Publication: Advancements in synthetic biology-based bacterial cancer therapy: A modular design approach.
| dc.contributor.author | Arboleda-García, Andrés | |
| dc.contributor.author | Alarcón-Ruiz, Iván | |
| dc.contributor.author | Boada-Acosta, Lissette | |
| dc.contributor.author | Boada, Yadira | |
| dc.contributor.author | Vignoni, Alejandro | |
| dc.contributor.author | Jantus-Lewintre, Eloisa | |
| dc.contributor.funder | Centro de Investigación Biomédica en Red - CIBERONC (Cáncer) | es_ES |
| dc.contributor.funder | Ministerio de Ciencia e Innovación (España) | es_ES |
| dc.date.accessioned | 2024-02-09T15:39:15Z | |
| dc.date.available | 2024-02-09T15:39:15Z | |
| dc.date.issued | 2023-10 | |
| dc.description.abstract | Synthetic biology aims to program living bacteria cells with artificial genetic circuits for user-defined functions, transforming them into powerful tools with numerous applications in various fields, including oncology. Cancer treatments have serious side effects on patients due to the systemic action of the drugs involved. To address this, new systems that provide localized antitumoral action while minimizing damage to healthy tissues are required. Bacteria, often considered pathogenic agents, have been used as cancer treatments since the early 20th century. Advances in genetic engineering, synthetic biology, microbiology, and oncology have improved bacterial therapies, making them safer and more effective. Here we propose six modules for a successful synthetic biology-based bacterial cancer therapy, the modules include Payload, Release, Tumor-targeting, Biocontainment, Memory, and Genetic Circuit Stability Module. These will ensure antitumor activity, safety for the environment and patient, prevent bacterial colonization, maintain cell stability, and prevent loss or defunctionalization of the genetic circuit. | es_ES |
| dc.description.peerreviewed | Sí | es_ES |
| dc.description.sponsorship | This research was funded by MCIN/AEI/10.13039/501100011033 Grant numbers PID2020-117271RB-C21 and TED2021-131049B-I00, Generalitat Valenciana GVA Grant CIAICO/2021/159, Centro de Investigacion ´ Biom´edica en Red de Cancer ´ (CIBERONC) Grant CB16-12- 00350, Instituto de Salud Carlos III (Grant PI22/01221), and GVA Grant AICO/2021/333. A Arboleda-García thanks the Grant PAID-01–21 Programa de Ayudas de Investigacion ´ y Desarrollo from Universitat Polit`ecnica de Val`encia, Spain. I Alarcon-Ruiz thanks the FPU grant (FPU20/04814) from the Spanish Government. L Boada-Acosta thanks the Grant Santiago Grisolía GRISOLIAP/2021/030 from Conselleria de Innovacion, ´ Universidades, Ciencia y Sociedad Digital and Generalitat Valenciana, Spain. Y Boada is thankful for the Grant PAID-10-21 Acceso al Sistema Espanol ˜ de Ciencia e Innovacion ´ from Universitat Polit`ecnica de Val`encia, Spain; and the Scholarship Convocatoria Abierta 2011 from Secretaría de Educacion ´ Superior, Ciencia, Tecnología e Innovacion, ´ Ecuador. The authors are grateful to Prof. Jesús Pico ´ for his guidance during the preparation of this manuscript. BioRender was used to illustrate the figures under a paid license for publication authorization. | es_ES |
| dc.format.page | 104088 | es_ES |
| dc.format.volume | 190 | es_ES |
| dc.identifier.citation | Crit Rev Oncol Hematol. 2023 Oct:190:104088. | es_ES |
| dc.identifier.doi | 10.1016/j.critrevonc.2023.104088 | es_ES |
| dc.identifier.e-issn | 1879-0461 | es_ES |
| dc.identifier.journal | Critical reviews in oncology/hematology | es_ES |
| dc.identifier.pubmedID | 37541537 | es_ES |
| dc.identifier.uri | http://hdl.handle.net/20.500.12105/17710 | |
| dc.language.iso | eng | es_ES |
| dc.publisher | Elsevier | es_ES |
| dc.relation.projectFECYT | info:eu-repo/grantAgreement/ES/MCIN/AEI/10.13039/501100011033 | es_ES |
| dc.relation.projectFECYT | info:eu-repo/grantAgreement/ES/PID2020-117271RB-C21 | es_ES |
| dc.relation.projectFECYT | info:eu-repo/grantAgreement/ES/TED2021-131049B-I00 | es_ES |
| dc.relation.projectFECYT | info:eu-repo/grantAgreement/ES/CIAICO/2021/159 | es_ES |
| dc.relation.projectFECYT | info:eu-repo/grantAgreement/ES/FPU20/04814 | es_ES |
| dc.relation.projectFECYT | info:eu-repo/grantAgreement/ES/GRISOLIAP/2021/030 | es_ES |
| dc.relation.projectFECYT | info:eu-repo/grantAgreement/ES/PAID-10-21 | es_ES |
| dc.relation.publisherversion | 10.1016/j.critrevonc.2023.104088 | es_ES |
| dc.repisalud.institucion | CNIC | es_ES |
| dc.repisalud.orgCNIC | CNIC::Grupos de investigación::Genética Funcional del Sistema de Fosforilación Oxidativa | es_ES |
| dc.rights.accessRights | open access | es_ES |
| dc.rights.license | Attribution-NonCommercial-NoDerivatives 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
| dc.subject.mesh | Synthetic Biology | es_ES |
| dc.subject.mesh | Neoplasms | es_ES |
| dc.subject.mesh | Humans | es_ES |
| dc.subject.mesh | Genetic Engineering | es_ES |
| dc.subject.mesh | Bacteria | es_ES |
| dc.subject.mesh | Gene Regulatory Networks | es_ES |
| dc.title | Advancements in synthetic biology-based bacterial cancer therapy: A modular design approach. | es_ES |
| dc.type | journal article | es_ES |
| dc.type.hasVersion | AM | es_ES |
| dspace.entity.type | Publication |
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