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      Autophagic and Apoptotic Pathways as Targets for Chemotherapy in Glioblastoma

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          Abstract

          Glioblastoma multiforme is the most malignant and aggressive type of brain tumor, with a mean life expectancy of less than 15 months. This is due in part to the high resistance to apoptosis and moderate resistant to autophagic cell death in glioblastoma cells, and to the poor therapeutic response to conventional therapies. Autophagic cell death represents an alternative mechanism to overcome the resistance of glioblastoma to pro-apoptosis-related therapies. Nevertheless, apoptosis induction plays a major conceptual role in several experimental studies to develop novel therapies against brain tumors. In this review, we outline the different components of the apoptotic and autophagic pathways and explore the mechanisms of resistance to these cell death pathways in glioblastoma cells. Finally, we discuss drugs with clinical and preclinical use that interfere with the mechanisms of survival, proliferation, angiogenesis, migration, invasion, and cell death of malignant cells, favoring the induction of apoptosis and autophagy, or the inhibition of the latter leading to cell death, as well as their therapeutic potential in glioma, and examine new perspectives in this promising research field.

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          Most cited references276

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          AMP-activated protein kinase induces a p53-dependent metabolic checkpoint.

          Replicative cell division is an energetically demanding process that can be executed only if cells have sufficient metabolic resources to support a doubling of cell mass. Here we show that proliferating mammalian cells have a cell-cycle checkpoint that responds to glucose availability. The glucose-dependent checkpoint occurs at the G(1)/S boundary and is regulated by AMP-activated protein kinase (AMPK). This cell-cycle arrest occurs despite continued amino acid availability and active mTOR. AMPK activation induces phosphorylation of p53 on serine 15, and this phosphorylation is required to initiate AMPK-dependent cell-cycle arrest. AMPK-induced p53 activation promotes cellular survival in response to glucose deprivation, and cells that have undergone a p53-dependent metabolic arrest can rapidly reenter the cell cycle upon glucose restoration. However, persistent activation of AMPK leads to accelerated p53-dependent cellular senescence. Thus, AMPK is a cell-intrinsic regulator of the cell cycle that coordinates cellular proliferation with carbon source availability.
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            Regulation of autophagy by cytoplasmic p53.

            Multiple cellular stressors, including activation of the tumour suppressor p53, can stimulate autophagy. Here we show that deletion, depletion or inhibition of p53 can induce autophagy in human, mouse and nematode cells subjected to knockout, knockdown or pharmacological inhibition of p53. Enhanced autophagy improved the survival of p53-deficient cancer cells under conditions of hypoxia and nutrient depletion, allowing them to maintain high ATP levels. Inhibition of p53 led to autophagy in enucleated cells, and cytoplasmic, not nuclear, p53 was able to repress the enhanced autophagy of p53(-/-) cells. Many different inducers of autophagy (for example, starvation, rapamycin and toxins affecting the endoplasmic reticulum) stimulated proteasome-mediated degradation of p53 through a pathway relying on the E3 ubiquitin ligase HDM2. Inhibition of p53 degradation prevented the activation of autophagy in several cell lines, in response to several distinct stimuli. These results provide evidence of a key signalling pathway that links autophagy to the cancer-associated dysregulation of p53.
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              Brain tumors.

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                Author and article information

                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                27 November 2018
                December 2018
                : 19
                : 12
                : 3773
                Affiliations
                [1 ]Departamento de Neuroinmunología, Laboratorio de Neurobiología Molecular y Celular, Laboratorio Experimental de Enfermedades Neurodegenerativas del Instituto Nacional de Neurología y Neurocirugía “Manuel Velasco Suárez”, Ciudad de México C.P. 14269, Mexico; nasmysr@ 123456gmail.com.mx (N.S.-G.); eramed18@ 123456gmail.com (Á.E.-R.); phg6219@ 123456gmail.com (G.P.); edith.calvillo@ 123456gmail.com (M.C.); tlacaelel333@ 123456gmail.com (A.C.-S.); jsotelo@ 123456unam.mx (J.S.)
                [2 ]Hospital Regional de Alta Especialidad de Oaxaca, Secretaria de Salud, Oaxaca C.P. 71256, Mexico
                [3 ]CONACYT-Instituto Nacional de Pediatría, Secretaría de Salud, Ciudad de Mexico 04530, Mexico; racastilloro@ 123456conacyt.mx
                [4 ]Laboratorio de Inmunología, División de Estudios de Posgrado e Investigación, Facultad de Odontología, Universidad Nacional Autónoma de México, Ciudad de México C.P. 04510, Mexico; farfanmd@ 123456unam.mx
                [5 ]División Académica de Ingeniería y Arquitectura, Universidad Juárez Autónoma de Tabasco, Tabasco C.P. 86040, Mexico; mayra.alvarez@ 123456ujat.mx
                [6 ]Departamento de Cirugía Experimental, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Secretaria de Salud, Ciudad de México 14000, Mexico; atheneafloresnajera@ 123456gmail.com
                Author notes
                Author information
                https://orcid.org/0000-0002-0152-5429
                https://orcid.org/0000-0002-4883-7067
                https://orcid.org/0000-0002-1313-8872
                Article
                ijms-19-03773
                10.3390/ijms19123773
                6320836
                30486451
                41f375d8-cf55-47e6-80d2-4f9ffdd9ff7f
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 15 October 2018
                : 21 November 2018
                Categories
                Review

                Molecular biology
                glioblastoma,apoptosis,autophagia,signaling pathways,therapeutic targets,chemotherapy

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