Breast cancer is a highly heterogeneous disease, at both inter- and intra-tumor levels, and this heterogeneity is a crucial determinant of malignant progression and response to treatments. In addition to genetic diversity and plasticity of cancer cells, the tumor microenvironment contributes to tumor heterogeneity shaping the physical and biological surroundings of the tumor. The activity of certain types of immune, endothelial or mesenchymal cells in the microenvironment can change the effectiveness of cancer therapies via a plethora of different mechanisms. Therefore, deciphering the interactions between the distinct cell types, their spatial organization and their specific contribution to tumor growth and drug sensitivity is still a major challenge. Dissecting intra-tumor heterogeneity is currently an urgent need to better define breast cancer biology and to develop therapeutic strategies targeting the microenvironment as helpful tools for combined and personalized treatment. In this review, we analyze the mechanisms by which the tumor microenvironment affects the characteristics of tumor heterogeneity that ultimately result in drug resistance, and we outline state of the art preclinical models and emerging technologies that will be instrumental in unraveling the impact of the tumor microenvironment on resistance to therapies.

The role of tumor microenvironment in drug resistance: emerging technologies to unravel breast cancer heterogeneity

Salemme, Vincenzo;Centonze, Giorgia;Avalle, Lidia;Natalini, Dora;Arina, Pietro;Morellato, Alessandro;Ala, Ugo;Taverna, Daniela;Defilippi, Paola
2023-01-01

Abstract

Breast cancer is a highly heterogeneous disease, at both inter- and intra-tumor levels, and this heterogeneity is a crucial determinant of malignant progression and response to treatments. In addition to genetic diversity and plasticity of cancer cells, the tumor microenvironment contributes to tumor heterogeneity shaping the physical and biological surroundings of the tumor. The activity of certain types of immune, endothelial or mesenchymal cells in the microenvironment can change the effectiveness of cancer therapies via a plethora of different mechanisms. Therefore, deciphering the interactions between the distinct cell types, their spatial organization and their specific contribution to tumor growth and drug sensitivity is still a major challenge. Dissecting intra-tumor heterogeneity is currently an urgent need to better define breast cancer biology and to develop therapeutic strategies targeting the microenvironment as helpful tools for combined and personalized treatment. In this review, we analyze the mechanisms by which the tumor microenvironment affects the characteristics of tumor heterogeneity that ultimately result in drug resistance, and we outline state of the art preclinical models and emerging technologies that will be instrumental in unraveling the impact of the tumor microenvironment on resistance to therapies.
2023
Inglese
Esperti anonimi
13
1170264
1170285
22
https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2023.1170264/full
breast cancer; cancer heterogenicity; drug resistance; molecular mechanisms; tumor microenvironment
REGNO UNITO DI GRAN BRETAGNA
   Functional role of the adaptor protein p140cap in breast cancer: molecular mechanisms and tumor sensitivity to therapy
   DEFP_AIRC_22
   FONDAZIONE AIRC PER LA RICERCA SUL CANCRO
   Progetto IG 2022 ID 27353

   Ruolo dell'oncosoppressore p140Cap nella risposta alle terapie farmacologiche nel tumore mammario
   p140TFTM
   FONDAZIONE CRT
   Cod. ROL 73249 - RF= 2020.1798

   National Center for Gene Therapy and Drugs based on RNA Technology
   CN-RNA
   Ministero dell'Università e della Ricerca
   OLIVIERO S. - PNRR - Centri Nazionali (CN)
1 – prodotto con file in versione Open Access (allegherò il file al passo 6 - Carica)
11
03-CONTRIBUTO IN RIVISTA::03B-Review in Rivista / Rassegna della Lett. in Riv. / Nota Critica
open
262
info:eu-repo/semantics/article
Salemme, Vincenzo; Centonze, Giorgia; Avalle, Lidia; Natalini, Dora; Piccolantonio, Alessio; Arina, Pietro; Morellato, Alessandro; Ala, Ugo; Taverna, ...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1927552
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