Maietta Immacolata, González-Fernández África, Simón-Vázquez Rosana
CINBIO, Universidade de Vigo, 36310 Vigo, Spain; Immunology Group, Galica Sur Health Research Institute (IIS-GS). SERGAS-UVIGO. Spain.
CINBIO, Universidade de Vigo, 36310 Vigo, Spain; Immunology Group, Galica Sur Health Research Institute (IIS-GS). SERGAS-UVIGO. Spain.
Adv Drug Deliv Rev. 2025 Jun 16;224:115638. doi: 10.1016/j.addr.2025.115638.
Pancreatic ductal adenocarcinoma (PDAC) is an aggressive and often fatal form of malignancy frequently diagnosed at an advanced stage, posing significant challenges for treatment. The complex and intricate microenvironment of PDAC, characterized by heterogenous tumoral cells harbouring diverse mutations and epigenetic alterations, immune cells (primarily in an immunosuppressive state), cancer-associated fibroblasts (CAFs), low vascularization and extracellular matrix components supporting tumor growth, creates a physical barrier that impedes drug delivery and anti-tumoral immune cell responses, leading to therapy resistance. Despite advancements in early detection methods, and available treatments for PDAC-including surgery, radiotherapy, chemotherapy, and immunotherapy, all have shown limited efficacy. Recently, liposomal drugs in combination therapy, PDAC-targeted CAR-T cells and anti-tumor RNA vaccines have emerged as promising therapeutic approaches. However, significant challenges remain, including the presence of a dense stroma, resistance to chemotherapy, and robust immune suppression, all of which pose substantial barriers to effective treatments. In this context, epigenetic therapy aims to modify gene expression patterns in PDAC cells, potentially curtailing their resistance. This review provides an overview of the current landscape of PDAC research and the role of epigenetic inhibitors in the treatment of this lethal disease, emphasizing the potential of combining these novel drugs with conventional chemotherapy or immunotherapy, new drug delivery approaches and future directions in the field. A multi-approach therapy, switch to simultaneously targeting various facets of the PDAC characteristics, could enhance the anti-tumoral efficacy by overcoming its resistance mechanisms, improving patient prognosis.
胰腺导管腺癌(PDAC)是一种侵袭性强且往往致命的恶性肿瘤,常在晚期被诊断出来,给治疗带来巨大挑战。PDAC复杂而精细的微环境具有以下特点:包含具有多种突变和表观遗传改变的异质性肿瘤细胞、免疫细胞(主要处于免疫抑制状态)、癌症相关成纤维细胞(CAFs)、低血管化以及支持肿瘤生长的细胞外基质成分,这些构成了一个物理屏障,阻碍药物递送和抗肿瘤免疫细胞反应,导致治疗耐药。尽管早期检测方法有所进步,且有多种针对PDAC的治疗方法,包括手术、放疗、化疗和免疫疗法,但所有这些方法的疗效都有限。最近,脂质体药物联合疗法、靶向PDAC的嵌合抗原受体T细胞(CAR-T)和抗肿瘤RNA疫苗已成为有前景的治疗方法。然而,仍存在重大挑战,包括致密基质的存在、对化疗的耐药性以及强大的免疫抑制,所有这些都对有效治疗构成了重大障碍。在这种背景下,表观遗传疗法旨在改变PDAC细胞中的基因表达模式,有可能减少其耐药性。本综述概述了PDAC研究的现状以及表观遗传抑制剂在治疗这种致命疾病中的作用,强调了将这些新型药物与传统化疗或免疫疗法、新的药物递送方法以及该领域未来方向相结合的潜力。一种多方法治疗,即同时针对PDAC特征的各个方面,通过克服其耐药机制,可能会提高抗肿瘤疗效,改善患者预后。