Gegen Qinlian Decoction Attenuates Colitis-Associated Colorectal Cancer via Suppressing TLR4 Signaling Pathway Based on Network Pharmacology and In Vivo/In Vitro Experimental Validation

<b>Background</b>: Gegen Qinlian Decoction (GQD), is used for intestinal disorders like ulcerative colitis, irritable bowel syndrome, and colorectal cancer. But the precise mechanisms underlying its anti-inflammatory and anti-tumor effects are not fully elucidated. <b>Methods</b...

Full description

Saved in:
Bibliographic Details
Main Authors: Yaoyao Xu, Qiaoyan Cai, Chunyu Zhao, Weixiang Zhang, Xinting Xu, Haowei Lin, Yuxing Lin, Daxin Chen, Shan Lin, Peizhi Jia, Meiling Wang, Ling Zhang, Wei Lin
Format: Article
Language:English
Published: MDPI AG 2024-12-01
Series:Pharmaceuticals
Subjects:
Online Access:https://www.mdpi.com/1424-8247/18/1/12
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832587750056919040
author Yaoyao Xu
Qiaoyan Cai
Chunyu Zhao
Weixiang Zhang
Xinting Xu
Haowei Lin
Yuxing Lin
Daxin Chen
Shan Lin
Peizhi Jia
Meiling Wang
Ling Zhang
Wei Lin
author_facet Yaoyao Xu
Qiaoyan Cai
Chunyu Zhao
Weixiang Zhang
Xinting Xu
Haowei Lin
Yuxing Lin
Daxin Chen
Shan Lin
Peizhi Jia
Meiling Wang
Ling Zhang
Wei Lin
author_sort Yaoyao Xu
collection DOAJ
description <b>Background</b>: Gegen Qinlian Decoction (GQD), is used for intestinal disorders like ulcerative colitis, irritable bowel syndrome, and colorectal cancer. But the precise mechanisms underlying its anti-inflammatory and anti-tumor effects are not fully elucidated. <b>Methods</b>: Use network pharmacology to identify targets and pathways of GQD. In vivo (azoxymethane/dextran sodium sulfate (AOM/DSS)-induced colitis-associated colorectal cancer (CAC) mouse model) and in vitro (lipopolysaccharide (LPS)-stimulated RAW264.7 macrophages) experiments were conducted to explore GQD’s anti-inflammatory and anti-tumor effects. We monitored mouse body weight and disease activity index (DAI), and evaluated colon cancer tissues using hematoxylin and eosin staining. Expression of Ki67 and F4/80 was determined by immunohistochemistry analysis. The protein levels of TLR4 signaling pathway were assessed by western blotting analysis. Enzyme-linked immunosorbent assay measured IL-1β, IL-6, and TNF-α levels. Immunofluorescence (IF) staining visualized NF-κB and IRF3 translocation. <b>Results</b>: There were 18, 9, 24 and 77 active ingredients in the four herbs of GQD, respectively, targeting 435, 156, 485 and 691 genes. Through data platform analysis, it was concluded that there were 1104 target genes of GQD and 2022 target genes of CAC. Moreover, there were 99 intersecting genes between GQD and CAC. The core targets of GQD contained NFKB1, IL1B, IL6, TLR4, and TNF, and GQD reduced inflammation by inhibiting the TLR4 signaling pathway. In vivo experiment, GQD increased mouse body weight, lowered DAI scores, while also alleviating histopathological changes in the colon and decreasing the expressions of Ki67 and F4/80 in the AOM/DSS-induced mice. GQD reduced IL-1β, IL-6, and TNF-α levels in the serum and downregulated TLR4, MyD88, and phosphorylation of IκBα, P65, and IRF3 in the colon tissue from AOM/DSS-induced mice. In vitro, GQD suppressed pro-inflammatory cytokines and TLR4 signaling pathway in the LPS-induced RAW264.7 cells, and combined with TAK242, it further reduced the phosphorylation of IκBα, P65. <b>Conclusions</b>: GQD mitigated CAC by inhibiting the TLR4 signaling pathway, offering a potential therapeutic approach for CAC management.
format Article
id doaj-art-e9376332d5674c74b84ed68d04b84da3
institution Kabale University
issn 1424-8247
language English
publishDate 2024-12-01
publisher MDPI AG
record_format Article
series Pharmaceuticals
spelling doaj-art-e9376332d5674c74b84ed68d04b84da32025-01-24T13:45:00ZengMDPI AGPharmaceuticals1424-82472024-12-011811210.3390/ph18010012Gegen Qinlian Decoction Attenuates Colitis-Associated Colorectal Cancer via Suppressing TLR4 Signaling Pathway Based on Network Pharmacology and In Vivo/In Vitro Experimental ValidationYaoyao Xu0Qiaoyan Cai1Chunyu Zhao2Weixiang Zhang3Xinting Xu4Haowei Lin5Yuxing Lin6Daxin Chen7Shan Lin8Peizhi Jia9Meiling Wang10Ling Zhang11Wei Lin12Academy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaAcademy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaAcademy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaAcademy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaAcademy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaAcademy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaAcademy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaInnovation and Transformation Center, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaAcademy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaAcademy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaAcademy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaAcademy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaInnovation and Transformation Center, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, China<b>Background</b>: Gegen Qinlian Decoction (GQD), is used for intestinal disorders like ulcerative colitis, irritable bowel syndrome, and colorectal cancer. But the precise mechanisms underlying its anti-inflammatory and anti-tumor effects are not fully elucidated. <b>Methods</b>: Use network pharmacology to identify targets and pathways of GQD. In vivo (azoxymethane/dextran sodium sulfate (AOM/DSS)-induced colitis-associated colorectal cancer (CAC) mouse model) and in vitro (lipopolysaccharide (LPS)-stimulated RAW264.7 macrophages) experiments were conducted to explore GQD’s anti-inflammatory and anti-tumor effects. We monitored mouse body weight and disease activity index (DAI), and evaluated colon cancer tissues using hematoxylin and eosin staining. Expression of Ki67 and F4/80 was determined by immunohistochemistry analysis. The protein levels of TLR4 signaling pathway were assessed by western blotting analysis. Enzyme-linked immunosorbent assay measured IL-1β, IL-6, and TNF-α levels. Immunofluorescence (IF) staining visualized NF-κB and IRF3 translocation. <b>Results</b>: There were 18, 9, 24 and 77 active ingredients in the four herbs of GQD, respectively, targeting 435, 156, 485 and 691 genes. Through data platform analysis, it was concluded that there were 1104 target genes of GQD and 2022 target genes of CAC. Moreover, there were 99 intersecting genes between GQD and CAC. The core targets of GQD contained NFKB1, IL1B, IL6, TLR4, and TNF, and GQD reduced inflammation by inhibiting the TLR4 signaling pathway. In vivo experiment, GQD increased mouse body weight, lowered DAI scores, while also alleviating histopathological changes in the colon and decreasing the expressions of Ki67 and F4/80 in the AOM/DSS-induced mice. GQD reduced IL-1β, IL-6, and TNF-α levels in the serum and downregulated TLR4, MyD88, and phosphorylation of IκBα, P65, and IRF3 in the colon tissue from AOM/DSS-induced mice. In vitro, GQD suppressed pro-inflammatory cytokines and TLR4 signaling pathway in the LPS-induced RAW264.7 cells, and combined with TAK242, it further reduced the phosphorylation of IκBα, P65. <b>Conclusions</b>: GQD mitigated CAC by inhibiting the TLR4 signaling pathway, offering a potential therapeutic approach for CAC management.https://www.mdpi.com/1424-8247/18/1/12Gegen Qinlian Decoctioncolitis-associated colorectal cancerazoxymethane/dextran sodium sulfateinflammatory responsenetwork pharmacologyTLR4 signaling pathway
spellingShingle Yaoyao Xu
Qiaoyan Cai
Chunyu Zhao
Weixiang Zhang
Xinting Xu
Haowei Lin
Yuxing Lin
Daxin Chen
Shan Lin
Peizhi Jia
Meiling Wang
Ling Zhang
Wei Lin
Gegen Qinlian Decoction Attenuates Colitis-Associated Colorectal Cancer via Suppressing TLR4 Signaling Pathway Based on Network Pharmacology and In Vivo/In Vitro Experimental Validation
Pharmaceuticals
Gegen Qinlian Decoction
colitis-associated colorectal cancer
azoxymethane/dextran sodium sulfate
inflammatory response
network pharmacology
TLR4 signaling pathway
title Gegen Qinlian Decoction Attenuates Colitis-Associated Colorectal Cancer via Suppressing TLR4 Signaling Pathway Based on Network Pharmacology and In Vivo/In Vitro Experimental Validation
title_full Gegen Qinlian Decoction Attenuates Colitis-Associated Colorectal Cancer via Suppressing TLR4 Signaling Pathway Based on Network Pharmacology and In Vivo/In Vitro Experimental Validation
title_fullStr Gegen Qinlian Decoction Attenuates Colitis-Associated Colorectal Cancer via Suppressing TLR4 Signaling Pathway Based on Network Pharmacology and In Vivo/In Vitro Experimental Validation
title_full_unstemmed Gegen Qinlian Decoction Attenuates Colitis-Associated Colorectal Cancer via Suppressing TLR4 Signaling Pathway Based on Network Pharmacology and In Vivo/In Vitro Experimental Validation
title_short Gegen Qinlian Decoction Attenuates Colitis-Associated Colorectal Cancer via Suppressing TLR4 Signaling Pathway Based on Network Pharmacology and In Vivo/In Vitro Experimental Validation
title_sort gegen qinlian decoction attenuates colitis associated colorectal cancer via suppressing tlr4 signaling pathway based on network pharmacology and in vivo in vitro experimental validation
topic Gegen Qinlian Decoction
colitis-associated colorectal cancer
azoxymethane/dextran sodium sulfate
inflammatory response
network pharmacology
TLR4 signaling pathway
url https://www.mdpi.com/1424-8247/18/1/12
work_keys_str_mv AT yaoyaoxu gegenqinliandecoctionattenuatescolitisassociatedcolorectalcancerviasuppressingtlr4signalingpathwaybasedonnetworkpharmacologyandinvivoinvitroexperimentalvalidation
AT qiaoyancai gegenqinliandecoctionattenuatescolitisassociatedcolorectalcancerviasuppressingtlr4signalingpathwaybasedonnetworkpharmacologyandinvivoinvitroexperimentalvalidation
AT chunyuzhao gegenqinliandecoctionattenuatescolitisassociatedcolorectalcancerviasuppressingtlr4signalingpathwaybasedonnetworkpharmacologyandinvivoinvitroexperimentalvalidation
AT weixiangzhang gegenqinliandecoctionattenuatescolitisassociatedcolorectalcancerviasuppressingtlr4signalingpathwaybasedonnetworkpharmacologyandinvivoinvitroexperimentalvalidation
AT xintingxu gegenqinliandecoctionattenuatescolitisassociatedcolorectalcancerviasuppressingtlr4signalingpathwaybasedonnetworkpharmacologyandinvivoinvitroexperimentalvalidation
AT haoweilin gegenqinliandecoctionattenuatescolitisassociatedcolorectalcancerviasuppressingtlr4signalingpathwaybasedonnetworkpharmacologyandinvivoinvitroexperimentalvalidation
AT yuxinglin gegenqinliandecoctionattenuatescolitisassociatedcolorectalcancerviasuppressingtlr4signalingpathwaybasedonnetworkpharmacologyandinvivoinvitroexperimentalvalidation
AT daxinchen gegenqinliandecoctionattenuatescolitisassociatedcolorectalcancerviasuppressingtlr4signalingpathwaybasedonnetworkpharmacologyandinvivoinvitroexperimentalvalidation
AT shanlin gegenqinliandecoctionattenuatescolitisassociatedcolorectalcancerviasuppressingtlr4signalingpathwaybasedonnetworkpharmacologyandinvivoinvitroexperimentalvalidation
AT peizhijia gegenqinliandecoctionattenuatescolitisassociatedcolorectalcancerviasuppressingtlr4signalingpathwaybasedonnetworkpharmacologyandinvivoinvitroexperimentalvalidation
AT meilingwang gegenqinliandecoctionattenuatescolitisassociatedcolorectalcancerviasuppressingtlr4signalingpathwaybasedonnetworkpharmacologyandinvivoinvitroexperimentalvalidation
AT lingzhang gegenqinliandecoctionattenuatescolitisassociatedcolorectalcancerviasuppressingtlr4signalingpathwaybasedonnetworkpharmacologyandinvivoinvitroexperimentalvalidation
AT weilin gegenqinliandecoctionattenuatescolitisassociatedcolorectalcancerviasuppressingtlr4signalingpathwaybasedonnetworkpharmacologyandinvivoinvitroexperimentalvalidation