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Gastrointestinal tract microbiota (None. Widely referred to as “gut microbiota,” but no standardized abbreviation as for molecular targets)

Target
None. Widely referred to as “gut microbiota,” but no standardized abbreviation as for molecular targets
Molecular classification
Other
01

Overview

The gastrointestinal tract microbiota refers to the ecosystem of trillions of microorganisms (including bacteria, archaea, viruses, and fungi) inhabiting the human gut from the stomach to the colon. These microbes carry out essential physiological functions for their host, such as metabolizing dietary fiber, synthesizing vitamins, tuning immune responses, maintaining gut barrier integrity, and protecting against pathogens. The composition and activity of the gut microbiota is highly variable between individuals and can profoundly influence the effectiveness and toxicity of drugs, susceptibility to disease, and the outcome of therapies such as cancer immunotherapy. While the gut microbiota can be manipulated by antibiotics, probiotics, prebiotics, or fecal microbiota transplantation, it is not itself a molecular drug target; rather, it represents a complex and dynamic biological system whose balance is fundamental to health and disease.

Other names
Gut microbiotaGut floraIntestinal floraGut microbial communityGut microflora (older usage; now largely deprecated)Gastrointestinal microbiota
02

Mechanism of action

Restoration or modulation of microbial diversity (e.g., FMT) Direct suppression or promotion of specific bacteria (antibiotics, probiotics, prebiotics) Inhibition of specific bacterial enzymes (e.g., β-glucuronidase inhibitors to prevent irinotecan toxicity) Enhancement or suppression of host immune response by altering microbiota composition

03

Biological functions

Metabolism of nutrients and xenobioticsSynthesis of vitamins and bioactive metabolitesFermentation of dietary fibers to short-chain fatty acidsRegulation of immune responsesProtection against pathogensMaintenance of gut barrier integrity
04

Disease associations

Inflammation (inflammatory bowel disease, irritable bowel syndrome)Infection (Clostridium difficile and other pathogens)Cancer (especially colorectal cancer and response to immunotherapy)Cardiovascular disease (via metabolites like TMAO)Metabolic diseases (obesity, type 2 diabetes)Neuropsychiatric conditions (“gut-brain axis”)Other (allergy, autoimmune, liver and chronic diseases)
05

Safety considerations

Risk of transferring antibiotic resistance or pathogens via FMTUnpredictable effects (e.g., dysbiosis) of broad-spectrum antibiotics or probioticsDifficulty in targeting specific bacterial strains without disrupting the overall ecosystemPotential for adverse immune responses or metabolic shifts
06

Interacting drugs

Antibiotics (broadly alter gut microbiota composition)

3 more in the full profile.

07

Biomarkers

Microbial diversity or specific taxa abundance (e.g., increased Firmicutes/Bacteroidetes ratio)Microbial metabolites (e.g., short-chain fatty acids, TMAO, secondary bile acids)Patterns of dysbiosis as indicators for disease risk or drug response

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