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![Radiosynthesis of 1-2-[18F]Fluoroethyl-L-Tryptophan using a One-pot, Two-step Protocol](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F63025.jpg&w=3840&q=50)
Radiosynthesis of 1-2-[18F]Fluoroethyl-L-Tryptophan using a One-pot, Two-step Protocol
Published on: September 21, 2021
Tryptophan metabolism in digestive system tumors: unraveling the pathways and implications
Liang Yu1, Juan Lu2, Weibo Du3
1State Key Laboratory for Diagnosis, Treatment of Infectious Diseases,, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, National Medical Center for Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, No. 79 Qingchun Road, Shangcheng District, Hangzhou, Zhejiang, 310003, China.
Abstract:
Tryptophan (Trp) metabolism plays a crucial role in influencing the development of digestive system tumors. Dysregulation of Trp and its metabolites has been identified in various digestive system cancers, including esophageal, gastric, liver, colorectal, and pancreatic cancers. Aberrantly expressed Trp metabolites are associated with diverse clinical features in digestive system tumors. Moreover, the levels of these metabolites can serve as prognostic indicators and predictors of recurrence risk in patients with digestive system tumors. Trp metabolites exert their influence on tumor growth and metastasis through multiple mechanisms, including immune evasion, angiogenesis promotion, and drug resistance enhancement. Suppressing the expression of key enzymes in Trp metabolism can reduce the accumulation of these metabolites, effectively impacting their role in the promotion of tumor progression and metastasis. Strategies targeting Trp metabolism through specific enzyme inhibitors or tailored drugs exhibit considerable promise in enhancing therapeutic outcomes for digestive system tumors. In addition, integrating these approaches with immunotherapy holds the potential to further enhance treatment efficacy.
Insights
Tryptophan (Trp) metabolism is key in digestive cancers. Targeting Trp metabolites shows promise for improving cancer treatment and predicting patient outcomes.
Area of Science:
- Biochemistry
- Oncology
- Metabolomics
Background:
- Tryptophan (Trp) metabolism is implicated in digestive system tumor development.
- Dysregulated Trp metabolites are found in esophageal, gastric, liver, colorectal, and pancreatic cancers.
- Aberrant Trp metabolites correlate with clinical features and can predict prognosis and recurrence risk.
Purpose of the Study:
- To explore the role of tryptophan metabolism in digestive system tumors.
- To investigate tryptophan metabolites as prognostic and predictive biomarkers.
- To evaluate therapeutic strategies targeting tryptophan metabolism.
Main Methods:
- Analysis of tryptophan metabolite levels in digestive system tumors.
- Correlation of metabolite levels with clinical features and patient outcomes.
- Assessment of the impact of targeting tryptophan metabolism enzymes.
Main Results:
- Tryptophan metabolites are associated with tumor growth, metastasis, immune evasion, angiogenesis, and drug resistance.
- Suppression of key enzymes in Trp metabolism reduces metabolite accumulation and tumor progression.
- Trp metabolite levels serve as prognostic indicators and recurrence predictors.
Conclusions:
- Targeting tryptophan metabolism offers a promising therapeutic strategy for digestive system tumors.
- Enzyme inhibitors and tailored drugs show potential for enhancing treatment outcomes.
- Combination therapy with immunotherapy may improve treatment efficacy.
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