TY - JOUR
T1 - Host-Gut Microbiota Metabolic Interactions and Their Role in Precision Diagnosis and Treatment of Gastrointestinal Cancers
AU - Cao, Chunhao
AU - Yue, Siran
AU - Lu, Aiping
AU - Liang, Chao
N1 - This work is supported by the National Natural Science Foundation Council of China (82172386 and 81922081 to C.L.), the Department of Education of Guangdong Province (2021KTSCX104 to C.L.), the 2020 Guangdong Provincial Science and Technology Innovation Strategy Special Fund (Guangdong-Hong Kong-Macau Joint Lab) (2020B1212030006 to A.L.), the Guangdong Basic and Applied Basic Research Foundation (2022A1515012164 to C.L.), the Science, Technology and Innovation Commission of Shenzhen (JCYJ20210324104201005 to C.L.), the Hong Kong General Research Fund (12102722 to A.L.), and the Hong Kong RGC Theme-based Research Scheme (T12-201/20-R to A.L.)
Publisher Copyright:
© 2024 The Authors
PY - 2024/9
Y1 - 2024/9
N2 - The critical role of the gut microbiome in gastrointestinal cancers is becoming increasingly clear. Imbalances in the gut microbial community, referred to as dysbiosis, are linked to increased risks for various forms of gastrointestinal cancers. Pathogens like Fusobacterium and Helicobacter pylori relate to the onset of esophageal and gastric cancers, respectively, while microbes such as Porphyromonas gingivalis and Clostridium species have been associated with a higher risk of pancreatic cancer. In colorectal cancer, bacteria such as Fusobacterium nucleatum are known to stimulate the growth of tumor cells and trigger cancer-promoting pathways. On the other hand, beneficial microbes like Bifidobacteria offer a protective effect, potentially inhibiting the development of gastrointestinal cancers. The potential for therapeutic interventions that manipulate the gut microbiome is substantial, including strategies to engineer anti-tumor metabolites and employ microbiota-based treatments. Despite the progress in understanding the influence of the microbiome on gastrointestinal cancers, significant challenges remain in identifying and understanding the precise contributions of specific microbial species and their metabolic products. This knowledge is essential for leveraging the role of the gut microbiome in the development of precise diagnostics and targeted therapies for gastrointestinal cancers.
AB - The critical role of the gut microbiome in gastrointestinal cancers is becoming increasingly clear. Imbalances in the gut microbial community, referred to as dysbiosis, are linked to increased risks for various forms of gastrointestinal cancers. Pathogens like Fusobacterium and Helicobacter pylori relate to the onset of esophageal and gastric cancers, respectively, while microbes such as Porphyromonas gingivalis and Clostridium species have been associated with a higher risk of pancreatic cancer. In colorectal cancer, bacteria such as Fusobacterium nucleatum are known to stimulate the growth of tumor cells and trigger cancer-promoting pathways. On the other hand, beneficial microbes like Bifidobacteria offer a protective effect, potentially inhibiting the development of gastrointestinal cancers. The potential for therapeutic interventions that manipulate the gut microbiome is substantial, including strategies to engineer anti-tumor metabolites and employ microbiota-based treatments. Despite the progress in understanding the influence of the microbiome on gastrointestinal cancers, significant challenges remain in identifying and understanding the precise contributions of specific microbial species and their metabolic products. This knowledge is essential for leveraging the role of the gut microbiome in the development of precise diagnostics and targeted therapies for gastrointestinal cancers.
KW - biomarkers
KW - gastrointestinal cancers
KW - gut microbiota
KW - metabolic interactions
KW - microbiome therapeutics
UR - http://www.scopus.com/inward/record.url?scp=85199182778&partnerID=8YFLogxK
U2 - 10.1016/j.phrs.2024.107321
DO - 10.1016/j.phrs.2024.107321
M3 - Journal article
AN - SCOPUS:85199182778
SN - 1043-6618
VL - 207
JO - Pharmacological Research
JF - Pharmacological Research
M1 - 107321
ER -