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人源抗体融合蛋白/抗体药物偶联物在乳腺癌和卵巢癌中的应用

Human Antibody Fusion Proteins/Antibody Drug Conjugates in Breast and Ovarian Cancer.

作者信息

Padayachee Eden R, Biteghe Fleury Augustin Nsole, Malindi Zaria, Bauerschlag Dirk, Barth Stefan

机构信息

Department of Integrative Biomedical Sciences, Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Department of Gynecological Oncology, University Medical Center Schleswig-Holstein, Campus Kiel, Christian-Albrechts University Kiel, Kiel, Germany.

出版信息

Transfus Med Hemother. 2017 Sep;44(5):303-310. doi: 10.1159/000479979. Epub 2017 Sep 11.

Abstract

Considerable research efforts have been dedicated to understanding ovarian and breast cancer mechanisms, but there has been little progress translating the research into effective clinical applications. Hence, personalized/precision medicine has emerged because of its potential to improve the accuracy of tumor targeting and minimize toxicity to normal tissue. Targeted therapy in both breast and ovarian cancer has focused on antibodies, antibody drug conjugates (ADCs), and very recently the introduction of human antibody fusion proteins. Small molecule inhibitors and monoclonal antibodies (mAbs) are used in conjunction with chemotherapeutic drugs as a form of treatment but problems arise from a board expression of the target antigen in healthy tissues. Also, insufficient tumor penetration due to tight binding affinity and macromolecular size of mAbs compromise the efficacy of these ADCs. A more targeted approach is thus needed, and ADCs were designed to meet this need. However, in ADCs the method of conjugation of drug to antibody is >1, altering the structure of the drug which leads to off-target effects. Random conjugation also causes the drug to affect the pharmokinetics and biodistribution of the antibody and may cause nonspecific binding and internalization. Recombinant therapeutic proteins achieve controlled conjugation reactions and combine cytotoxicity and targeting in one molecule. They can also be engineered to extend half-life, stability and mechanism of action, and offer novel delivery routes. SNAP-tag fusion proteins are an example of a theranostic recombinant protein as they provide a unique antibody format to conjugate a variety of benzyl guanine modified labels, e.g. fluorophores and photosensitizers in a 1:1 stoichiometry. On the one hand, SNAP tag fusions can be used to optically image tumors when conjugated to a fluorophore, and on the other hand the recombinant proteins can induce necrosis/apoptosis in the tumor when conjugated to a photosensitizer upon exposure to a changeable wavelength of light. The dual nature of SNAP-tag fusions as both a diagnostic and therapeutic tool reinforces its significant role in cancer treatment in an era of precision medicine.

摘要

大量的研究工作致力于了解卵巢癌和乳腺癌的发病机制,但在将研究成果转化为有效的临床应用方面进展甚微。因此,个性化/精准医学应运而生,因为它有可能提高肿瘤靶向的准确性,并将对正常组织的毒性降至最低。乳腺癌和卵巢癌的靶向治疗主要集中在抗体、抗体药物偶联物(ADC)上,最近还引入了人抗体融合蛋白。小分子抑制剂和单克隆抗体(mAb)与化疗药物联合使用作为一种治疗形式,但由于靶抗原在健康组织中的广泛表达而产生问题。此外,由于mAb的紧密结合亲和力和大分子尺寸导致肿瘤穿透不足,影响了这些ADC的疗效。因此需要一种更具针对性的方法,而ADC的设计正是为了满足这一需求。然而,在ADC中,药物与抗体的偶联方法不止一种,这会改变药物的结构,从而导致脱靶效应。随机偶联还会使药物影响抗体的药代动力学和生物分布,并可能导致非特异性结合和内化。重组治疗性蛋白实现了可控的偶联反应,并将细胞毒性和靶向性结合在一个分子中。它们还可以进行工程改造,以延长半衰期、稳定性和作用机制,并提供新的给药途径。SNAP-tag融合蛋白是一种治疗诊断性重组蛋白的例子,因为它们提供了一种独特的抗体形式,可以以1:1的化学计量比偶联各种苄基鸟嘌呤修饰的标记物,例如荧光团和光敏剂。一方面,SNAP标签融合物与荧光团偶联时可用于对肿瘤进行光学成像,另一方面,重组蛋白在暴露于可变波长的光下与光敏剂偶联时可诱导肿瘤坏死/凋亡。SNAP标签融合物作为诊断和治疗工具的双重性质,强化了其在精准医学时代癌症治疗中的重要作用。

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