Amarsanaa Enkhzul, Oh Jung-Min, Lee Seon Young, Maiti Saikat, Hong Sung You, Myung Kyungjae
Center for Genomic Integrity (CGI), Institute for Basic Science (IBS), Ulsan, Republic of Korea.
Department of Biological Sciences, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea.
Anim Cells Syst (Seoul). 2025 Aug 4;29(1):502-511. doi: 10.1080/19768354.2025.2542172. eCollection 2025.
Mismatch repair (MMR) deficiency is a hallmark of microsatellite instability (MSI) in hereditary non-polyposis colorectal cancer, Lynch syndrome, contributing to resistance against conventional chemotherapy and posing a significant therapeutic challenge. In this study, we introduce UNI110, a novel small molecule derived from Baicalein, engineered for enhanced selectivity against MMR-deficient cancer cells. UNI110 exhibits a remarkable sevenfold increase in potency over Baicalein, demonstrating significantly lower IC50 values and heightened cytotoxic effects in MMR-deficient cell lines. Mechanistically, UNI110 selectively induces DNA damage in MMR-deficient cancer cells, ultimately resulting in cell death. Furthermore, UNI110 disrupts homologous recombination (HR) repair by inhibiting the MSH2-MSH3 complex, specifically blocking the interaction between MSH2 and EXO1, thereby impairing long-range end resection during double-strand break (DSB) repair. These findings establish UNI110 as a promising lead compound for the targeted treatment of MMR-deficient colorectal cancers, offering a potential breakthrough in overcoming chemotherapy resistance and improving patient outcomes.
错配修复(MMR)缺陷是遗传性非息肉病性结直肠癌(林奇综合征)中微卫星不稳定性(MSI)的一个标志,它导致对传统化疗产生耐药性,并带来重大的治疗挑战。在本研究中,我们引入了UNI110,这是一种源自黄芩素的新型小分子,经设计可增强对MMR缺陷癌细胞的选择性。与黄芩素相比,UNI110的效力显著提高了七倍,在MMR缺陷细胞系中表现出明显更低的半数抑制浓度(IC50)值和更强的细胞毒性作用。从机制上讲,UNI110在MMR缺陷癌细胞中选择性地诱导DNA损伤,最终导致细胞死亡。此外,UNI110通过抑制MSH2-MSH3复合物来破坏同源重组(HR)修复,特别是阻断MSH2与EXO1之间的相互作用,从而损害双链断裂(DSB)修复过程中的长距离末端切除。这些发现确立了UNI110作为治疗MMR缺陷型结直肠癌的有前景的先导化合物,为克服化疗耐药性和改善患者预后提供了潜在的突破。