Zobrazeno 1 - 10
of 37
pro vyhledávání: '"MESH: Melanoma, Experimental"'
Autor:
Anthime Flaus, Vincent Habouzit, Nicolas de Leiris, Jean-Philippe Vuillez, Marie-Thérèse Leccia, Mathilde Simonson, Jean-Luc Perrot, Florent Cachin, Nathalie Prevot
Publikováno v:
American Journal of Cancer Research
American Journal of Cancer Research, 2022, 12 (3), pp.1116-1128. ⟨10.3390/diagnostics12020388⟩
Diagnostics
Diagnostics, MDPI, 2022, 12 (2), pp.388. ⟨10.3390/diagnostics12020388⟩
American Journal of Cancer Research, e-Century Publishing, 2022, 12 (3), pp.1116-1128. ⟨10.3390/diagnostics12020388⟩
Diagnostics; Volume 12; Issue 2; Pages: 388
American Journal of Cancer Research, 2022, 12 (3), pp.1116-1128. ⟨10.3390/diagnostics12020388⟩
Diagnostics
Diagnostics, MDPI, 2022, 12 (2), pp.388. ⟨10.3390/diagnostics12020388⟩
American Journal of Cancer Research, e-Century Publishing, 2022, 12 (3), pp.1116-1128. ⟨10.3390/diagnostics12020388⟩
Diagnostics; Volume 12; Issue 2; Pages: 388
International audience; An increasing number of studies concerning solid cancers, including prostate cancer, are tending to demonstrate the predominant role of the interactions of tumor cells with their microenvironment, and underlining the relevance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da55e27547f0a152934851e54fea0029
https://hal.science/hal-03863669
https://hal.science/hal-03863669
Autor:
Vincent Caval, J Thalmensi, T Bestetti, E Pliquet, L Fiette, M Julithe, T. Huet, Anna Kostrzak, M Escande, Simon Wain-Hobson, Pierre Langlade-Demoyen
Publikováno v:
Gene Therapy
Gene Therapy, Nature Publishing Group, 2017, 24 (2), pp.74-83. ⟨10.1038/gt.2016.77⟩
Gene Therapy, 2017, 24 (2), pp.74-83. ⟨10.1038/gt.2016.77⟩
Gene Therapy, Nature Publishing Group, 2017, 24 (2), pp.74-83. ⟨10.1038/gt.2016.77⟩
Gene Therapy, 2017, 24 (2), pp.74-83. ⟨10.1038/gt.2016.77⟩
International audience; Human APOBEC3A (A3A) cytidine deaminase shows pro-apoptotic properties resulting from hypermutation of genomic DNA, induction of double-stranded DNA breaks (DSBs) and G1 cell cycle arrest. Given this, we evaluated the antitumo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8487b68fc1c4afe01c1197b742d10a6
https://hal-pasteur.archives-ouvertes.fr/pasteur-02545771
https://hal-pasteur.archives-ouvertes.fr/pasteur-02545771
Autor:
Laurent Baud, Guillaume Hanouna, Joëlle Perez, Jean-Philippe Haymann, Emmanuel Letavernier, Sophie Vandermeersch, Ellie Tang
Publikováno v:
Journal of Investigative Dermatology
Journal of Investigative Dermatology, 2020, 140 (2), pp.445-454. ⟨10.1016/j.jid.2019.06.148⟩
Journal of Investigative Dermatology, Nature Publishing Group, 2020, 140 (2), pp.445-454. ⟨10.1016/j.jid.2019.06.148⟩
Journal of Investigative Dermatology, 2020, 140 (2), pp.445-454. ⟨10.1016/j.jid.2019.06.148⟩
Journal of Investigative Dermatology, Nature Publishing Group, 2020, 140 (2), pp.445-454. ⟨10.1016/j.jid.2019.06.148⟩
International audience; Calpains, intracellular proteases specifically inhibited by calpastatin, play a major role in neoangiogenesis involved in tumor invasiveness and metastasis. They are partly exteriorized via the ATP-binding cassette transporter
Autor:
François Ghiringhelli, Narcisse Zwetyenga, Naim Akhtar Khan, Kabirou Moutairou, Françoise Salvadori, Aziz Hichami, Akadiri Yessoufou
Publikováno v:
Biochimie
Biochimie, Elsevier, 2016, 131, pp.1-10. 〈http://www.sciencedirect.com/science/article/pii/S0300908416301687〉. 〈10.1016/j.biochi.2016.09.001〉
Biochimie, Elsevier, 2016, 131, pp.1-10. ⟨10.1016/j.biochi.2016.09.001⟩
Biochimie, Elsevier, 2016, 131, pp.1-10. 〈http://www.sciencedirect.com/science/article/pii/S0300908416301687〉. 〈10.1016/j.biochi.2016.09.001〉
Biochimie, Elsevier, 2016, 131, pp.1-10. ⟨10.1016/j.biochi.2016.09.001⟩
International audience; Regulatory T (Treg) cells are important to induce and maintain immunological self-tolerance. Although the progress accomplished in understanding the functional mechanism of Treg cells, intracellular molecules that control the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::680a88628c39b4f4606d36c13f1ca7cc
https://hal-univ-bourgogne.archives-ouvertes.fr/hal-01452771
https://hal-univ-bourgogne.archives-ouvertes.fr/hal-01452771
Autor:
James P. Di Santo, Pierre Bruhns, Laurence Fiette, Friederike Jönsson, David A. Mancardi, Clifford A. Lowell, Bruno Iannascoli, Marcello Albanesi
Publikováno v:
Blood
Blood, American Society of Hematology, 2013, 122 (18), pp.3160-3164. ⟨10.1182/blood-2013-04-497446⟩
Blood, 2013, 122 (18), pp.3160-3164. ⟨10.1182/blood-2013-04-497446⟩
Blood, American Society of Hematology, 2013, 122 (18), pp.3160-3164. ⟨10.1182/blood-2013-04-497446⟩
Blood, 2013, 122 (18), pp.3160-3164. ⟨10.1182/blood-2013-04-497446⟩
International audience; Tumor engraftment followed by monoclonal antibody (mAb) therapy targeting tumor antigens represents a gold standard for assessing the efficiency of mAbs to eliminate tumor cells. Mouse models have demonstrated that receptors f
Stress from Nucleotide Depletion Activates the Transcriptional Regulator HEXIM1 to Suppress Melanoma
Autor:
Alvaro C. Laga, John M. Asara, Howard Y. Chang, Justin L. Tan, Brian T. Do, Leonard I. Zon, Anne Bothmer, Richard M. White, David H. Price, Ng Shyh-Chang, Ryan A. Flynn, Nicole Pandell, Song Yang, Violaine Saint-André, Yoon Jung Kim, Zi Peng Fan, Koh Fujinaga, Elliott J. Hagedorn, Serine Avagyan, Tae Hoon Kim, Cristina Santoriello, B. Matija Peterlin, Ellen van Rooijen, John G. Clohessy, John E. Brogie, Richard A. Young, Celeste B. Greer, Yi Zhou, Pier Paolo Pandolfi, Rachel D. Fogley, Julien Ablain
Publikováno v:
Molecular Cell
Molecular Cell, 2016, 62 (1), pp.34-46. ⟨10.1016/j.molcel.2016.03.013⟩
Molecular Cell, Elsevier, 2016, 62 (1), pp.34-46. ⟨10.1016/j.molcel.2016.03.013⟩
PMC
Molecular cell, vol 62, iss 1
Molecular Cell, 2016, 62 (1), pp.34-46. ⟨10.1016/j.molcel.2016.03.013⟩
Molecular Cell, Elsevier, 2016, 62 (1), pp.34-46. ⟨10.1016/j.molcel.2016.03.013⟩
PMC
Molecular cell, vol 62, iss 1
International audience; Studying cancer metabolism gives insight into tumorigenic survival mechanisms and susceptibilities. In melanoma, we identify HEXIM1, a transcription elongation regulator, as a melanoma tumor suppressor that responds to nucleot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d2be414500e23e7e55cf569d834dacf
https://hal-pasteur.archives-ouvertes.fr/pasteur-02871949
https://hal-pasteur.archives-ouvertes.fr/pasteur-02871949
Autor:
Pierre Bruhns, Andrew J. Murphy, Marcello Albanesi, Laurence Zitvogel, Jeanette H. W. Leusen, Bruno Iannascoli, David A. Mancardi, Macdonald Lynn
Publikováno v:
Journal of Immunology
Journal of Immunology, Publisher : Baltimore : Williams & Wilkins, c1950-. Latest Publisher : Bethesda, MD : American Association of Immunologists, 2012, 189 (12), pp.5513-5517. ⟨10.4049/jimmunol.1201511⟩
Journal of Immunology, 2012, 189 (12), pp.5513-5517. ⟨10.4049/jimmunol.1201511⟩
Journal of Immunology, Publisher : Baltimore : Williams & Wilkins, c1950-. Latest Publisher : Bethesda, MD : American Association of Immunologists, 2012, 189 (12), pp.5513-5517. ⟨10.4049/jimmunol.1201511⟩
Journal of Immunology, 2012, 189 (12), pp.5513-5517. ⟨10.4049/jimmunol.1201511⟩
Erratum in J Immunol. 2013 Feb 1;190(3):1381. Daëron, Marc [added].; International audience; mAb therapy for experimental metastatic melanoma relies on activating receptors for the Fc portion of IgG (FcγR). Opposing results on the respective contri
Autor:
Grégoire Mignot, Alice Hervieu, Cédric Rébé, Lionel Apetoh, Frédérique Végran, Fanny Chalmin, François Ghiringhelli, Mélanie Bruchard, Pierre Vabres
Publikováno v:
Journal of Investigative Dermatology
Journal of Investigative Dermatology, Nature Publishing Group, 2013, 133 (2), pp.499-508. ⟨10.1038/jid.2012.273⟩
Journal of Investigative Dermatology, 2013, 133 (2), pp.499-508. ⟨10.1038/jid.2012.273⟩
Journal of Investigative Dermatology, Nature Publishing Group, 2013, 133 (2), pp.499-508. 〈10.1038/jid.2012.273〉
Journal of Investigative Dermatology, Nature Publishing Group, 2013, 133 (2), pp.499-508. ⟨10.1038/jid.2012.273⟩
Journal of Investigative Dermatology, 2013, 133 (2), pp.499-508. ⟨10.1038/jid.2012.273⟩
Journal of Investigative Dermatology, Nature Publishing Group, 2013, 133 (2), pp.499-508. 〈10.1038/jid.2012.273〉
International audience; Dacarbazine (DTIC) is a cytotoxic drug widely used for melanoma treatment. However, the putative contribution of anticancer immune responses in the efficacy of DTIC has not been evaluated. By testing how DTIC affects host immu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8bb5bff821678b5ff52126169d6f5f9
https://www.hal.inserm.fr/inserm-00857892
https://www.hal.inserm.fr/inserm-00857892
Autor:
Esther Tarrab, Alain Lamarre, Marie-Pierre Langlois, Valérie Janelle, Laurent Poliquin, Pascal Lapierre
Publikováno v:
Cancer Immunology Research
Cancer Immunology Research, American Association for Cancer Research, 2014, 2 (3), pp.200-206. ⟨10.1158/2326-6066.CIR-13-0173⟩
Cancer Immunology Research, American Association for Cancer Research, 2014, 2 (3), pp.200-206. ⟨10.1158/2326-6066.CIR-13-0173⟩
Although the role of the complement system in cancer development has been studied, its involvement in the development of an antitumoral immune response remains poorly understood. Using cobra venom factor (CVF) to inhibit the complement cascade via C3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4da392e5050477bd687beca6bcad80d
https://hal.archives-ouvertes.fr/hal-01199024/document
https://hal.archives-ouvertes.fr/hal-01199024/document
Autor:
Pedro Berraondo, Nico van Rooijen, Ángeles Domínguez-Soto, Mateo de las Casas-Engel, Carmen Sánchez-Torres, David Sancho, Rafael Bragado, Laura Aragoneses-Fenoll, María L. Toribio, José Medina-Echeverz, Silvia Sánchez-Ramón, Pierre Bruhns, María A. Moro, Antonio Castrillo, Angel L. Corbí, Isabel Cuartero, Enrique Martin-Gayo
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Journal of Immunology
Journal of Immunology, Publisher : Baltimore : Williams & Wilkins, c1950-. Latest Publisher : Bethesda, MD : American Association of Immunologists, 2014, 193 (10), pp.5181-5189. ⟨10.4049/jimmunol.1303375⟩
Journal of Immunology, 2014, 193 (10), pp.5181-5189. ⟨10.4049/jimmunol.1303375⟩
Dominguez-Soto, A, de las Casas-Engel, M, Bragado, R, Medina-Echeverz, J, ragoneses-Fenoll, L, Martin-Gayo, E, van Rooijen, N, Berraondo, P, Toribio, M L, Moro, M A, Cuartero, I, Castrillo, A, Sancho, D, Sanchez-Torres, C, Bruhns, P, Sanchez-Ramon, S & Corbi, A L 2014, ' Intravenous Immunoglobulin Promotes Antitumor Responses by Modulating Macrophage Polarization ', Journal of Immunology, vol. 193, no. 10, pp. 5181-5189 . https://doi.org/10.4049/jimmunol.1303375
Journal of Immunology, 193(10), 5181-5189. American Association of Immunologists
instname
Journal of Immunology
Journal of Immunology, Publisher : Baltimore : Williams & Wilkins, c1950-. Latest Publisher : Bethesda, MD : American Association of Immunologists, 2014, 193 (10), pp.5181-5189. ⟨10.4049/jimmunol.1303375⟩
Journal of Immunology, 2014, 193 (10), pp.5181-5189. ⟨10.4049/jimmunol.1303375⟩
Dominguez-Soto, A, de las Casas-Engel, M, Bragado, R, Medina-Echeverz, J, ragoneses-Fenoll, L, Martin-Gayo, E, van Rooijen, N, Berraondo, P, Toribio, M L, Moro, M A, Cuartero, I, Castrillo, A, Sancho, D, Sanchez-Torres, C, Bruhns, P, Sanchez-Ramon, S & Corbi, A L 2014, ' Intravenous Immunoglobulin Promotes Antitumor Responses by Modulating Macrophage Polarization ', Journal of Immunology, vol. 193, no. 10, pp. 5181-5189 . https://doi.org/10.4049/jimmunol.1303375
Journal of Immunology, 193(10), 5181-5189. American Association of Immunologists
et al.
Intravenous Igs (IVIg) therapy is widely used as an immunomodulatory strategy in inflammatory pathologies and is suggested to promote cancer regression. Because progression of tumors depends on their ability to redirect the polarization s
Intravenous Igs (IVIg) therapy is widely used as an immunomodulatory strategy in inflammatory pathologies and is suggested to promote cancer regression. Because progression of tumors depends on their ability to redirect the polarization s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::566460992fa0cc83ffac0d36922cda3a
http://hdl.handle.net/10261/124545
http://hdl.handle.net/10261/124545