptamers for New Imaging and Therapy Modalities

机译:TNBC挑战:用于新型成像和治疗方式的寡核苷酸适体

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摘要

Compared to other breast cancers, triple-negative breast cancer (TNBC) usually affects younger patients, is larger in size, of higher grade and is biologically more aggressive. To date, conventional cytotoxic chemotherapy remains the only available treatment for TNBC because it lacks expression of the estrogen receptor (ER), progesterone receptor (PR) and epidermal growth factor receptor 2 (HER2), and no alternative targetable molecules have been identified so far. The high biological and clinical heterogeneity adds a further challenge to TNBC management and requires the identification of new biomarkers to improve detection by imaging, thus allowing the specific treatment of each individual TNBC subtype. The Systematic Evolution of Ligands by EXponential enrichment (SELEX) technique holds great promise to the search for novel targetable biomarkers, and aptamer-based molecular approaches have the potential to overcome obstacles of current imaging and therapy modalities. In this review, we highlight recent advances in oligonucleotide aptamers used as imaging and/or therapeutic agents in TNBC, discussing the potential options to discover, image and hit new actionable targets in TNBC.
机译:与其他乳腺癌相比,三阴性乳腺癌(TNBC)通常会影响年轻患者,其规模更大,等级更高并且在生物学上更具侵略性。迄今为止,常规的细胞毒性化学疗法仍然是TNBC唯一可用的治疗方法,因为它缺乏雌激素受体(ER),孕激素受体(PR)和表皮生长因子受体2(HER2)的表达,并且迄今为止尚未找到其他可靶向的分子。高度的生物学和临床异质性给TNBC管理带来了进一步的挑战,并要求鉴定新的生物标记物以通过成像改善检测,从而允许对每种单独的TNBC亚型进行特异性治疗。通过指数富集(SELEX)技术进行配体的系统进化对寻找新型可靶向生物标志物具有广阔的前景,基于适体的分子方法具有克服当前成像和治疗方式障碍的潜力。在这篇综述中,我们重点介绍了在TNBC中用作成像和/或治疗剂的寡核苷酸适体的最新进展,讨论了在TNBC中发现,成像和命中新的可操作靶标的潜在选择。

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