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Table 2 Research on the application of trp metabolism in digestive system tumors

From: Tryptophan metabolism in digestive system tumors: unraveling the pathways and implications

Targeted agents

Diseases

Molecules targeted

Outcomes

Ref

1-MT

Colorectal cancer

IDO

Inhibit cell proliferation, and tumor growth

[67]

1-MT

Pancreatic cancer

IDO

Motivate antitumor responses, and elicit tumor inflammatory necrosis

[90]

1-L-MT

Colorectal cancer

IDO

Inhibit cell proliferation, and tumor growth

[89]

Sertaconazole nitrate

Colorectal cancer

IDO1

Induce autophagy and apoptosis, and inhibit tumor growth

[92]

INCB023843, and INCB024360

Pancreatic cancer, and colorectal cancer

IDO

Inhibit the growth of IDO-expressing tumors

[93]

Hydrogen sulfide

Hepatocellular carcinoma

IDO1

Decrease microvasculature density, and enhance tumor cell apoptosis

[94]

Carbidopa

Pancreatic cancer

AHR, IDO1

Inhibit tumor growth

[96]

USP14

Colorectal cancer

IDO1

Promote immune suppression

[98]

Sodium tanshinone IIA sulfonate

Colorectal cancer

IDO1/TDO2

Enhance Anti-PD1 Therapy

[99]

RY103

Pancreatic cancer

IDO1/TDO

Inhibit cell migration, invasion, and tumor growth

[100]

GR127935

Colorectal cancer

5-HT1DR

Inhibit cell invasion, and tumor metastasis

[101]

Sb204741

Pancreatic cancer

HTR2B

Inhibit tumor growth

[77]

PF06845102/EOS200809

Colorectal cancer

TDO

Improve the efficacy of checkpoint inhibitors

[102]

Combination of Navoximod, and Atezolizumab

Pancreatic cancer

IDO1

Not offer convincing evidence of enhancement compared to single-agent therapy

[97]

Combination of Abrine, and Anti-PD-1 antibody

Hepatocellular carcinoma

IDO1

Reduce immune escape

[95]

Combination of 1-MT, and Radiation

Colorectal cancer

IDO

Enhance radiosensitivity

[103]

Combination of Rosmarinic acid, and IDO1-shRNA

Hepatocellular carcinoma

IDO

Inhibit tumor growth

[104]