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靶向 HER2 乳腺癌的诊断与治疗:一种新方法。

Diagnostics and Therapeutics in Targeting HER2 Breast Cancer: A Novel Approach.

机构信息

School of Medicine, Deakin University, Geelong, VIC 3220, Australia.

Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Deakin University, Geelong, VIC 3220, Australia.

出版信息

Int J Mol Sci. 2021 Jun 7;22(11):6163. doi: 10.3390/ijms22116163.

DOI:10.3390/ijms22116163
PMID:34200484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8201268/
Abstract

Breast cancer is one of the most commonly occurring cancers in women globally and is the primary cause of cancer mortality in females. BC is highly heterogeneous with various phenotypic expressions. The overexpression of HER2 is responsible for 15-30% of all invasive BC and is strongly associated with malignant behaviours, poor prognosis and decline in overall survival. Molecular imaging offers advantages over conventional imaging modalities, as it provides more sensitive and specific detection of tumours, as these techniques measure the biological and physiological processes at the cellular level to visualise the disease. Early detection and diagnosis of BC is crucial to improving clinical outcomes and prognosis. While HER2-specific antibodies and nanobodies may improve the sensitivity and specificity of molecular imaging, the radioisotope conjugation process may interfere with and may compromise their binding functionalities. Aptamers are single-stranded oligonucleotides capable of targeting biomarkers with remarkable binding specificity and affinity. Aptamers can be functionalised with radioisotopes without compromising target specificity. The attachment of different radioisotopes can determine the aptamer's functionality in the treatment of HER2(+) BC. Several HER2 aptamers and investigations of them have been described and evaluated in this paper. We also provide recommendations for future studies with HER2 aptamers to target HER2(+) BC.

摘要

乳腺癌是全球女性最常见的癌症之一,也是女性癌症死亡的主要原因。乳腺癌具有高度异质性,表现出各种表型。HER2 的过表达负责所有浸润性乳腺癌的 15-30%,与恶性行为、不良预后和总生存下降密切相关。分子成像优于传统成像方式,因为它能够更敏感、更特异地检测肿瘤,因为这些技术可以测量细胞水平的生物和生理过程,从而可视化疾病。早期发现和诊断乳腺癌对于改善临床结果和预后至关重要。虽然 HER2 特异性抗体和纳米抗体可以提高分子成像的灵敏度和特异性,但放射性同位素缀合过程可能会干扰并可能损害它们的结合功能。适体是能够与生物标志物具有显著结合特异性和亲和力的单链寡核苷酸。适体可以与放射性同位素结合而不损害靶特异性。不同放射性同位素的附着可以决定适体在治疗 HER2(+)乳腺癌中的功能。本文描述和评估了几种 HER2 适体及其研究。我们还为未来针对 HER2(+)乳腺癌的 HER2 适体研究提供了建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6e1/8201268/9b64793956c5/ijms-22-06163-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6e1/8201268/9b64793956c5/ijms-22-06163-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6e1/8201268/9b64793956c5/ijms-22-06163-g001.jpg

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Radiopharmaceutical therapy in cancer: clinical advances and challenges.放射性药物治疗癌症:临床进展与挑战。
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