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硫酸吲哚酚在慢性肾脏病进展过程中加重结直肠癌的作用:对HCT-116结肠癌细胞中Akt/β-连环蛋白/c-Myc和芳烃受体/c-Myc信号通路的见解

The Role of Indoxyl Sulfate in Exacerbating Colorectal Cancer During Chronic Kidney Disease Progression: Insights into the Akt/β-Catenin/c-Myc and AhR/c-Myc Pathways in HCT-116 Colorectal Cancer Cells.

作者信息

Ichisaka Yu, Takei Chihiro, Naito Kazuma, Higa Manami, Yano Shozo, Niwa Toshimitsu, Shimizu Hidehisa

机构信息

Graduate School of Natural Science and Technology, Shimane University, 1060 Nishikawatsu-cho, Matsue 690-8504, Shimane, Japan.

Faculty of Medicine, Shimane University, 89-1 Enya-cho, Izumo 693-8501, Shimane, Japan.

出版信息

Toxins (Basel). 2025 Jan 1;17(1):17. doi: 10.3390/toxins17010017.

Abstract

Epidemiological studies suggest an increased risk of colorectal cancer (CRC) aggravation in patients with chronic kidney disease (CKD). Our previous study demonstrated that indoxyl sulfate, a uremic toxin whose concentration increases with CKD progression, exacerbates CRC through activation of the AhR and Akt pathways. Consequently, indoxyl sulfate has been proposed to be a significant link between CKD progression and CRC aggravation. The present study aimed to investigate the roles of c-Myc and β-Catenin, which are hypothesized to be downstream factors of indoxyl sulfate-induced AhR and Akt activation, in CRC cell proliferation and EGF sensitivity in HCT-116 CRC cells. Indoxyl sulfate significantly induced CRC cell proliferation at concentrations exceeding 62.5 µM, a process suppressed by the c-Myc inhibitor 10058-F4. Indoxyl sulfate activated the Akt/β-Catenin/c-Myc pathway as evidenced by the Akt inhibitor MK2206, which decreased both β-Catenin and c-Myc protein levels, and the β-Catenin inhibitor XAV-939, which reduced c-Myc protein levels. The AhR antagonist CH223191 also inhibited c-Myc upregulation, indicating involvement of the AhR/c-Myc pathway. MK2206 partially attenuated the indoxyl sulfate-induced AhR transcriptional activity, suggesting that Akt activation influences the AhR/c-Myc pathway. MK2206, CH223191, and 10058-F4 suppressed the increase in EGFR protein levels induced by indoxyl sulfate, indicating that the Akt/β-Catenin/c-Myc and AhR/c-Myc pathways enhance the sensitivity of HCT-116 CRC cells to EGF. These findings indicate that the elevation of indoxyl sulfate levels in the blood, due to CKD progression, could worsen CRC by promoting the proliferation of CRC cells and enhancing EGF signaling. Therefore, indoxyl sulfate could potentially serve as a therapeutic target for CRC aggravation in patients with CKD.

摘要

流行病学研究表明,慢性肾脏病(CKD)患者患结直肠癌(CRC)病情加重的风险增加。我们之前的研究表明,硫酸吲哚酚是一种随着CKD进展而浓度升高的尿毒症毒素,它通过激活芳烃受体(AhR)和Akt信号通路加剧CRC。因此,硫酸吲哚酚被认为是CKD进展与CRC病情加重之间的重要联系。本研究旨在探讨c-Myc和β-连环蛋白的作用,据推测它们是硫酸吲哚酚诱导的AhR和Akt激活的下游因子,在HCT-116 CRC细胞的CRC细胞增殖和表皮生长因子(EGF)敏感性方面的作用。当硫酸吲哚酚浓度超过62.5 µM时,它能显著诱导CRC细胞增殖,这一过程被c-Myc抑制剂10058-F4所抑制。硫酸吲哚酚激活了Akt/β-连环蛋白/c-Myc信号通路,这可通过Akt抑制剂MK2206(它降低了β-连环蛋白和c-Myc蛋白水平)以及β-连环蛋白抑制剂XAV-939(它降低了c-Myc蛋白水平)得以证明。AhR拮抗剂CH223191也抑制了c-Myc的上调,表明AhR/c-Myc信号通路参与其中。MK2206部分减弱了硫酸吲哚酚诱导的AhR转录活性,这表明Akt激活影响AhR/c-Myc信号通路。MK2206、CH223191和10058-F4抑制了硫酸吲哚酚诱导的表皮生长因子受体(EGFR)蛋白水平的升高,表明Akt/β-连环蛋白/c-Myc和AhR/c-Myc信号通路增强了HCT-116 CRC细胞对EGF的敏感性。这些发现表明,由于CKD进展导致血液中硫酸吲哚酚水平升高,可能通过促进CRC细胞增殖和增强EGF信号传导而使CRC病情恶化。因此,硫酸吲哚酚有可能成为CKD患者CRC病情加重的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74c9/11769072/cfbe31cb0072/toxins-17-00017-g001.jpg

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