Discovery of IDO1 Inhibitors: From Bench to Bedside

George C Prendergast1, William P Malachowski2, James B DuHadaway3

  • 1Lankenau Institute for Medical Research (LIMR), Wynnewood, Pennsylvania. prendergast@limr.org.

Cancer Research
|December 17, 2017
PubMed

Insights

Small-molecule inhibitors targeting indoleamine 2,3-dioxygenase-1 (IDO1) show promise in oncology. These IDO1 inhibitors, including indoximod, epacadostat, and navoximod, are being explored to enhance cancer immunotherapies.

Area of Science:

  • Oncology
  • Immunology
  • Pharmacology

Background:

  • Indoleamine 2,3-dioxygenase-1 (IDO1) is an enzyme implicated in cancer immune evasion.
  • Targeting IDO1 is a novel strategy in cancer treatment.
  • Small-molecule IDO1 inhibitors represent a new class of experimental cancer agents.

Related Concept Videos

Drug Discovery: Overview01:26

Drug Discovery: Overview

Drug discovery is a multifaceted process involving extensive screening, testing, and optimization of lead compounds to identify potential new drugs for therapeutic use. It combines several approaches, including screening large numbers of natural products, chemical modification of known active molecules, identification of new drug targets, and rational design based on biological mechanisms and drug-receptor structure. These approaches are carried out in both academic research laboratories and...
12.0K
Inhibition of Cdk Activity02:34

Inhibition of Cdk Activity

The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
6.0K
Pharmacogenomics: Identification of New Drug Targets01:29

Pharmacogenomics: Identification of New Drug Targets

Advances in genomics have profoundly influenced drug discovery by increasing both the speed and accuracy of pharmaceutical development. Pharmacogenomics, which examines how genetic variation influences drug response, facilitates the identification of novel therapeutic targets and enables patient stratification for personalized treatment. These strategies contribute to improved drug efficacy, minimized adverse effects, and more efficient clinical trial design.Mapping genetic differences...
9
Dipeptidyl Peptidase 4 Inhibitors01:23

Dipeptidyl Peptidase 4 Inhibitors

Dipeptidyl peptidase 4 (DPP-4) is a serine protease widely distributed in the body. It's involved in the inactivation of GLP-1 and GIP hormones, which are crucial for insulin regulation. DPP-4 inhibitors, such as sitagliptin (Januvia), saxagliptin (Onglyza), linagliptin (Tradjenta), alogliptin (Nesina), and vildagliptin (Galvus), help increase the proportion of active GLP-1, enhancing insulin secretion. These inhibitors work by competitively binding to DPP-4. This binding causes a...
729