Leveraging epigenetics to enhance the efficacy of cancer-testis antigen: a potential candidate for immunotherapy

免疫疗法 癌症 卵巢癌 癌症研究 生物 癌症免疫疗法 T细胞 树突状细胞 恶性肿瘤 抗原 免疫学 伏立诺他 免疫系统 组蛋白脱乙酰基酶 组蛋白 基因 生物化学 遗传学
作者
Ramji Gupta,Bimal Prasad Jit,Santosh Kumar,Sandeep Mittan,Pranay Tanwer,Mukurdipi Ray,Sandeep Mathur,Vanamail Perumal,Lalit Kumar,GK Rath,Ashok Sharma
出处
期刊:Epigenomics [Future Medicine]
卷期号:14 (14): 865-886
标识
DOI:10.2217/epi-2021-0479
摘要

Ovarian cancer is the most lethal gynecological malignancy in women. The phenotype is characterized by delayed diagnosis, recurrence and drug resistance. Inherent immunogenicity potential, oncogenic function and expression of cancer-testis/germline antigen (CTA) in ovarian cancer render them a potential candidate for immunotherapy. Revolutionary clinical findings indicate that tumor antigen-mediated T-cell and dendritic cell-based immunotherapeutic approaches provide an excellent strategy for targeting tumors. Currently, dendritic cell vaccination for the treatment of B-cell lymphoma and CTA-based T-cell receptor transduced T-cell therapy involving MAGE-A4 and NY-ESO-1 are well documented and shown to be effective. This review highlighted the mechanical aspects of epigenetic drugs that can elicit a CTA-based humoral and cellular immune response and implicate T-cell and dendritic cell-based immunotherapeutic approaches.Despite substantial advancements in prognosis and diagnostic approaches, epithelial ovarian cancer is still the most lethal gynecological malignancy worldwide. In addition to radiotherapy, chemotherapy, hormonal therapy, and surgery, immunotherapy in the clinical setting is promising. Tumor-restricted expression and strong immunogenic potential make cancer-testis/germline antigen (CTA) a potential candidate for efficient T-cell and dendritic cell-mediated cancer immunotherapy. The expression of CTAs is shown to be modulated by a specific epigenetic fine-tuning mechanism. However, the expression and role of CTA in epithelial ovarian cancer immunotherapy are poorly understood. Therefore, in the current work, the authors thoroughly highlight and explore the possible epigenetic mechanisms associated with CTA expression and their implication in T-cell and dendritic cell-based immunotherapy approaches to ovarian cancer. Understanding such a paradigm is essential to adopting a precision medicine approach for better therapeutic options.
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