Literature DB >> 28324751

The rationale of indoleamine 2,3-dioxygenase inhibition for cancer therapy.

Lieve Brochez1, Ines Chevolet2, Vibeke Kruse3.   

Abstract

Indoleamine 2,3-dioxygenase (IDO, also referred to as IDO1) has been demonstrated to be a normal endogenous mechanism of acquired peripheral immune tolerance in vivo. In the field of oncology, IDO expression and/or activity has been observed in several cancer types and has usually been associated with negative prognostic factors and worse outcome measures. This manuscript reviews current available data on the role of IDO in cancer and the current results obtained with IDO inhibition, both in animal models and in phase 1 and 2 clinical trials in humans. Preliminary results with IDO inhibitors, usually combined with other anti-cancer drugs, seem encouraging. Further studies are needed to clarify the conditions in which IDO inhibitors can be of value as an anti-cancer strategy. In addition, further research should address whether the expression of IDO in tissue or blood can be a marker to select patients who can benefit most from IDO inhibition.
Copyright © 2017. Published by Elsevier Ltd.

Entities:  

Keywords:  Cancer; Epacadostat; IDO inhibition; Immune tolerance; Indoleamine 2-3-dioxygenase (IDO); Indoximod; Melanoma

Mesh:

Substances:

Year:  2017        PMID: 28324751     DOI: 10.1016/j.ejca.2017.01.011

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  107 in total

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Review 3.  Trial Watch: Toll-like receptor agonists in cancer immunotherapy.

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4.  Quantitative Spatial Profiling of PD-1/PD-L1 Interaction and HLA-DR/IDO-1 Predicts Improved Outcomes of Anti-PD-1 Therapies in Metastatic Melanoma.

Authors:  Douglas B Johnson; Jennifer Bordeaux; Ju Young Kim; Christine Vaupel; David L Rimm; Thai H Ho; Richard W Joseph; Adil I Daud; Robert M Conry; Elizabeth M Gaughan; Leonel F Hernandez-Aya; Anastasios Dimou; Pauline Funchain; James Smithy; John S Witte; Svetlana B McKee; Jennifer Ko; John M Wrangle; Bashar Dabbas; Shabnam Tangri; Jelveh Lameh; Jeffrey Hall; Joseph Markowitz; Justin M Balko; Naveen Dakappagari
Journal:  Clin Cancer Res       Date:  2018-07-18       Impact factor: 12.531

Review 5.  Targeting Metalloenzymes for Therapeutic Intervention.

Authors:  Allie Y Chen; Rebecca N Adamek; Benjamin L Dick; Cy V Credille; Christine N Morrison; Seth M Cohen
Journal:  Chem Rev       Date:  2018-09-07       Impact factor: 60.622

6.  Tryptophan catabolism reflects disease activity in human tuberculosis.

Authors:  Jeffrey M Collins; Amnah Siddiqa; Dean P Jones; Ken Liu; Russell R Kempker; Azhar Nizam; N Sarita Shah; Nazir Ismail; Samuel G Ouma; Nestani Tukvadze; Shuzhao Li; Cheryl L Day; Jyothi Rengarajan; James Cm Brust; Neel R Gandhi; Joel D Ernst; Henry M Blumberg; Thomas R Ziegler
Journal:  JCI Insight       Date:  2020-05-21

Review 7.  Breast Cancer Immunotherapy: Facts and Hopes.

Authors:  Leisha A Emens
Journal:  Clin Cancer Res       Date:  2017-08-11       Impact factor: 12.531

Review 8.  [Current aspects in the prognosis of advanced melanoma].

Authors:  J Sirokay-Kohlmeyer
Journal:  Hautarzt       Date:  2018-03       Impact factor: 0.751

9.  Association of PD-L1 and IDO1 expression with JAK-STAT pathway activation in soft-tissue leiomyosarcoma.

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Journal:  J Cancer Res Clin Oncol       Date:  2020-09-20       Impact factor: 4.553

10.  Discovery of Amino-cyclobutarene-derived Indoleamine-2,3-dioxygenase 1 (IDO1) Inhibitors for Cancer Immunotherapy.

Authors:  Hongjun Zhang; Kun Liu; Qinglin Pu; Abdelghani Achab; Michael J Ardolino; Mangeng Cheng; Yongqi Deng; Amy C Doty; Heidi Ferguson; Xavier Fradera; Ian Knemeyer; Ravi Kurukulasuriya; Yu-Hong Lam; Charles A Lesburg; Theodore A Martinot; Meredeth A McGowan; J Richard Miller; Karin Otte; Purakattle J Biju; Nunzio Sciammetta; Nicolas Solban; Wensheng Yu; Hua Zhou; Xiao Wang; David Jonathan Bennett; Yongxin Han
Journal:  ACS Med Chem Lett       Date:  2019-09-18       Impact factor: 4.345

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