Zuhair Chaudhry, Anik Boyadzhyan, Kayvan Sasaninia, Vikant Rai
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Previously, researchers have been able to utilize these immunogenic properties and manufacture neoantigen-specific T-cells and neoantigen vaccines. Within the context of breast cancer, biomarkers such as tumor protein 53 (TP53), Survivin, Partner and Localizer of BRCA2 (PALB2), and protein tyrosine phosphatase receptor T (PTPRT) display exceeding potential to serve as neoantigens. However, despite their seemingly limitless potential, neoantigens must overcome various obstacles if they are to be fairly distributed to patients. For instance, a prolonged period between the identification of a neoantigen and the dispersal of treatment poses a serious risk within the context of breast cancer. Regardless of these current obstacles, it appears highly promising that future research into neoantigens will make an everlasting impact on the health outcomes within the realm of breast cancer. 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引用次数: 0
摘要
作为全球发病率最高的癌症之一,乳腺癌在临床研究领域备受关注。传统治疗采用多学科方法,包括化疗、激素治疗甚至手术等多种疗法,而研究人员则开始关注新抗原的萌芽作用。新抗原被定义为肿瘤特异性抗原,由多种基因改变产生,其中最常见的是单核苷酸变异。由于其外来性质,新抗原会在主要组织相容性复合物 I 和 II 呈递后引起免疫反应,然后被 T 细胞受体识别。此前,研究人员已经能够利用这些免疫原性制造新抗原特异性 T 细胞和新抗原疫苗。在乳腺癌方面,肿瘤蛋白 53 (TP53)、Survivin、BRCA2 的伙伴和定位器 (PALB2) 以及蛋白酪氨酸磷酸酶受体 T (PTPRT) 等生物标记物显示出作为新抗原的巨大潜力。然而,尽管新抗原看似潜力无限,但要想公平地分配给患者,还必须克服各种障碍。例如,在乳腺癌的治疗过程中,新抗原的确定与治疗分散之间的时间间隔过长就会带来严重的风险。尽管目前存在这些障碍,但未来对新抗原的研究将对乳腺癌领域的健康结果产生持久的影响,这似乎是大有希望的。本文献综述的目的是全面讨论各种形式乳腺癌的病因和当前的治疗方法,然后讨论新抗原在癌症治疗中的意义及其在乳腺癌中的应用。此外,我们还讨论了转录组学在新抗原识别和个性化医疗中的局限性、未来方向和作用。原始文章和综述文章中讨论的概念已纳入本综述文章。
Targeting Neoantigens in Cancer: Possibilities and Opportunities in Breast Cancer
As one of the most prevalent forms of cancer worldwide, breast cancer has garnered significant attention within the clinical research setting. While traditional treatment employs a multidisciplinary approach including a variety of therapies such as chemotherapy, hormone therapy, and even surgery, researchers have since directed their attention to the budding role of neoantigens. Neoantigens are defined as tumor-specific antigens that result from a multitude of genetic alterations, the most prevalent of which is the single nucleotide variant. As a result of their foreign nature, neoantigens elicit immune responses upon presentation by Major Histocompatibility Complexes I and II followed by recognition by T cell receptors. Previously, researchers have been able to utilize these immunogenic properties and manufacture neoantigen-specific T-cells and neoantigen vaccines. Within the context of breast cancer, biomarkers such as tumor protein 53 (TP53), Survivin, Partner and Localizer of BRCA2 (PALB2), and protein tyrosine phosphatase receptor T (PTPRT) display exceeding potential to serve as neoantigens. However, despite their seemingly limitless potential, neoantigens must overcome various obstacles if they are to be fairly distributed to patients. For instance, a prolonged period between the identification of a neoantigen and the dispersal of treatment poses a serious risk within the context of breast cancer. Regardless of these current obstacles, it appears highly promising that future research into neoantigens will make an everlasting impact on the health outcomes within the realm of breast cancer. The purpose of this literature review is to comprehensively discuss the etiology of various forms of breast cancer and current treatment modalities followed by the significance of neoantigens in cancer therapeutics and their application to breast cancer. Further, we have discussed the limitations, future directions, and the role of transcriptomics in neoantigen identification and personalized medicine. The concepts discussed in the original and review articles were included in this review article.
期刊介绍:
Antibodies (ISSN 2073-4468), an international, peer-reviewed open access journal which provides an advanced forum for studies related to antibodies and antigens. It publishes reviews, research articles, communications and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. Full experimental and/or methodical details must be provided. Electronic files or software regarding the full details of the calculation and experimental procedure - if unable to be published in a normal way - can be deposited as supplementary material. This journal covers all topics related to antibodies and antigens, topics of interest include (but are not limited to): antibody-producing cells (including B cells), antibody structure and function, antibody-antigen interactions, Fc receptors, antibody manufacturing antibody engineering, antibody therapy, immunoassays, antibody diagnosis, tissue antigens, exogenous antigens, endogenous antigens, autoantigens, monoclonal antibodies, natural antibodies, humoral immune responses, immunoregulatory molecules.