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2. Sphingolipid paracrine signaling impairs keratinocyte adhesion to promote melanoma invasion

Author

Noujarède, Justine, Carrié, Lorry, Garcia, Virginie, Grimont, Maxime, Eberhardt, Anaïs, Mucher, Elodie, Genais, Matthieu, Schreuder, Anne, Carpentier, Stéphane, Ségui, Bruno, Nieto, Laurence, Levade, Thierry, Puig, Susana, Torres, Teresa, Malvehy, Josep, Harou, Olivier, Lopez, Jonathan, Dalle, Stéphane, Caramel, Julie, Gibot, Laure, Riond, Joëlle, and Andrieu-Abadie, Nathalie

Published
2023
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4. Contribution of Keratinocytes in Skin Cancer Initiation and Progression.

Author

Dainese-Marque, Océane, Garcia, Virginie, Andrieu-Abadie, Nathalie, and Riond, Joëlle

Subjects
BASAL cell carcinoma, SUNSHINE, CELL anatomy, SKIN cancer, SQUAMOUS cell carcinoma
Abstract

Keratinocytes are major cellular components of the skin and are strongly involved in its homeostasis. Oncogenic events, starting mainly from excessive sun exposure, lead to the dysregulation of their proliferation and differentiation programs and promote the initiation and progression of non-melanoma skin cancers (NMSCs). Primary melanomas, which originate from melanocytes, initiate and develop in close interaction with keratinocytes, whose role in melanoma initiation, progression, and immune escape is currently being explored. Recent studies highlighted, in particular, unexpected modes of communication between melanocytic cells and keratinocytes, which may be of interest as sources of new biomarkers in melanomagenesis or potential therapeutic targets. This review aims at reporting the various contributions of keratinocytes in skin basal cell carcinoma (BCC), cutaneous squamous cell carcinoma (cSCC), and melanoma, with a greater focus on the latter in order to highlight some recent breakthrough findings. The readers are referred to recent reviews when contextual information is needed. [ABSTRACT FROM AUTHOR]

Published
2024
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5. Ceramide metabolism alterations contribute to Tumor Necrosis Factor-induced melanoma dedifferentiation and predict resistance to immune checkpoint inhibitors in advanced melanoma patients.

Author

Dufau, Carine, Genais, Matthieu, Mucher, Elodie, Jung, Benjamin, Garcia, Virginie, Montfort, Anne, Tosolini, Marie, Clarke, Christopher J., Medin, Jeffrey A., Levade, Thierry, Delord, Jean-Pierre, Meyer, Nicolas, Pancaldi, Vera, Andrieu-Abadie, Nathalie, and Ségui, Bruno

Subjects
RNA interference, IMMUNE checkpoint inhibitors, SMALL interfering RNA, TUMOR necrosis factors, TREATMENT effectiveness, MELANOMA
Abstract

Introduction: Advanced cutaneous melanoma is a skin cancer characterized by a poor prognosis and high metastatic potential. During metastatic spread, melanoma cells often undergo dedifferentiation toward an invasive phenotype, resulting in reduced expression of microphthalmia-associated transcription factor (MITF)-dependent melanoma antigens and facilitating immune escape. Tumor Necrosis Factor (TNF) is known to be a key factor in melanoma dedifferentiation. Interestingly, accumulating evidence suggests that TNF may play a role in melanoma progression and resistance to immunotherapies. Additionally, TNF has been identified as a potent regulator of sphingolipid metabolism, which could contribute to melanoma aggressiveness and the process of melanoma dedifferentiation. Methods: We conducted RNA sequencing and mass spectrometry analyses to investigate TNF-induced dedifferentiation in two melanoma cell lines. In vitro experiments were performed to manipulate sphingolipid metabolism using genetic or pharmacologic alterations in combination with TNF treatment, aiming to elucidate the potential involvement of this metabolism in TNF-induced dedifferentiation. Lastly, to evaluate the clinical significance of our findings, we performed unsupervised analysis of plasma sphingolipid levels in 48 patients receiving treatment with immune checkpoint inhibitors, either alone or in combination with anti-TNF therapy. Results: Herein, we demonstrate that TNF-induced melanoma cell dedifferentiation is associated with a global modulation of sphingolipid metabolism. Specifically, TNF decreases the expression and activity of acid ceramidase (AC), encoded by the ASAH1 gene, while increasing the expression of glucosylceramide synthase (GCS), encoded by the UGCG gene. Remarkably, knockdown of AC alone via RNA interference is enough to induce melanoma cell dedifferentiation. Furthermore, treatment with Eliglustat, a GCS inhibitor, inhibits TNF-induced melanoma cell dedifferentiation. Lastly, analysis of plasma samples from patients treated with immune checkpoint inhibitors, with or without anti-TNF therapy, revealed significant predictive sphingolipids. Notably, the top 8 predictive sphingolipids, including glycosphingolipids, were associated with a poor response to immunotherapy. Discussion: Our study highlights that ceramide metabolism alterations are causally involved in TNF-induced melanoma cell dedifferentiation and suggests that the evolution of specific ceramide metabolites in plasma may be considered as predictive biomarkers of resistance to immunotherapy. [ABSTRACT FROM AUTHOR]

Published
2024
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6. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Author

Klionsky, Daniel J, Abdelmohsen, Kotb, Abe, Akihisa, Abedin, Md Joynal, Abeliovich, Hagai, Acevedo Arozena, Abraham, Adachi, Hiroaki, Adams, Christopher M, Adams, Peter D, Adeli, Khosrow, Adhihetty, Peter J, Adler, Sharon G, Agam, Galila, Agarwal, Rajesh, Aghi, Manish K, Agnello, Maria, Agostinis, Patrizia, Aguilar, Patricia V, Aguirre-Ghiso, Julio, Airoldi, Edoardo M, Ait-Si-Ali, Slimane, Akematsu, Takahiko, Akporiaye, Emmanuel T, Al-Rubeai, Mohamed, Albaiceta, Guillermo M, Albanese, Chris, Albani, Diego, Albert, Matthew L, Aldudo, Jesus, Algül, Hana, Alirezaei, Mehrdad, Alloza, Iraide, Almasan, Alexandru, Almonte-Beceril, Maylin, Alnemri, Emad S, Alonso, Covadonga, Altan-Bonnet, Nihal, Altieri, Dario C, Alvarez, Silvia, Alvarez-Erviti, Lydia, Alves, Sandro, Amadoro, Giuseppina, Amano, Atsuo, Amantini, Consuelo, Ambrosio, Santiago, Amelio, Ivano, Amer, Amal O, Amessou, Mohamed, Amon, Angelika, An, Zhenyi, Anania, Frank A, Andersen, Stig U, Andley, Usha P, Andreadi, Catherine K, Andrieu-Abadie, Nathalie, Anel, Alberto, Ann, David K, Anoopkumar-Dukie, Shailendra, Antonioli, Manuela, Aoki, Hiroshi, Apostolova, Nadezda, Aquila, Saveria, Aquilano, Katia, Araki, Koichi, Arama, Eli, Aranda, Agustin, Araya, Jun, Arcaro, Alexandre, Arias, Esperanza, Arimoto, Hirokazu, Ariosa, Aileen R, Armstrong, Jane L, Arnould, Thierry, Arsov, Ivica, Asanuma, Katsuhiko, Askanas, Valerie, Asselin, Eric, Atarashi, Ryuichiro, Atherton, Sally S, Atkin, Julie D, Attardi, Laura D, Auberger, Patrick, Auburger, Georg, Aurelian, Laure, Autelli, Riccardo, Avagliano, Laura, Avantaggiati, Maria Laura, Avrahami, Limor, Awale, Suresh, Azad, Neelam, Bachetti, Tiziana, Backer, Jonathan M, Bae, Dong-Hun, Bae, Jae-Sung, Bae, Ok-Nam, Bae, Soo Han, Baehrecke, Eric H, Baek, Seung-Hoon, Baghdiguian, Stephen, and Bagniewska-Zadworna, Agnieszka

Subjects
Biochemistry and Cell Biology, Biological Sciences, Animals, Autophagy, Biological Assay, Computer Simulation, Humans, autolysosome, autophagosome, chaperone-mediated autophagy, flux, LC3, lysosome, macroautophagy, phagophore, stress, vacuole, Biochemistry & Molecular Biology, Biochemistry and cell biology
Published
2016

9. Lysosomal acid ceramidase ASAH1 controls the transition between invasive and proliferative phenotype in melanoma cells

Author

Leclerc, Justine, Garandeau, David, Pandiani, Charlotte, Gaudel, Céline, Bille, Karine, Nottet, Nicolas, Garcia, Virginie, Colosetti, Pascal, Pagnotta, Sophie, Bahadoran, Philippe, Tondeur, Garance, Mograbi, Baharia, Dalle, Stéphane, Caramel, Julie, Levade, Thierry, Ballotti, Robert, Andrieu-Abadie, Nathalie, and Bertolotto, Corine

Published
2019
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10. Guidelines for the use and interpretation of assays for monitoring autophagy.

Author

Klionsky, Daniel J, Abdalla, Fabio C, Abeliovich, Hagai, Abraham, Robert T, Acevedo-Arozena, Abraham, Adeli, Khosrow, Agholme, Lotta, Agnello, Maria, Agostinis, Patrizia, Aguirre-Ghiso, Julio A, Ahn, Hyung Jun, Ait-Mohamed, Ouardia, Ait-Si-Ali, Slimane, Akematsu, Takahiko, Akira, Shizuo, Al-Younes, Hesham M, Al-Zeer, Munir A, Albert, Matthew L, Albin, Roger L, Alegre-Abarrategui, Javier, Aleo, Maria Francesca, Alirezaei, Mehrdad, Almasan, Alexandru, Almonte-Becerril, Maylin, Amano, Atsuo, Amaravadi, Ravi, Amarnath, Shoba, Amer, Amal O, Andrieu-Abadie, Nathalie, Anantharam, Vellareddy, Ann, David K, Anoopkumar-Dukie, Shailendra, Aoki, Hiroshi, Apostolova, Nadezda, Arancia, Giuseppe, Aris, John P, Asanuma, Katsuhiko, Asare, Nana YO, Ashida, Hisashi, Askanas, Valerie, Askew, David S, Auberger, Patrick, Baba, Misuzu, Backues, Steven K, Baehrecke, Eric H, Bahr, Ben A, Bai, Xue-Yuan, Bailly, Yannick, Baiocchi, Robert, Baldini, Giulia, Balduini, Walter, Ballabio, Andrea, Bamber, Bruce A, Bampton, Edward TW, Bánhegyi, Gábor, Bartholomew, Clinton R, Bassham, Diane C, Bast, Robert C, Batoko, Henri, Bay, Boon-Huat, Beau, Isabelle, Béchet, Daniel M, Begley, Thomas J, Behl, Christian, Behrends, Christian, Bekri, Soumeya, Bellaire, Bryan, Bendall, Linda J, Benetti, Luca, Berliocchi, Laura, Bernardi, Henri, Bernassola, Francesca, Besteiro, Sébastien, Bhatia-Kissova, Ingrid, Bi, Xiaoning, Biard-Piechaczyk, Martine, Blum, Janice S, Boise, Lawrence H, Bonaldo, Paolo, Boone, David L, Bornhauser, Beat C, Bortoluci, Karina R, Bossis, Ioannis, Bost, Frédéric, Bourquin, Jean-Pierre, Boya, Patricia, Boyer-Guittaut, Michaël, Bozhkov, Peter V, Brady, Nathan R, Brancolini, Claudio, Brech, Andreas, Brenman, Jay E, Brennand, Ana, Bresnick, Emery H, Brest, Patrick, Bridges, Dave, Bristol, Molly L, Brookes, Paul S, Brown, Eric J, and Brumell, John H

Subjects
Animals, Humans, Biological Assay, Models, Biological, Autophagy, Generic health relevance, autolysosome, autophagosome, flux, LC3, lysosome, phagophore, stress, vacuole, Biochemistry and Cell Biology, Biochemistry & Molecular Biology
Abstract

In 2008 we published the first set of guidelines for standardizing research in autophagy. Since then, research on this topic has continued to accelerate, and many new scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Accordingly, it is important to update these guidelines for monitoring autophagy in different organisms. Various reviews have described the range of assays that have been used for this purpose. Nevertheless, there continues to be confusion regarding acceptable methods to measure autophagy, especially in multicellular eukaryotes. A key point that needs to be emphasized is that there is a difference between measurements that monitor the numbers or volume of autophagic elements (e.g., autophagosomes or autolysosomes) at any stage of the autophagic process vs. those that measure flux through the autophagy pathway (i.e., the complete process); thus, a block in macroautophagy that results in autophagosome accumulation needs to be differentiated from stimuli that result in increased autophagic activity, defined as increased autophagy induction coupled with increased delivery to, and degradation within, lysosomes (in most higher eukaryotes and some protists such as Dictyostelium) or the vacuole (in plants and fungi). In other words, it is especially important that investigators new to the field understand that the appearance of more autophagosomes does not necessarily equate with more autophagy. In fact, in many cases, autophagosomes accumulate because of a block in trafficking to lysosomes without a concomitant change in autophagosome biogenesis, whereas an increase in autolysosomes may reflect a reduction in degradative activity. Here, we present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes. These guidelines are not meant to be a formulaic set of rules, because the appropriate assays depend in part on the question being asked and the system being used. In addition, we emphasize that no individual assay is guaranteed to be the most appropriate one in every situation, and we strongly recommend the use of multiple assays to monitor autophagy. In these guidelines, we consider these various methods of assessing autophagy and what information can, or cannot, be obtained from them. Finally, by discussing the merits and limits of particular autophagy assays, we hope to encourage technical innovation in the field.

Published
2012

11. Resistance of melanoma to immune checkpoint inhibitors is overcome by targeting the sphingosine kinase-1

Author

Imbert, Caroline, Montfort, Anne, Fraisse, Marine, Marcheteau, Elie, Gilhodes, Julia, Martin, Elodie, Bertrand, Florie, Marcellin, Marlène, Burlet-Schiltz, Odile, Peredo, Anne Gonzalez de, Garcia, Virginie, Carpentier, Stéphane, Tartare-Deckert, Sophie, Brousset, Pierre, Rochaix, Philippe, Puisset, Florent, Filleron, Thomas, Meyer, Nicolas, Lamant, Laurence, Levade, Thierry, Ségui, Bruno, Andrieu-Abadie, Nathalie, and Colacios, Céline

Published
2020
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15. Data from Neutral Sphingomyelinase 2 Heightens Anti-Melanoma Immune Responses and Anti–PD-1 Therapy Efficacy

Author

Montfort, Anne, primary, Bertrand, Florie, primary, Rochotte, Julia, primary, Gilhodes, Julia, primary, Filleron, Thomas, primary, Milhès, Jean, primary, Dufau, Carine, primary, Imbert, Caroline, primary, Riond, Joëlle, primary, Tosolini, Marie, primary, Clarke, Christopher J., primary, Dufour, Florent, primary, Constantinescu, Andrei A., primary, Junior, Nilton De França, primary, Garcia, Virginie, primary, Record, Michel, primary, Cordelier, Pierre, primary, Brousset, Pierre, primary, Rochaix, Philippe, primary, Silvente-Poirot, Sandrine, primary, Therville, Nicole, primary, Andrieu-Abadie, Nathalie, primary, Levade, Thierry, primary, Hannun, Yusuf A., primary, Benoist, Hervé, primary, Meyer, Nicolas, primary, Micheau, Olivier, primary, Colacios, Céline, primary, and Ségui, Bruno, primary

Published
2023
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16. Supplementary Data File S1 from Neutral Sphingomyelinase 2 Heightens Anti-Melanoma Immune Responses and Anti–PD-1 Therapy Efficacy

Author

Montfort, Anne, primary, Bertrand, Florie, primary, Rochotte, Julia, primary, Gilhodes, Julia, primary, Filleron, Thomas, primary, Milhès, Jean, primary, Dufau, Carine, primary, Imbert, Caroline, primary, Riond, Joëlle, primary, Tosolini, Marie, primary, Clarke, Christopher J., primary, Dufour, Florent, primary, Constantinescu, Andrei A., primary, Junior, Nilton De França, primary, Garcia, Virginie, primary, Record, Michel, primary, Cordelier, Pierre, primary, Brousset, Pierre, primary, Rochaix, Philippe, primary, Silvente-Poirot, Sandrine, primary, Therville, Nicole, primary, Andrieu-Abadie, Nathalie, primary, Levade, Thierry, primary, Hannun, Yusuf A., primary, Benoist, Hervé, primary, Meyer, Nicolas, primary, Micheau, Olivier, primary, Colacios, Céline, primary, and Ségui, Bruno, primary

Published
2023
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17. Supplementary Tables and Figures from Neutral Sphingomyelinase 2 Heightens Anti-Melanoma Immune Responses and Anti–PD-1 Therapy Efficacy

Author

Montfort, Anne, primary, Bertrand, Florie, primary, Rochotte, Julia, primary, Gilhodes, Julia, primary, Filleron, Thomas, primary, Milhès, Jean, primary, Dufau, Carine, primary, Imbert, Caroline, primary, Riond, Joëlle, primary, Tosolini, Marie, primary, Clarke, Christopher J., primary, Dufour, Florent, primary, Constantinescu, Andrei A., primary, Junior, Nilton De França, primary, Garcia, Virginie, primary, Record, Michel, primary, Cordelier, Pierre, primary, Brousset, Pierre, primary, Rochaix, Philippe, primary, Silvente-Poirot, Sandrine, primary, Therville, Nicole, primary, Andrieu-Abadie, Nathalie, primary, Levade, Thierry, primary, Hannun, Yusuf A., primary, Benoist, Hervé, primary, Meyer, Nicolas, primary, Micheau, Olivier, primary, Colacios, Céline, primary, and Ségui, Bruno, primary

Published
2023
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18. Supplementary Data from Targeting the Sphingosine 1-Phosphate Axis Exerts Potent Antitumor Activity in BRAFi-Resistant Melanomas

Author

Garandeau, David, primary, Noujarède, Justine, primary, Leclerc, Justine, primary, Imbert, Caroline, primary, Garcia, Virginie, primary, Bats, Marie-Lise, primary, Rambow, Florian, primary, Gilhodes, Julia, primary, Filleron, Thomas, primary, Meyer, Nicolas, primary, Brayer, Stéphanie, primary, Arcucci, Silvia, primary, Tartare-Deckert, Sophie, primary, Ségui, Bruno, primary, Marine, Jean-Christophe, primary, Levade, Thierry, primary, Bertolotto, Corine, primary, and Andrieu-Abadie, Nathalie, primary

Published
2023
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19. Supplementary Figure S3 from Targeting the Sphingosine 1-Phosphate Axis Exerts Potent Antitumor Activity in BRAFi-Resistant Melanomas

Author

Garandeau, David, primary, Noujarède, Justine, primary, Leclerc, Justine, primary, Imbert, Caroline, primary, Garcia, Virginie, primary, Bats, Marie-Lise, primary, Rambow, Florian, primary, Gilhodes, Julia, primary, Filleron, Thomas, primary, Meyer, Nicolas, primary, Brayer, Stéphanie, primary, Arcucci, Silvia, primary, Tartare-Deckert, Sophie, primary, Ségui, Bruno, primary, Marine, Jean-Christophe, primary, Levade, Thierry, primary, Bertolotto, Corine, primary, and Andrieu-Abadie, Nathalie, primary

Published
2023
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20. Supplementary information from Blocking Tumor Necrosis Factor α Enhances CD8 T-cell–Dependent Immunity in Experimental Melanoma

Author

Bertrand, Florie, primary, Rochotte, Julia, primary, Colacios, Céline, primary, Montfort, Anne, primary, Tilkin-Mariamé, Anne-Françoise, primary, Touriol, Christian, primary, Rochaix, Philippe, primary, Lajoie-Mazenc, Isabelle, primary, Andrieu-Abadie, Nathalie, primary, Levade, Thierry, primary, Benoist, Hervé, primary, and Ségui, Bruno, primary

Published
2023
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21. Supplementary Figure S5 from Blocking Tumor Necrosis Factor α Enhances CD8 T-cell–Dependent Immunity in Experimental Melanoma

Author

Bertrand, Florie, primary, Rochotte, Julia, primary, Colacios, Céline, primary, Montfort, Anne, primary, Tilkin-Mariamé, Anne-Françoise, primary, Touriol, Christian, primary, Rochaix, Philippe, primary, Lajoie-Mazenc, Isabelle, primary, Andrieu-Abadie, Nathalie, primary, Levade, Thierry, primary, Benoist, Hervé, primary, and Ségui, Bruno, primary

Published
2023
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22. Data from Disruption of Sphingosine 1-Phosphate Lyase Confers Resistance to Chemotherapy and Promotes Oncogenesis through Bcl-2/Bcl-xL Upregulation

Author

Colié, Sandra, primary, Van Veldhoven, Paul P., primary, Kedjouar, Blandine, primary, Bedia, Carmen, primary, Albinet, Virginie, primary, Sorli, Sonia-Caroline, primary, Garcia, Virginie, primary, Djavaheri-Mergny, Mojgan, primary, Bauvy, Chantal, primary, Codogno, Patrice, primary, Levade, Thierry, primary, and Andrieu-Abadie, Nathalie, primary

Published
2023
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23. Supplementary Materials, Figures 1-5 from Disruption of Sphingosine 1-Phosphate Lyase Confers Resistance to Chemotherapy and Promotes Oncogenesis through Bcl-2/Bcl-xL Upregulation

Author

Colié, Sandra, primary, Van Veldhoven, Paul P., primary, Kedjouar, Blandine, primary, Bedia, Carmen, primary, Albinet, Virginie, primary, Sorli, Sonia-Caroline, primary, Garcia, Virginie, primary, Djavaheri-Mergny, Mojgan, primary, Bauvy, Chantal, primary, Codogno, Patrice, primary, Levade, Thierry, primary, and Andrieu-Abadie, Nathalie, primary

Published
2023
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30. PARKIN Inactivation Links Parkinson’s Disease to Melanoma

Author

Hu, Hui-Han, Kannengiesser, Caroline, Lesage, Suzanne, André, Jocelyne, Mourah, Samia, Michel, Laurence, Descamps, Vincent, Basset-Seguin, Nicole, Bagot, Martine, Bensussan, Armand, Lebbé, Céleste, Deschamps, Lydia, Saiag, Philippe, Leccia, Marie-Thérèse, Bressac-de-Paillerets, Brigitte, Tsalamlal, Amel, Kumar, Rajiv, Klebe, Stephan, Grandchamp, Bernard, Andrieu-Abadie, Nathalie, Thomas, Luc, Brice, Alexis, Dumaz, Nicolas, and Soufir, Nadem

Published
2016
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34. Neutral Sphingomyelinase 2 Heightens Anti-Melanoma Immune Responses and Anti–PD-1 Therapy Efficacy

Author

Montfort, Anne, primary, Bertrand, Florie, additional, Rochotte, Julia, additional, Gilhodes, Julia, additional, Filleron, Thomas, additional, Milhès, Jean, additional, Dufau, Carine, additional, Imbert, Caroline, additional, Riond, Joëlle, additional, Tosolini, Marie, additional, Clarke, Christopher J., additional, Dufour, Florent, additional, Constantinescu, Andrei A., additional, Junior, Nilton De França, additional, Garcia, Virginie, additional, Record, Michel, additional, Cordelier, Pierre, additional, Brousset, Pierre, additional, Rochaix, Philippe, additional, Silvente-Poirot, Sandrine, additional, Therville, Nicole, additional, Andrieu-Abadie, Nathalie, additional, Levade, Thierry, additional, Hannun, Yusuf A., additional, Benoist, Hervé, additional, Meyer, Nicolas, additional, Micheau, Olivier, additional, Colacios, Céline, additional, and Ségui, Bruno, additional

Published
2021
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35. Combining Nivolumab and Ipilimumab with Infliximab or Certolizumab in Patients with Advanced Melanoma: First Results of a Phase Ib Clinical Trial

Author

Montfort, Anne, primary, Filleron, Thomas, additional, Virazels, Mathieu, additional, Dufau, Carine, additional, Milhès, Jean, additional, Pagès, Cécile, additional, Olivier, Pascale, additional, Ayyoub, Maha, additional, Mounier, Muriel, additional, Lusque, Amélie, additional, Brayer, Stéphanie, additional, Delord, Jean-Pierre, additional, Andrieu-Abadie, Nathalie, additional, Levade, Thierry, additional, Colacios, Céline, additional, Ségui, Bruno, additional, and Meyer, Nicolas, additional

Published
2021
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36. Genetic Disorders of Simple Sphingolipid Metabolism

Author

Albinet, Virginie, primary, Bats, Marie-Lise, additional, Bedia, Carmen, additional, Sabourdy, Frédérique, additional, Garcia, Virginie, additional, Ségui, Bruno, additional, Andrieu-Abadie, Nathalie, additional, Hornemann, Thorsten, additional, and Levade, Thierry, additional

Published
2013
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45. Corrigendum: The TNF Paradox in Cancer Progression and Immunotherapy

Author

Montfort, Anne, Colacios, Céline, Levade, Thierry, Andrieu-Abadie, Nathalie, Meyer, Nicolas, and Ségui, Bruno

Subjects
Opinion, Tumor Necrosis Factor-alpha, Immunology, immune escape, Correction, tumor necrosis factor (TNF), PD-1, melanoma, Animals, Humans, Immunology and Allergy, CTLA-4, Immunotherapy, Neoplasm Metastasis
Published
2019
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46. Ceramide in Apoptosis

Author

Ségui, Bruno, primary, Cuvillier, Olivier, additional, Malagarie-Cazenave, Sophie, additional, Lévêque, Sophie, additional, Gouazé, Valérie, additional, Andrieu-Abadie, Nathalie, additional, and Levade, Thierry, additional

Published
2002
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