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1
المؤلفون: Bikfalvi, A., Da Costa, C. A., Avril, T., Barnier, J. V., Bauchet, L., Brisson, L., Cartron, P. F., Castel, H., Chevet, E., Chneiweiss, H., Clavreul, A., Constantin, B., Coronas, V., Daubon, T., Dontenwill, M., Ducray, F., Enz-Werle, N., Figarella-Branger, D., FOURNIER, Isabelle, Frenel, J. S., Gabut, M., Galli, T., Gavard, J., Huberfeld, G., Hugnot, J. P., Idbaih, A., Junier, M. P., Mathivet, T., Menei, P., Meyronet, D., Mirjolet, C., Morin, F., Mosser, J., Moyal, E. C., Rousseau, V., Salzet, Michel, Sanson, M., Seano, G., Tabouret, E., Tchoghandjian, A., Turchi, L., Vallette, F. M., Vats, S., Verreault, M., Virolle, T.
المساهمون: Université de Lille, Inserm, CHU Lille, Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM) - U1192
الوصف: Glioblastoma (GBM) is the most deadJy type of malignant brain tumor, despite extensive molecular ana y ses of GBM cens. ln recent years, the tumor microenvirc;inment (TME} has been ,recognized as an important player and therapeutic target ln GBM. However, there is a need for a full and Integrated understanding of the different cellular and molecular components involved in the GBM TME and their interactions for the development of more efficient therapies. ln this review, we provide a comprehensive report of the GBM TME, which assembles the contributions of physicians and translational researchers working on brain tumor pathology and ttierapy in France. We propose a holistic view of the subject by delineating the specifio features of the GBM TME at the cellular, molecul·ar, and therapeutic levels.
وصف الملف: application/octet-stream
العلاقة: Trends in Cancer; Trends Cancer; http://hdl.handle.net/20.500.12210/92582Test
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2دورية أكاديمية
المؤلفون: Frenel, J-S., Cartron, P-F., Gourmelon, C., Campion, L., Aumont, M., Augereau, P., Ducray, F., Loussouarn, D., Lallier, L., Robert, M., Campone, M.
المصدر: Annals of Oncology ; volume 31, page S400 ; ISSN 0923-7534
مصطلحات موضوعية: Oncology, Hematology
الإتاحة: https://doi.org/10.1016/j.annonc.2020.08.479Test
https://api.elsevier.com/content/article/PII:S0923753420404752?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0923753420404752?httpAccept=text/plainTest -
3دورية أكاديمية
المؤلفون: Asgarova, A., Asgarov, K., Godet, Y., Peixoto, P., Nadaradjane, A., Boyer-Guittaut, M., Galaine, J., Guenat, D., Mougey, V., Perrard, J., Pallandre, J. R., Bouard, A., Balland, J., Tirole, C., Adotevi, O., Hendrick, E., Herfs, M., Cartron, P. F., Borg, C., Hervouet, E.
المساهمون: Ligue Contre le Cancer, ANR
المصدر: OncoImmunology ; volume 7, issue 5, page e1423170 ; ISSN 2162-402X
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4دورية أكاديمية
المؤلفون: Morfouace, M, Lalier, L, Oliver, L, Cheray, M, Pecqueur, C, Cartron, P-F, Vallette, F M
المصدر: Cell Death & Disease ; volume 5, issue 1, page e1036-e1036 ; ISSN 2041-4889
مصطلحات موضوعية: Cancer Research, Cell Biology, Cellular and Molecular Neuroscience, Immunology
الوصف: Glioma stem cells are highly resistant to cell death and as such are supposed to contribute to tumor recurrence by eluding anticancer treatments. Here, we show that spheroids that contain rat neural stem cells (NSCs) or rat glioma stem cells (cancer stem cells, CSCs) express isoforms 1 and 2 of pyruvate kinase (PKM1 and PKM2); however, the expression of PKM2 is considerably higher in glioma spheroids. Silencing of PKM2 enhances both apoptosis and differentiation of rat and human glioma spheroids. We establish that PKM2 was implicated in glioma spheroid differentiation through its interaction with Oct4, a major regulator of self-renewal and differentiation in stem cells. The small molecule Dichloroacetate (DCA), a pyruvate dehydrogenase kinase inhibitor, increases the amount of PKM2/Oct4 complexes and thus inhibited Oct4-dependent gene expression. Taken together, our results highlight a new molecular pathway through which PKM2 can manage gliomagenesis via the control of glioma stemness by Oct4.
الإتاحة: https://doi.org/10.1038/cddis.2013.561Test
http://www.nature.com/articles/cddis2013561.pdfTest
http://www.nature.com/articles/cddis2013561Test
https://www.nature.com/articles/cddis2013561.pdfTest -
5دورية أكاديمية
المؤلفون: Cartron, P.-F., Nadaradjane, A., LePape, F., Lalier, L., Gardie, B., Vallette, F. M.
المصدر: Genes & Cancer ; volume 4, issue 5-6, page 235-241 ; ISSN 1947-6019 1947-6027
مصطلحات موضوعية: Cancer Research, Genetics
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6دورية أكاديمية
المؤلفون: Cartron, P F, Loussouarn, D, Campone, M, Martin, S A, Vallette, F M
المصدر: Cell Death & Disease ; volume 3, issue 11, page e421-e421 ; ISSN 2041-4889
مصطلحات موضوعية: Cancer Research, Cell Biology, Cellular and Molecular Neuroscience, Immunology
الإتاحة: https://doi.org/10.1038/cddis.2012.150Test
http://www.nature.com/articles/cddis2012150.pdfTest
http://www.nature.com/articles/cddis2012150Test
https://www.nature.com/articles/cddis2012150.pdfTest -
7دورية أكاديمية
المؤلفون: Gautier, F., Guillemin, Y., Cartron, P. F., Gallenne, T., Cauquil, N., Le Diguarher, T., Casara, P., Vallette, F. M., Manon, S., Hickman, J. A., Geneste, O., Juin, P.
المصدر: Molecular and Cellular Biology ; volume 31, issue 4, page 832-844 ; ISSN 1098-5549
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8دورية أكاديمية
المؤلفون: Lalier, L, Cartron, P-F, Olivier, C, Logé, C, Bougras, G, Robert, J-M, Oliver, L, Vallette, F M
المصدر: Cell Death & Differentiation ; volume 18, issue 3, page 528-537 ; ISSN 1350-9047 1476-5403
مصطلحات موضوعية: Cell Biology, Molecular Biology
الإتاحة: https://doi.org/10.1038/cdd.2010.128Test
http://www.nature.com/articles/cdd2010128.pdfTest
http://www.nature.com/articles/cdd2010128Test -
9دورية أكاديمية
المؤلفون: Hervouet, E, Vallette, F M, Cartron, P-F
المصدر: Cell Death & Disease ; volume 1, issue 1, page e8-e8 ; ISSN 2041-4889
مصطلحات موضوعية: Cancer Research, Cell Biology, Cellular and Molecular Neuroscience, Immunology
الإتاحة: https://doi.org/10.1038/cddis.2009.7Test
http://www.nature.com/articles/cddis20097.pdfTest
http://www.nature.com/articles/cddis20097Test
https://www.nature.com/articles/cddis20097.pdfTest -
10دورية أكاديمية
المؤلفون: Lalier, L, Cartron, P-F, Pedelaborde, F, Olivier, C, Loussouarn, D, Martin, S A, Meflah, K, Menanteau, J, Vallette, F M
المصدر: Oncogene ; volume 26, issue 34, page 4999-5009 ; ISSN 0950-9232 1476-5594
مصطلحات موضوعية: Cancer Research, Genetics, Molecular Biology
الإتاحة: https://doi.org/10.1038/sj.onc.1210303Test
https://www.nature.com/articles/1210303.pdfTest
https://www.nature.com/articles/1210303Test