Metronomic Anti-Cancer Therapy: A Multimodal Therapy Governed by the Tumor Microenvironment

The concept of cancer as a systemic disease, and the therapeutic implications of this, has gained special relevance. This concept encompasses the interactions between tumor and stromal cells and their microenvironment in the complex setting of primary tumors and metastases. These factors determine c...

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Autores principales: Raquel Muñoz, Alessandra Girotti, Denise Hileeto, Francisco Javier Arias
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Lenguaje:EN
Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/90d94a6fe1d74519b9d793cd9095c4b7
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spelling oai:doaj.org-article:90d94a6fe1d74519b9d793cd9095c4b72021-11-11T15:30:43ZMetronomic Anti-Cancer Therapy: A Multimodal Therapy Governed by the Tumor Microenvironment10.3390/cancers132154142072-6694https://doaj.org/article/90d94a6fe1d74519b9d793cd9095c4b72021-10-01T00:00:00Zhttps://www.mdpi.com/2072-6694/13/21/5414https://doaj.org/toc/2072-6694The concept of cancer as a systemic disease, and the therapeutic implications of this, has gained special relevance. This concept encompasses the interactions between tumor and stromal cells and their microenvironment in the complex setting of primary tumors and metastases. These factors determine cellular co-evolution in time and space, contribute to tumor progression, and could counteract therapeutic effects. Additionally, cancer therapies can induce cellular and molecular responses in the tumor and host that allow them to escape therapy and promote tumor progression. In this study, we describe the vascular network, tumor-infiltrated immune cells, and cancer-associated fibroblasts as sources of heterogeneity and plasticity in the tumor microenvironment, and their influence on cancer progression. We also discuss tumor and host responses to the chemotherapy regimen, at the maximum tolerated dose, mainly targeting cancer cells, and a multimodal metronomic chemotherapy approach targeting both cancer cells and their microenvironment. In a combination therapy context, metronomic chemotherapy exhibits antimetastatic efficacy with low toxicity but is not exempt from resistance mechanisms. As such, a better understanding of the interactions between the components of the tumor microenvironment could improve the selection of drug combinations and schedules, as well as the use of nano-therapeutic agents against certain malignancies.Raquel MuñozAlessandra GirottiDenise HileetoFrancisco Javier AriasMDPI AGarticlemetronomic chemotherapycancer therapytumor microenvironmenttumor vascularizationbone-marrow-derived cellscancer-associated fibroblastsNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENCancers, Vol 13, Iss 5414, p 5414 (2021)
institution DOAJ
collection DOAJ
language EN
topic metronomic chemotherapy
cancer therapy
tumor microenvironment
tumor vascularization
bone-marrow-derived cells
cancer-associated fibroblasts
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle metronomic chemotherapy
cancer therapy
tumor microenvironment
tumor vascularization
bone-marrow-derived cells
cancer-associated fibroblasts
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Raquel Muñoz
Alessandra Girotti
Denise Hileeto
Francisco Javier Arias
Metronomic Anti-Cancer Therapy: A Multimodal Therapy Governed by the Tumor Microenvironment
description The concept of cancer as a systemic disease, and the therapeutic implications of this, has gained special relevance. This concept encompasses the interactions between tumor and stromal cells and their microenvironment in the complex setting of primary tumors and metastases. These factors determine cellular co-evolution in time and space, contribute to tumor progression, and could counteract therapeutic effects. Additionally, cancer therapies can induce cellular and molecular responses in the tumor and host that allow them to escape therapy and promote tumor progression. In this study, we describe the vascular network, tumor-infiltrated immune cells, and cancer-associated fibroblasts as sources of heterogeneity and plasticity in the tumor microenvironment, and their influence on cancer progression. We also discuss tumor and host responses to the chemotherapy regimen, at the maximum tolerated dose, mainly targeting cancer cells, and a multimodal metronomic chemotherapy approach targeting both cancer cells and their microenvironment. In a combination therapy context, metronomic chemotherapy exhibits antimetastatic efficacy with low toxicity but is not exempt from resistance mechanisms. As such, a better understanding of the interactions between the components of the tumor microenvironment could improve the selection of drug combinations and schedules, as well as the use of nano-therapeutic agents against certain malignancies.
format article
author Raquel Muñoz
Alessandra Girotti
Denise Hileeto
Francisco Javier Arias
author_facet Raquel Muñoz
Alessandra Girotti
Denise Hileeto
Francisco Javier Arias
author_sort Raquel Muñoz
title Metronomic Anti-Cancer Therapy: A Multimodal Therapy Governed by the Tumor Microenvironment
title_short Metronomic Anti-Cancer Therapy: A Multimodal Therapy Governed by the Tumor Microenvironment
title_full Metronomic Anti-Cancer Therapy: A Multimodal Therapy Governed by the Tumor Microenvironment
title_fullStr Metronomic Anti-Cancer Therapy: A Multimodal Therapy Governed by the Tumor Microenvironment
title_full_unstemmed Metronomic Anti-Cancer Therapy: A Multimodal Therapy Governed by the Tumor Microenvironment
title_sort metronomic anti-cancer therapy: a multimodal therapy governed by the tumor microenvironment
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/90d94a6fe1d74519b9d793cd9095c4b7
work_keys_str_mv AT raquelmunoz metronomicanticancertherapyamultimodaltherapygovernedbythetumormicroenvironment
AT alessandragirotti metronomicanticancertherapyamultimodaltherapygovernedbythetumormicroenvironment
AT denisehileeto metronomicanticancertherapyamultimodaltherapygovernedbythetumormicroenvironment
AT franciscojavierarias metronomicanticancertherapyamultimodaltherapygovernedbythetumormicroenvironment
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