Gunasekaran Pethaiah, Shin Sang Chul, Hwang Yeon Sil, Lee Jihyeon, La Yeo Kyung, Yim Min Su, Kim Hak Nam, Kim Tae Wan, Yang Eunjung, Lee Soo Jae, Yoon Jung Min, Kim Eunice EunKyeong, Jeon Seob, Ryu Eun Kyoung, Bang Jeong Kyu
Division of Magnetic Resonance, Korea Basic Science Institute (KBSI), Ochang, Cheongju 28119, Republic of Korea.
Dandicure Inc., Ochang, Cheongju 28119, Republic of Korea.
Pharmaceutics. 2025 Aug 7;17(8):1027. doi: 10.3390/pharmaceutics17081027.
: Cervical cancer remains a major global health concern, with existing chemotherapy facing limited effectiveness owing to resistance. Polo-like kinase 1 (PLK1) overexpression in cervical cancer cells is a promising target for developing novel therapies to overcome chemoresistance and improve treatment efficacy. : In this study, we developed a novel PROTAC, NC1, targeting PLK1 PBD via the N-end rule pathway. : This PROTAC effectively depleted the PLK1 protein in HeLa cells by inducing protein degradation. The crystal structure of the PBD-NC1 complex identified key PLK1 PBD binding interactions and isothermal titration calorimetry (ITC) confirmed a binding affinity of 6.06 µM between NC1 and PLK1 PBD. NC1 significantly decreased cell viability with an IC of 5.23 µM, induced G2/M phase arrest, and triggered apoptosis in HeLa cells. In vivo, NC1 suppressed tumor growth in a HeLa xenograft mouse model. : This research highlights the potential of N-degron-based PROTACs targeting the PLK1 protein in cancer therapies, highlighting their potential in future cervical anticancer treatment strategies.
宫颈癌仍然是全球主要的健康问题,由于耐药性,现有的化疗效果有限。宫颈癌细胞中 polo 样激酶 1(PLK1)的过表达是开发新型疗法以克服化疗耐药性并提高治疗效果的一个有前景的靶点。在本研究中,我们通过 N 端规则途径开发了一种新型靶向 PLK1 PBD 的 PROTAC(NC1)。这种 PROTAC 通过诱导蛋白质降解有效降低了 HeLa 细胞中的 PLK1 蛋白水平。PBD-NC1 复合物的晶体结构确定了关键的 PLK1 PBD 结合相互作用,等温滴定量热法(ITC)证实 NC1 与 PLK1 PBD 之间的结合亲和力为 6.06 µM。NC1 显著降低细胞活力,IC50 为 5.23 µM,诱导 HeLa 细胞 G2/M 期阻滞并引发凋亡。在体内,NC1 在 HeLa 异种移植小鼠模型中抑制肿瘤生长。这项研究突出了基于 N 端规则的 PROTAC 靶向 PLK1 蛋白在癌症治疗中的潜力,彰显了其在未来宫颈癌抗癌治疗策略中的潜力。