King Faisal Specialist Hospital and Research Center- Research Center, KFSH&RC, MBC-J04, P.O. Box 40047, Jeddah, 21499, Saudi Arabia.
College of Medicine, Al-Faisal University, P.O. Box 50927, Riyadh, 11533, Saudi Arabia.
BMC Cancer. 2022 Jun 1;22(1):599. doi: 10.1186/s12885-022-09567-4.
The full-length BRCA1-associated RING domain 1 (BARD1) gene encodes a 777-aa protein. BARD1 displays a dual role in cancer development and progression as it acts as a tumor suppressor and an oncogene. Structurally, BARD1 has homologous domains to BRCA1 that aid their heterodimer interaction to inhibit the progression of different cancers such as breast and ovarian cancers following the BRCA1-dependant pathway. In addition, BARD1 was shown to be involved in other pathways that are involved in tumor suppression (BRCA1-independent pathway) such as the TP53-dependent apoptotic signaling pathway. However, there are abundant BARD1 isoforms exist that are different from the full-length BARD1 due to nonsense and frameshift mutations, or deletions were found to be associated with susceptibility to various cancers including neuroblastoma, lung, breast, and cervical cancers. This article reviews the spectrum of BARD1 full-length genes and its different isoforms and their anticipated associated risk. Additionally, the study also highlights the role of BARD1 as an oncogene in breast cancer patients and its potential uses as a prognostic/diagnostic biomarker and as a therapeutic target for cancer susceptibility testing and treatment.
全长 BRCA1 相关环结构域 1(BARD1)基因编码一个 777 个氨基酸的蛋白质。BARD1 在癌症的发生和发展中具有双重作用,既是肿瘤抑制因子,也是癌基因。结构上,BARD1 与 BRCA1 具有同源结构域,有助于它们的异二聚体相互作用,抑制不同癌症的进展,如乳腺癌和卵巢癌,这是通过 BRCA1 依赖途径实现的。此外,BARD1 还被证明参与其他涉及肿瘤抑制的途径(BRCA1 非依赖性途径),如 TP53 依赖性凋亡信号通路。然而,由于无义和移码突变,或者发现缺失与各种癌症的易感性有关,包括神经母细胞瘤、肺癌、乳腺癌和宫颈癌,存在大量与全长 BARD1 不同的 BARD1 异构体。本文综述了 BARD1 全长基因及其不同异构体的范围及其预期的相关风险。此外,该研究还强调了 BARD1 作为乳腺癌患者癌基因的作用及其作为预后/诊断生物标志物的潜在用途,以及作为癌症易感性测试和治疗的治疗靶点。