Literature DB >> 21328335

High expression of indoleamine 2,3-dioxygenase in the tumour is associated with medullary features and favourable outcome in basal-like breast carcinoma.

Jocelyne Jacquemier1, François Bertucci, Pascal Finetti, Benjamin Esterni, Emmanuelle Charafe-Jauffret, Marie-Laure Thibult, Gilles Houvenaeghel, Benoit Van den Eynde, Daniel Birnbaum, Daniel Olive, Luc Xerri.   

Abstract

Medullary breast cancer (MBC) is a basal-like breast carcinoma (BLBC) with a favourable outcome, whereas nonmedullary BLBC has a poor prognosis. Tumour infiltrating lymphocytes (TILs) are present in both MBC and BLBC. We hypothesized that the immunosuppressive enzyme indoleamine 2,3-dioxygenase (IDO) could modulate the TILs effects among these tumours and explain their different outcomes. The amount of TILs and IDO expression were analysed using immunohistochemistry (IHC) in 155 BC cases including MBC (n = 17), atypical MBC (n = 13) and non-MBC (n = 125). Messenger RNA expression of the INDO gene, which encodes IDO, was measured in 262 cases from our institution. INDO mRNA expression and histoclinical data of 1,487 BC cases were collected from public databases. IDO immunostaining was present in both neoplastic and stromal cells in 100% of MBC and was associated with histological medullary features among non-MBC cases. There was a significant correlation between IDO positivity and TIL amounts. In our series including mostly grade-3 BC, IDO immunostaining was the most significant marker (p = 0.02) associated with better survival in multivariate analysis. Among our 262 analysed BC cases, INDO mRNA showed significant overexpression in BLBC as compared to luminal A tumours, and in MBC as compared to basal-like non-MBC. In the pooled series of 1,749 BC cases, INDO mRNA was overexpressed in BLBC and was the most significant predictor of better survival in this subtype using multivariate analysis (p = 0.0024). In conclusion, high IDO expression is associated with morphological medullary features and has an independent favourable prognostic value in BLBC.
Copyright © 2011 UICC.

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Year:  2012        PMID: 21328335     DOI: 10.1002/ijc.25979

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  40 in total

1.  IDO is highly expressed in breast cancer and breast cancer-derived circulating microvesicles and associated to aggressive types of tumors by in silico analysis.

Authors:  M T Isla Larrain; M E Rabassa; E Lacunza; A Barbera; A Cretón; A Segal-Eiras; M V Croce
Journal:  Tumour Biol       Date:  2014-04-01

2.  Promoter Methylation Modulates Indoleamine 2,3-Dioxygenase 1 Induction by Activated T Cells in Human Breast Cancers.

Authors:  Satish K Noonepalle; Franklin Gu; Eun-Joon Lee; Jeong-Hyeon Choi; Qimei Han; Jaejik Kim; Maria Ouzounova; Austin Y Shull; Lirong Pei; Pei-Yin Hsu; Ravindra Kolhe; Fang Shi; Jiseok Choi; Katie Chiou; Tim H M Huang; Hasan Korkaya; Libin Deng; Hong-Bo Xin; Shuang Huang; Muthusamy Thangaraju; Arun Sreekumar; Stefan Ambs; Shou-Ching Tang; David H Munn; Huidong Shi
Journal:  Cancer Immunol Res       Date:  2017-03-06       Impact factor: 11.151

Review 3.  Modulating Tumor Immunology by Inhibiting Indoleamine 2,3-Dioxygenase (IDO): Recent Developments and First Clinical Experiences.

Authors:  Diwakar Davar; Nathan Bahary
Journal:  Target Oncol       Date:  2018-04       Impact factor: 4.493

4.  Tryptophan metabolism in breast cancers: molecular imaging and immunohistochemistry studies.

Authors:  Csaba Juhász; Zeina Nahleh; Ian Zitron; Diane C Chugani; Majid Z Janabi; Sudeshna Bandyopadhyay; Rouba Ali-Fehmi; Thomas J Mangner; Pulak K Chakraborty; Sandeep Mittal; Otto Muzik
Journal:  Nucl Med Biol       Date:  2012-03-22       Impact factor: 2.408

5.  Suppression of indoleamine-2,3-dioxygenase 1 expression by promoter hypermethylation in ER-positive breast cancer.

Authors:  Dyah L Dewi; Soumya R Mohapatra; Saioa Blanco Cabañes; Isabell Adam; Luis F Somarribas Patterson; Bianca Berdel; Masroor Kahloon; Loreen Thürmann; Stefanie Loth; Katharina Heilmann; Dieter Weichenhan; Oliver Mücke; Ines Heiland; Pauline Wimberger; Jan Dominik Kuhlmann; Karl-Heinz Kellner; Sarah Schott; Christoph Plass; Michael Platten; Clarissa Gerhäuser; Saskia Trump; Christiane A Opitz
Journal:  Oncoimmunology       Date:  2017-01-03       Impact factor: 8.110

6.  Assessment of TILs, IDO-1, and PD-L1 in resected non-small cell lung cancer: an immunohistochemical study with clinicopathological and prognostic implications.

Authors:  Martina Mandarano; Guido Bellezza; Maria Laura Belladonna; Benoit J Van den Eynde; Rita Chiari; Jacopo Vannucci; Giada Mondanelli; Vienna Ludovini; Ivana Ferri; Fortunato Bianconi; Rachele Del Sordo; Lucio Cagini; Elisa Albini; Giulio Metro; Francesco Puma; Angelo Sidoni
Journal:  Virchows Arch       Date:  2018-11-17       Impact factor: 4.064

7.  Analysis of indoleamine 2-3 dioxygenase (IDO1) expression in breast cancer tissue by immunohistochemistry.

Authors:  Hatem Soliman; Bhupendra Rawal; Jimmy Fulp; Ji-Hyun Lee; Alexis Lopez; Marylin M Bui; Farah Khalil; Scott Antonia; Harris G Yfantis; Dong H Lee; Tiffany H Dorsey; Stefan Ambs
Journal:  Cancer Immunol Immunother       Date:  2013-01-24       Impact factor: 6.968

8.  Clinicopathologic characteristics at diagnosis and the survival of patients with medullary breast carcinoma in China: a comparison with infiltrating ductal carcinoma-not otherwise specified.

Authors:  A-Yong Cao; Min He; Liang Huang; Zhi-Ming Shao; Gen-Hong Di
Journal:  World J Surg Oncol       Date:  2013-04-22       Impact factor: 2.754

9.  The PD1/PDL1 axis, a promising therapeutic target in aggressive breast cancers.

Authors:  François Bertucci; Pascal Finetti; Daniel Birnbaum; Emilie Mamessier
Journal:  Oncoimmunology       Date:  2015-08-31       Impact factor: 8.110

Review 10.  IDO in the Tumor Microenvironment: Inflammation, Counter-Regulation, and Tolerance.

Authors:  David H Munn; Andrew L Mellor
Journal:  Trends Immunol       Date:  2016-01-31       Impact factor: 16.687

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