Cargando…
Development of a VLP-Based Vaccine Displaying an xCT Extracellular Domain for the Treatment of Metastatic Breast Cancer
Metastatic breast cancer (MBC) is the leading cause of cancer death in women due to recurrence and resistance to conventional therapies. Thus, MBC represents an important unmet clinical need for new treatments. In this paper we generated a virus-like particle (VLP)-based vaccine (AX09) to inhibit de...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352461/ https://www.ncbi.nlm.nih.gov/pubmed/32521631 http://dx.doi.org/10.3390/cancers12061492 |
_version_ | 1783557643499995136 |
---|---|
author | Rolih, Valeria Caldeira, Jerri Bolli, Elisabetta Salameh, Ahmad Conti, Laura Barutello, Giuseppina Riccardo, Federica Magri, Jolanda Lamolinara, Alessia Parra, Karla Valenzuela, Paloma Francia, Giulio Iezzi, Manuela Pericle, Federica Cavallo, Federica |
author_facet | Rolih, Valeria Caldeira, Jerri Bolli, Elisabetta Salameh, Ahmad Conti, Laura Barutello, Giuseppina Riccardo, Federica Magri, Jolanda Lamolinara, Alessia Parra, Karla Valenzuela, Paloma Francia, Giulio Iezzi, Manuela Pericle, Federica Cavallo, Federica |
author_sort | Rolih, Valeria |
collection | PubMed |
description | Metastatic breast cancer (MBC) is the leading cause of cancer death in women due to recurrence and resistance to conventional therapies. Thus, MBC represents an important unmet clinical need for new treatments. In this paper we generated a virus-like particle (VLP)-based vaccine (AX09) to inhibit de novo metastasis formation and ultimately prolong the survival of patients with MBC. To this aim, we engineered the bacteriophage MS2 VLP to display an extracellular loop of xCT, a promising therapeutic target involved in tumor progression and metastasis formation. Elevated levels of this protein are observed in a high percentage of invasive mammary ductal tumors including triple negative breast cancer (TNBC) and correlate with poor overall survival. Moreover, xCT expression is restricted to only a few normal cell types. Here, we tested AX09 in several MBC mouse models and showed that it was well-tolerated and elicited a strong antibody response against xCT. This antibody-based response resulted in the inhibition of xCT’s function in vitro and reduced metastasis formation in vivo. Thus, AX09 represents a promising novel approach for MBC, and it is currently advancing to clinical development. |
format | Online Article Text |
id | pubmed-7352461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73524612020-07-15 Development of a VLP-Based Vaccine Displaying an xCT Extracellular Domain for the Treatment of Metastatic Breast Cancer Rolih, Valeria Caldeira, Jerri Bolli, Elisabetta Salameh, Ahmad Conti, Laura Barutello, Giuseppina Riccardo, Federica Magri, Jolanda Lamolinara, Alessia Parra, Karla Valenzuela, Paloma Francia, Giulio Iezzi, Manuela Pericle, Federica Cavallo, Federica Cancers (Basel) Article Metastatic breast cancer (MBC) is the leading cause of cancer death in women due to recurrence and resistance to conventional therapies. Thus, MBC represents an important unmet clinical need for new treatments. In this paper we generated a virus-like particle (VLP)-based vaccine (AX09) to inhibit de novo metastasis formation and ultimately prolong the survival of patients with MBC. To this aim, we engineered the bacteriophage MS2 VLP to display an extracellular loop of xCT, a promising therapeutic target involved in tumor progression and metastasis formation. Elevated levels of this protein are observed in a high percentage of invasive mammary ductal tumors including triple negative breast cancer (TNBC) and correlate with poor overall survival. Moreover, xCT expression is restricted to only a few normal cell types. Here, we tested AX09 in several MBC mouse models and showed that it was well-tolerated and elicited a strong antibody response against xCT. This antibody-based response resulted in the inhibition of xCT’s function in vitro and reduced metastasis formation in vivo. Thus, AX09 represents a promising novel approach for MBC, and it is currently advancing to clinical development. MDPI 2020-06-08 /pmc/articles/PMC7352461/ /pubmed/32521631 http://dx.doi.org/10.3390/cancers12061492 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Rolih, Valeria Caldeira, Jerri Bolli, Elisabetta Salameh, Ahmad Conti, Laura Barutello, Giuseppina Riccardo, Federica Magri, Jolanda Lamolinara, Alessia Parra, Karla Valenzuela, Paloma Francia, Giulio Iezzi, Manuela Pericle, Federica Cavallo, Federica Development of a VLP-Based Vaccine Displaying an xCT Extracellular Domain for the Treatment of Metastatic Breast Cancer |
title | Development of a VLP-Based Vaccine Displaying an xCT Extracellular Domain for the Treatment of Metastatic Breast Cancer |
title_full | Development of a VLP-Based Vaccine Displaying an xCT Extracellular Domain for the Treatment of Metastatic Breast Cancer |
title_fullStr | Development of a VLP-Based Vaccine Displaying an xCT Extracellular Domain for the Treatment of Metastatic Breast Cancer |
title_full_unstemmed | Development of a VLP-Based Vaccine Displaying an xCT Extracellular Domain for the Treatment of Metastatic Breast Cancer |
title_short | Development of a VLP-Based Vaccine Displaying an xCT Extracellular Domain for the Treatment of Metastatic Breast Cancer |
title_sort | development of a vlp-based vaccine displaying an xct extracellular domain for the treatment of metastatic breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352461/ https://www.ncbi.nlm.nih.gov/pubmed/32521631 http://dx.doi.org/10.3390/cancers12061492 |
work_keys_str_mv | AT rolihvaleria developmentofavlpbasedvaccinedisplayinganxctextracellulardomainforthetreatmentofmetastaticbreastcancer AT caldeirajerri developmentofavlpbasedvaccinedisplayinganxctextracellulardomainforthetreatmentofmetastaticbreastcancer AT bollielisabetta developmentofavlpbasedvaccinedisplayinganxctextracellulardomainforthetreatmentofmetastaticbreastcancer AT salamehahmad developmentofavlpbasedvaccinedisplayinganxctextracellulardomainforthetreatmentofmetastaticbreastcancer AT contilaura developmentofavlpbasedvaccinedisplayinganxctextracellulardomainforthetreatmentofmetastaticbreastcancer AT barutellogiuseppina developmentofavlpbasedvaccinedisplayinganxctextracellulardomainforthetreatmentofmetastaticbreastcancer AT riccardofederica developmentofavlpbasedvaccinedisplayinganxctextracellulardomainforthetreatmentofmetastaticbreastcancer AT magrijolanda developmentofavlpbasedvaccinedisplayinganxctextracellulardomainforthetreatmentofmetastaticbreastcancer AT lamolinaraalessia developmentofavlpbasedvaccinedisplayinganxctextracellulardomainforthetreatmentofmetastaticbreastcancer AT parrakarla developmentofavlpbasedvaccinedisplayinganxctextracellulardomainforthetreatmentofmetastaticbreastcancer AT valenzuelapaloma developmentofavlpbasedvaccinedisplayinganxctextracellulardomainforthetreatmentofmetastaticbreastcancer AT franciagiulio developmentofavlpbasedvaccinedisplayinganxctextracellulardomainforthetreatmentofmetastaticbreastcancer AT iezzimanuela developmentofavlpbasedvaccinedisplayinganxctextracellulardomainforthetreatmentofmetastaticbreastcancer AT periclefederica developmentofavlpbasedvaccinedisplayinganxctextracellulardomainforthetreatmentofmetastaticbreastcancer AT cavallofederica developmentofavlpbasedvaccinedisplayinganxctextracellulardomainforthetreatmentofmetastaticbreastcancer |