Impact of Immune Cell Heterogeneity on HER2+ Breast Cancer Prognosis and Response to Therapy

Breast cancer is a heterogeneous disease with a high degree of diversity among and within tumors, and in relation to its different tumor microenvironment. Compared to other oncotypes, such as melanoma or lung cancer, breast cancer is considered a “cold” tumor, characterized by low T lymphocyte infil...

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Main Authors: Milena Perrone, Giovanna Talarico, Claudia Chiodoni, Sabina Sangaletti
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/13/24/6352
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author Milena Perrone
Giovanna Talarico
Claudia Chiodoni
Sabina Sangaletti
author_facet Milena Perrone
Giovanna Talarico
Claudia Chiodoni
Sabina Sangaletti
author_sort Milena Perrone
collection DOAJ
description Breast cancer is a heterogeneous disease with a high degree of diversity among and within tumors, and in relation to its different tumor microenvironment. Compared to other oncotypes, such as melanoma or lung cancer, breast cancer is considered a “cold” tumor, characterized by low T lymphocyte infiltration and low tumor mutational burden. However, more recent evidence argues against this idea and indicates that, at least for specific molecular breast cancer subtypes, the immune infiltrate may be clinically relevant and heterogeneous, with significant variations in its stromal cell/protein composition across patients and tumor stages. High numbers of tumor-infiltrating T cells are most frequent in HER2-positive and basal-like molecular subtypes and are generally associated with a good prognosis and response to therapies. However, effector immune infiltrates show protective immunity in some cancers but not in others. This could depend on one or more immunosuppressive mechanisms acting alone or in concert. Some of them might include, in addition to immune cells, other tumor microenvironment determinants such as the extracellular matrix composition and stiffness as well as stromal cells, like fibroblasts and adipocytes, that may prevent cytotoxic T cells from infiltrating the tumor microenvironment or may inactivate their antitumor functions. This review will summarize the state of the different immune tumor microenvironment determinants affecting HER2+ breast tumor progression, their response to treatment, and how they are modified by different therapeutic approaches. Potential targets within the immune tumor microenvironment will also be discussed.
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spelling doaj.art-1d2609800bf242149055463a3e5fa51f2023-11-23T04:07:32ZengMDPI AGCancers2072-66942021-12-011324635210.3390/cancers13246352Impact of Immune Cell Heterogeneity on HER2+ Breast Cancer Prognosis and Response to TherapyMilena Perrone0Giovanna Talarico1Claudia Chiodoni2Sabina Sangaletti3Molecular Immunology Unit, Department of Research, Fondazione IRCCS Istituto Nazionale Tumori, 20133 Milan, ItalyMolecular Immunology Unit, Department of Research, Fondazione IRCCS Istituto Nazionale Tumori, 20133 Milan, ItalyMolecular Immunology Unit, Department of Research, Fondazione IRCCS Istituto Nazionale Tumori, 20133 Milan, ItalyMolecular Immunology Unit, Department of Research, Fondazione IRCCS Istituto Nazionale Tumori, 20133 Milan, ItalyBreast cancer is a heterogeneous disease with a high degree of diversity among and within tumors, and in relation to its different tumor microenvironment. Compared to other oncotypes, such as melanoma or lung cancer, breast cancer is considered a “cold” tumor, characterized by low T lymphocyte infiltration and low tumor mutational burden. However, more recent evidence argues against this idea and indicates that, at least for specific molecular breast cancer subtypes, the immune infiltrate may be clinically relevant and heterogeneous, with significant variations in its stromal cell/protein composition across patients and tumor stages. High numbers of tumor-infiltrating T cells are most frequent in HER2-positive and basal-like molecular subtypes and are generally associated with a good prognosis and response to therapies. However, effector immune infiltrates show protective immunity in some cancers but not in others. This could depend on one or more immunosuppressive mechanisms acting alone or in concert. Some of them might include, in addition to immune cells, other tumor microenvironment determinants such as the extracellular matrix composition and stiffness as well as stromal cells, like fibroblasts and adipocytes, that may prevent cytotoxic T cells from infiltrating the tumor microenvironment or may inactivate their antitumor functions. This review will summarize the state of the different immune tumor microenvironment determinants affecting HER2+ breast tumor progression, their response to treatment, and how they are modified by different therapeutic approaches. Potential targets within the immune tumor microenvironment will also be discussed.https://www.mdpi.com/2072-6694/13/24/6352breast cancerHER2tumor microenvironmentimmune cellstrastuzumab
spellingShingle Milena Perrone
Giovanna Talarico
Claudia Chiodoni
Sabina Sangaletti
Impact of Immune Cell Heterogeneity on HER2+ Breast Cancer Prognosis and Response to Therapy
Cancers
breast cancer
HER2
tumor microenvironment
immune cells
trastuzumab
title Impact of Immune Cell Heterogeneity on HER2+ Breast Cancer Prognosis and Response to Therapy
title_full Impact of Immune Cell Heterogeneity on HER2+ Breast Cancer Prognosis and Response to Therapy
title_fullStr Impact of Immune Cell Heterogeneity on HER2+ Breast Cancer Prognosis and Response to Therapy
title_full_unstemmed Impact of Immune Cell Heterogeneity on HER2+ Breast Cancer Prognosis and Response to Therapy
title_short Impact of Immune Cell Heterogeneity on HER2+ Breast Cancer Prognosis and Response to Therapy
title_sort impact of immune cell heterogeneity on her2 breast cancer prognosis and response to therapy
topic breast cancer
HER2
tumor microenvironment
immune cells
trastuzumab
url https://www.mdpi.com/2072-6694/13/24/6352
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AT giovannatalarico impactofimmunecellheterogeneityonher2breastcancerprognosisandresponsetotherapy
AT claudiachiodoni impactofimmunecellheterogeneityonher2breastcancerprognosisandresponsetotherapy
AT sabinasangaletti impactofimmunecellheterogeneityonher2breastcancerprognosisandresponsetotherapy