» Articles » PMID: 27863401

Isoliquiritigenin Decreases the Incidence of Colitis-associated Colorectal Cancer by Modulating the Intestinal Microbiota

Overview
Journal Oncotarget
Specialty Oncology
Date 2016 Nov 19
PMID 27863401
Citations 39
Authors
Affiliations
Soon will be listed here.
Abstract

Imbalances in intestinal bacteria correlate with colitis-associated colorectal cancer (CAC). Traditional Chinese medicines have been used to adjust the gut microbiota, and isoliquiritigenin (ISL), a flavonoid extracted from licorice, has shown antitumor efficacy. In this study, the effects of ISL on CAC development and the gut microbiota were evaluated using an azoxymethane and dextran sulphate sodium (AOM/DSS)-induced mouse model of CAC (CACM). Histopathological analysis suggested that ISL reduced tumor incidence in vivo. Moreover, high-throughput sequencing and terminal restriction fragment length polymorphism (T-RFLP) studies of the bacterial 16S rRNA gene revealed that the structure of the gut microbial community shifted significantly following AOM/DSS treatment, and that effect was alleviated by treatment with high-dose ISL (150 mg/kg). Compared to the microbiota in the control mice (CK), the levels of Bacteroidetes decreased and the levels of Firmicutes increased during CAC development. ISL reversed the imbalance at the phylum level and altered the familial constituents of the gut microbiota. Specifically, the abundance of Helicobacteraceae increased after treatment with high-dose ISL, while the abundance of Lachnospiraceae and Rikenellaceae decreased. At the genus level, ISL reduced the abundance of opportunistic pathogens (Escherichia and Enterococcus), and increased the levels of probiotics, particularly butyrate-producing bacteria (Butyricicoccus, Clostridium, and Ruminococcus). Thus, ISL protects mice from AOM/DSS-induced CAC, and ISL and the gut microbiota may have synergistic anti-cancer effects.

Citing Articles

Therapeutic potential of flavonoids in gastrointestinal cancer: Focus on signaling pathways and improvement strategies (Review).

Ding Y, Yu Y Mol Med Rep. 2025; 31(4).

PMID: 40017144 PMC: 11884236. DOI: 10.3892/mmr.2025.13474.


Association analysis of gut microbiota with LDL-C metabolism and microbial pathogenicity in colorectal cancer patients.

Qin M, Huang Z, Huang Y, Huang X, Chen C, Wu Y Lipids Health Dis. 2024; 23(1):367.

PMID: 39516755 PMC: 11546423. DOI: 10.1186/s12944-024-02333-4.


Yoyo Dieting, Post-Obesity Weight Loss, and Their Relationship with Gut Health.

Phuong-Nguyen K, McGee S, Aston-Mourney K, Mcneill B, Mahmood M, Rivera L Nutrients. 2024; 16(18).

PMID: 39339770 PMC: 11435324. DOI: 10.3390/nu16183170.


Circadian Rhythm Perturbation Aggravates Gut Microbiota Dysbiosis in Dextran Sulfate Sodium-Induced Colitis in Mice.

Amara J, Itani T, Hajal J, Bakhos J, Saliba Y, Aboushanab S Nutrients. 2024; 16(2).

PMID: 38257139 PMC: 10819604. DOI: 10.3390/nu16020247.


Chemical Composition of Methanol Extracts from Leaves and Flowers of (Ranunculaceae).

Kostikova V, Petrova N, Chernonosov A, Koval V, Kovaleva E, Wang W Int J Mol Sci. 2024; 25(2).

PMID: 38256067 PMC: 10816090. DOI: 10.3390/ijms25020989.


References
1.
Kaci G, Goudercourt D, Dennin V, Pot B, Dore J, Ehrlich S . Anti-inflammatory properties of Streptococcus salivarius, a commensal bacterium of the oral cavity and digestive tract. Appl Environ Microbiol. 2013; 80(3):928-34. PMC: 3911234. DOI: 10.1128/AEM.03133-13. View

2.
Kelly D, Campbell J, King T, Grant G, Jansson E, Coutts A . Commensal anaerobic gut bacteria attenuate inflammation by regulating nuclear-cytoplasmic shuttling of PPAR-gamma and RelA. Nat Immunol. 2003; 5(1):104-12. DOI: 10.1038/ni1018. View

3.
Balamurugan R, Rajendiran E, George S, Vijay Samuel G, Ramakrishna B . Real-time polymerase chain reaction quantification of specific butyrate-producing bacteria, Desulfovibrio and Enterococcus faecalis in the feces of patients with colorectal cancer. J Gastroenterol Hepatol. 2008; 23(8 Pt 1):1298-303. DOI: 10.1111/j.1440-1746.2008.05490.x. View

4.
Gaur R, Gupta V, Singh P, Pal A, Darokar M, Bhakuni R . Drug Resistance Reversal Potential of Isoliquiritigenin and Liquiritigenin Isolated from Glycyrrhiza glabra Against Methicillin-Resistant Staphylococcus aureus (MRSA). Phytother Res. 2016; 30(10):1708-1715. DOI: 10.1002/ptr.5677. View

5.
Liang X, Li H, Tian G, Li S . Dynamic microbe and molecule networks in a mouse model of colitis-associated colorectal cancer. Sci Rep. 2014; 4:4985. PMC: 4021569. DOI: 10.1038/srep04985. View