Evaluation of P2X7 Receptor Function in Tumor Contexts Using rAAV Vector and Nanobodies (AAVnano)

Standard

Evaluation of P2X7 Receptor Function in Tumor Contexts Using rAAV Vector and Nanobodies (AAVnano). / Demeules, Mélanie; Scarpitta, Allan; Abad, Catalina; Gondé, Henri; Hardet, Romain; Pinto-Espinoza, Carolina; Eichhoff, Anna Marei; Schäfer, Waldemar; Haag, Friedrich; Koch-Nolte, Friedrich; Adriouch, Sahil.

in: FRONT ONCOL, Jahrgang 10, 1699, 2020.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Demeules, M, Scarpitta, A, Abad, C, Gondé, H, Hardet, R, Pinto-Espinoza, C, Eichhoff, AM, Schäfer, W, Haag, F, Koch-Nolte, F & Adriouch, S 2020, 'Evaluation of P2X7 Receptor Function in Tumor Contexts Using rAAV Vector and Nanobodies (AAVnano)', FRONT ONCOL, Jg. 10, 1699. https://doi.org/10.3389/fonc.2020.01699

APA

Demeules, M., Scarpitta, A., Abad, C., Gondé, H., Hardet, R., Pinto-Espinoza, C., Eichhoff, A. M., Schäfer, W., Haag, F., Koch-Nolte, F., & Adriouch, S. (2020). Evaluation of P2X7 Receptor Function in Tumor Contexts Using rAAV Vector and Nanobodies (AAVnano). FRONT ONCOL, 10, [1699]. https://doi.org/10.3389/fonc.2020.01699

Vancouver

Bibtex

@article{bec5197013004fd0a6f3b114bfbeb910,
title = "Evaluation of P2X7 Receptor Function in Tumor Contexts Using rAAV Vector and Nanobodies (AAVnano)",
abstract = "Adenosine triphosphate (ATP) represents a danger signal that accumulates in injured tissues, in inflammatory sites, and in the tumor microenvironment. Extracellular ATP is known to signal through plasma membrane receptors of the P2Y and P2X families. Among the P2X receptors, P2X7 has attracted increasing interest in the field of inflammation as well as in cancer. P2X7 is expressed by immune cells and by most malignant tumor cells where it plays a crucial yet complex role that remains to be clarified. P2X7 activity has been associated with production and release of pro-inflammatory cytokines, modulation of the activity and survival of immune cells, and the stimulation of proliferation and migratory properties of tumor cells. Hence, P2X7 plays an intricate role in the tumor microenvironment combining beneficial and detrimental effects that need to be further investigated. For this, we developed a novel methodology termed AAVnano based on the use of Adeno-associated viral vectors (AAV) encoding nanobodies targeting P2X7. We discuss here the advantages of this tool to study the different functions of P2X7 in cancer and other pathophysiological contexts.",
author = "M{\'e}lanie Demeules and Allan Scarpitta and Catalina Abad and Henri Gond{\'e} and Romain Hardet and Carolina Pinto-Espinoza and Eichhoff, {Anna Marei} and Waldemar Sch{\"a}fer and Friedrich Haag and Friedrich Koch-Nolte and Sahil Adriouch",
note = "Copyright {\textcopyright} 2020 Demeules, Scarpitta, Abad, Gond{\'e}, Hardet, Pinto-Espinoza, Eichhoff, Sch{\"a}fer, Haag, Koch-Nolte and Adriouch.",
year = "2020",
doi = "10.3389/fonc.2020.01699",
language = "English",
volume = "10",
journal = "FRONT ONCOL",
issn = "2234-943X",
publisher = "Frontiers Media S. A.",

}

RIS

TY - JOUR

T1 - Evaluation of P2X7 Receptor Function in Tumor Contexts Using rAAV Vector and Nanobodies (AAVnano)

AU - Demeules, Mélanie

AU - Scarpitta, Allan

AU - Abad, Catalina

AU - Gondé, Henri

AU - Hardet, Romain

AU - Pinto-Espinoza, Carolina

AU - Eichhoff, Anna Marei

AU - Schäfer, Waldemar

AU - Haag, Friedrich

AU - Koch-Nolte, Friedrich

AU - Adriouch, Sahil

N1 - Copyright © 2020 Demeules, Scarpitta, Abad, Gondé, Hardet, Pinto-Espinoza, Eichhoff, Schäfer, Haag, Koch-Nolte and Adriouch.

PY - 2020

Y1 - 2020

N2 - Adenosine triphosphate (ATP) represents a danger signal that accumulates in injured tissues, in inflammatory sites, and in the tumor microenvironment. Extracellular ATP is known to signal through plasma membrane receptors of the P2Y and P2X families. Among the P2X receptors, P2X7 has attracted increasing interest in the field of inflammation as well as in cancer. P2X7 is expressed by immune cells and by most malignant tumor cells where it plays a crucial yet complex role that remains to be clarified. P2X7 activity has been associated with production and release of pro-inflammatory cytokines, modulation of the activity and survival of immune cells, and the stimulation of proliferation and migratory properties of tumor cells. Hence, P2X7 plays an intricate role in the tumor microenvironment combining beneficial and detrimental effects that need to be further investigated. For this, we developed a novel methodology termed AAVnano based on the use of Adeno-associated viral vectors (AAV) encoding nanobodies targeting P2X7. We discuss here the advantages of this tool to study the different functions of P2X7 in cancer and other pathophysiological contexts.

AB - Adenosine triphosphate (ATP) represents a danger signal that accumulates in injured tissues, in inflammatory sites, and in the tumor microenvironment. Extracellular ATP is known to signal through plasma membrane receptors of the P2Y and P2X families. Among the P2X receptors, P2X7 has attracted increasing interest in the field of inflammation as well as in cancer. P2X7 is expressed by immune cells and by most malignant tumor cells where it plays a crucial yet complex role that remains to be clarified. P2X7 activity has been associated with production and release of pro-inflammatory cytokines, modulation of the activity and survival of immune cells, and the stimulation of proliferation and migratory properties of tumor cells. Hence, P2X7 plays an intricate role in the tumor microenvironment combining beneficial and detrimental effects that need to be further investigated. For this, we developed a novel methodology termed AAVnano based on the use of Adeno-associated viral vectors (AAV) encoding nanobodies targeting P2X7. We discuss here the advantages of this tool to study the different functions of P2X7 in cancer and other pathophysiological contexts.

U2 - 10.3389/fonc.2020.01699

DO - 10.3389/fonc.2020.01699

M3 - SCORING: Journal article

C2 - 33042812

VL - 10

JO - FRONT ONCOL

JF - FRONT ONCOL

SN - 2234-943X

M1 - 1699

ER -