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Cell Death Mechanisms Induced by CLytA-DAAO Chimeric Enzyme in Human Tumor Cell Lines

Authors :
P. Garcia-Morales
Maria Fuentes-Baile
Miguel Saceda
Víctor Manuel Barberá
Camino de Juan Romero
Elizabeth Pérez-Valenciano
María Paz Ventero
Cristina Alenda
Jesús Sanz
Instituto de Salud Carlos III
Asociación de Mujeres afectadas por Cáncer de mama de Elche y comarca
Ministerio de Economía, Industria y Competitividad (España)
Consejo Superior de Investigaciones Científicas (España)
Fuentes-Baile, María [0000-0003-3653-2407]
Ventero, María Paz [0000-0003-1979-0949]
Sanz, Jesús M. [0000-0002-4421-9376]
de Juan Romero, Camino [0000-0001-7890-8447]
Barberá, Victor M. [0000-0002-4012-6973]
Alenda, Cristina [0000-0002-0560-1759]
Saceda, Miguel [0000-0002-1564-3602]
Fuentes-Baile, María
Ventero, María Paz
Sanz, Jesús M.
de Juan Romero, Camino
Barberá, Victor M.
Alenda, Cristina
Saceda, Miguel
Source :
International Journal of Molecular Sciences, Volume 21, Issue 22, Digital.CSIC. Repositorio Institucional del CSIC, instname, International Journal of Molecular Sciences, Vol 21, Iss 8522, p 8522 (2020)
Publication Year :
2020
Publisher :
Multidisciplinary Digital Publishing Institute, 2020.

Abstract

23 p.-11 fig.<br />The combination of the choline binding domain of the amidase N-acetylmuramoyl-L-alanine (CLytA)-D-amino acid oxidase (DAAO) (CLytA-DAAO) and D-Alanine induces cell death in several pancreatic and colorectal carcinoma and glioblastoma cell lines. In glioblastoma cell lines, CLytA-DAAO-induced cell death was inhibited by a pan-caspase inhibitor, suggesting a classical apoptotic cell death. Meanwhile, the cell death induced in pancreatic and colon carcinoma cell lines is some type of programmed necrosis. In this article, we studied the mechanisms that trigger CLytA-DAAO-induced cell death in pancreatic and colorectal carcinoma and glioblastoma cell lines and we acquire a further insight into the necrotic cell death induced in pancreatic and colorectal carcinoma cell lines. We have analyzed the intracellular calcium mobilization, mitochondrial membrane potential, PARP-1 participation and AIF translocation. Although the mitochondrial membrane depolarization plays a crucial role, our results suggest that CLytA-DAAO-induced cell death is context dependent. We have previously detected pancreatic and colorectal carcinoma cell lines (Hs766T and HT-29, respectively) that were resistant to CLytA-DAAO-induced cell death. In this study, we have examined the putative mechanism underlying the resistance in these cell lines, evaluating both detoxification mechanisms and the inflammatory and survival responses. Overall, our results provide a better understanding on the cell death mechanism induced by CLytA-DAAO, a promising therapy against cancer.<br />This research was funded by Spanish Instituto de Salud Carlos III, grant number PI01202025, and donations from Association of women affected by breast cancer in Elche and the region (AMACMEC) to M.S., Miguel Servet Program from Instituto de Salud Carlos III (CP19/00095) to C.d.J.R. and grants from the Spanish Ministry of Economy, Industry and Competitiveness, grant numbers BIO2013-47684-R and BIO2016-79323-R, and the RETICS-FEDER RICET, RD16/0027/0010, to J.M.S. The CIBER of Enfermedades Respiratorias (CIBERES) is an initiative of the Spanish Instituto de Salud Carlos III and Spanish National Research Council (CSIC Grant 201820I132).

Details

Language :
English
ISSN :
14220067
Database :
OpenAIRE
Journal :
International Journal of Molecular Sciences
Accession number :
edsair.doi.dedup.....7b1b9fd42644309ba80a1ffacf53eb03
Full Text :
https://doi.org/10.3390/ijms21228522