Zekavat Lily, Jain Aditi
Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Jefferson Pancreas, Biliary and Related Cancer Center, Department of Surgery, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Int J Mol Sci. 2025 Sep 17;26(18):9041. doi: 10.3390/ijms26189041.
Pancreatic ductal adenocarcinoma (PDAC) is an aggressive solid malignancy with poor overall prognosis and limited response to standard treatments. Growing interest in the modulation of DNA repair mechanisms, including the homologous recombination (HR) repair pathway, has opened new avenues for therapeutic development. BARD1 (BRCA1-Associated RING Domain 1) plays a complex role in tumor biology, functioning either as a tumor suppressor or as an oncogenic driver, depending on isoform expression, cellular context, and regulatory environment. In this review, we examine the dual roles of BARD1, focusing on its regulation and paradoxical activities in PDAC. We summarize evidence that BARD1 and BARD1 isoforms differentially affect DNA repair, apoptosis, and drug resistance and evaluate the therapeutic potential of targeting BARD1 and other DNA damage response (DDR) proteins. We also review ongoing clinical trials and investigational agents designed to exploit DDR vulnerabilities in PDAC. Together, these insights highlight BARD1's context-dependent roles in PDAC and support continued efforts to profile BARD1 isoforms, clarify their functions, and leverage DDR pathways through precision oncology approaches.
胰腺导管腺癌(PDAC)是一种侵袭性实体恶性肿瘤,总体预后较差,对标准治疗的反应有限。人们对包括同源重组(HR)修复途径在内的DNA修复机制调节的兴趣日益浓厚,为治疗发展开辟了新途径。BARD1(BRCA1相关环结构域1)在肿瘤生物学中发挥着复杂作用,根据异构体表达、细胞环境和调节环境,它既可以作为肿瘤抑制因子,也可以作为致癌驱动因子。在本综述中,我们研究了BARD1的双重作用,重点关注其在PDAC中的调节和矛盾活性。我们总结了BARD1及其异构体对DNA修复、细胞凋亡和耐药性有不同影响的证据,并评估了靶向BARD1和其他DNA损伤反应(DDR)蛋白的治疗潜力。我们还回顾了旨在利用PDAC中DDR弱点的正在进行的临床试验和研究药物。总之,这些见解突出了BARD1在PDAC中依赖于背景的作用,并支持继续努力分析BARD1异构体、阐明其功能,并通过精准肿瘤学方法利用DDR途径。