Liang Xinghua, Liu Xuelian, Zhang Long, Liu Junhao, Yan Rong, Li Haiyan, Zeng Xiancheng, Wang Hong
The First Clinical Medical College, Jinan University, Guangzhou, China.
Department of Gastroenterology, The Fourth Affiliated Hospital of Guangzhou Medical University (Zengcheng District People`s Hospital of Guangzhou), Guangzhou, China.
Cytojournal. 2024 Nov 16;21:44. doi: 10.25259/Cytojournal_44_2024. eCollection 2024.
Colorectal cancer is severely challenging because of the insufficient understanding of the mechanism underlying its resistance to clinical chemotherapy. The purpose of our study is to investigate the role of the LIM protein Ajuba (JUB) in the chemoresistance of colon cancer and its potential effect on clinical treatment.
The protein levels of JUB in colon cancer tissues were evaluated using Western blot analysis and immunohistochemistry assays. The correlation between JUB and the prognosis of patients with colorectal cancer was determined using Kaplan-Meier plot analysis. 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assays were employed to determine the 50% inhibitory concentration of 5-fluorouracil (5-FU) and thus assess the effect of JUB on the effectiveness of 5-FU. In addition, the rate of cellular apoptosis was measured using fluorescence-activated cell sorting assays. Side population and sphere formation analyses were conducted to determine the role of JUB in promoting the stem cell-like traits of colon cancer cells. assays were performed and detect whether the downregulation of JUB induces 5-FU sensitivity. Moreover, luciferase and Western blot assays were employed to uncover the mechanism through which JUB promotes chemoresistance in colon cancer.
JUB expression was upregulated in chemoresistant colon cancer ( < 0.001) and correlated with relapse-free survival ( = 0.000002). Functionally, the upregulation of JUB conferred 5-FU resistance to colon cancer cells , whereas the downregulation of JUB induced 5-FU sensitivity in colon cancer cells . The high expression of JUB promoted the tumorigenic capability of colon cancer cells. Furthermore, the increased expression of JUB activated multiple downstream genes of the Notch signaling pathway with increased expression in JUB-overexpressing cells but reduced expression in JUB-silenced cells. Importantly, the inhibition of Notch signaling using a small-molecule inhibitor significantly suppressed JUB-induced chemoresistance.
Results suggest that JUB plays an important role and may serve as a biomarker for the clinical treatment of patients with 5-FU-resistant colon cancer.
由于对结直肠癌临床化疗耐药机制的认识不足,其治疗面临严峻挑战。本研究旨在探讨LIM蛋白Ajuba(JUB)在结肠癌化疗耐药中的作用及其对临床治疗的潜在影响。
采用蛋白质免疫印迹分析和免疫组织化学检测评估结肠癌组织中JUB的蛋白水平。使用Kaplan-Meier曲线分析确定JUB与结直肠癌患者预后的相关性。采用3-(4,5-二甲基噻唑-2)-2,5-二苯基四氮唑溴盐法测定5-氟尿嘧啶(5-FU)的50%抑制浓度,从而评估JUB对5-FU疗效的影响。此外,使用荧光激活细胞分选法检测细胞凋亡率。进行侧群细胞和球体形成分析,以确定JUB在促进结肠癌细胞干细胞样特性中的作用。进行实验以检测JUB的下调是否诱导5-FU敏感性。此外,采用荧光素酶和蛋白质免疫印迹分析揭示JUB促进结肠癌化疗耐药的机制。
JUB在化疗耐药的结肠癌中表达上调(<0.001),并与无复发生存期相关(=0.000002)。在功能上,JUB的上调赋予结肠癌细胞5-FU耐药性,而JUB的下调则诱导结肠癌细胞对5-FU敏感。JUB的高表达促进了结肠癌细胞的致瘤能力。此外,JUB表达的增加激活了Notch信号通路的多个下游基因,在JUB过表达细胞中表达增加,而在JUB沉默细胞中表达降低。重要的是,使用小分子抑制剂抑制Notch信号通路可显著抑制JUB诱导的化疗耐药性。
结果表明,JUB发挥重要作用,可能作为5-FU耐药结肠癌患者临床治疗的生物标志物。