New potential antiproliferative monophosphoester 2-aminoethyl dihydrogen phosphate in K-562 and K-562 MDR+ leukemia cells

The main obstacle in the treatment of cancer patients has been resistance to multiple drugs, leading to the need to develop molecules with a higher specificity target. The liposomal formulation DODAC/2-AEH2P has antitumor potential, inducing apoptosis in several tumor types. Human chronic myeloid le...

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Main Authors: TO. Conceição, LGS. Cabral, MG. Laveli-Silva, JC. Pacheco, MG. Alves, DC. Rabelo, RAN. Laiso, DA. Maria
Format: Article
Language:English
Published: Elsevier 2021-10-01
Series:Biomedicine & Pharmacotherapy
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0753332221008374
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spelling doaj-fcead2b78a054295a3cde6e23ac003602021-09-19T04:54:34ZengElsevierBiomedicine & Pharmacotherapy0753-33222021-10-01142112054New potential antiproliferative monophosphoester 2-aminoethyl dihydrogen phosphate in K-562 and K-562 MDR+ leukemia cellsTO. Conceição0LGS. Cabral1MG. Laveli-Silva2JC. Pacheco3MG. Alves4DC. Rabelo5RAN. Laiso6DA. Maria7Faculty of Medicine, University of Sao Paulo, FMUSP, Sao Paulo, SP, Brazil; Laboratory of Development and Innovation, Butantan Institute, Sao Paulo, SP, BrazilFaculty of Medicine, University of Sao Paulo, FMUSP, Sao Paulo, SP, Brazil; Laboratory of Development and Innovation, Butantan Institute, Sao Paulo, SP, BrazilFaculty of Medicine, University of Sao Paulo, FMUSP, Sao Paulo, SP, Brazil; Laboratory of Development and Innovation, Butantan Institute, Sao Paulo, SP, BrazilFaculty of Medicine, University of Sao Paulo, FMUSP, Sao Paulo, SP, Brazil; Laboratory of Development and Innovation, Butantan Institute, Sao Paulo, SP, BrazilFaculty of Medicine, University of Sao Paulo, FMUSP, Sao Paulo, SP, Brazil; Laboratory of Development and Innovation, Butantan Institute, Sao Paulo, SP, BrazilFaculty of Medicine, University of Sao Paulo, FMUSP, Sao Paulo, SP, BrazilLaboratory of Development and Innovation, Butantan Institute, Sao Paulo, SP, BrazilFaculty of Medicine, University of Sao Paulo, FMUSP, Sao Paulo, SP, Brazil; Laboratory of Development and Innovation, Butantan Institute, Sao Paulo, SP, Brazil; Corresponding author at: Faculty of Medicine, University of Sao Paulo, FMUSP, Sao Paulo, SP, Brazil.The main obstacle in the treatment of cancer patients has been resistance to multiple drugs, leading to the need to develop molecules with a higher specificity target. The liposomal formulation DODAC/2-AEH2P has antitumor potential, inducing apoptosis in several tumor types. Human chronic myeloid leukemia K-562 and K-562 Lucena (MDR+) cells were treated with the DODAC carrier and the liposomal formulation 2-AEH2P. Viability, cell cycle phases, apoptosis, marker expression and mitochondrial potential were analyzed. Significant reduction in viability was observed for all treatments. Changes in the distribution of the cell cycle phases and expression of markers involved in the apoptosis pathways were observed. Reduction of the mitochondrial electrical potential mediated by Bcl-2, being regulated by the reduction of the MTCH2 protein linked to the progression of myeloid leukemia and an increase in the pro-apoptotic proteins Bad and Bax, dependent on p53. This study demonstrated a significant therapeutic potential through apoptotic effects in leukemic cells, regardless of the molecular resistance profile (MDR+).http://www.sciencedirect.com/science/article/pii/S0753332221008374LeukemiaDrug resistanceDODAC carrierLiposomal formulation2-AEH2P
collection DOAJ
language English
format Article
sources DOAJ
author TO. Conceição
LGS. Cabral
MG. Laveli-Silva
JC. Pacheco
MG. Alves
DC. Rabelo
RAN. Laiso
DA. Maria
spellingShingle TO. Conceição
LGS. Cabral
MG. Laveli-Silva
JC. Pacheco
MG. Alves
DC. Rabelo
RAN. Laiso
DA. Maria
New potential antiproliferative monophosphoester 2-aminoethyl dihydrogen phosphate in K-562 and K-562 MDR+ leukemia cells
Biomedicine & Pharmacotherapy
Leukemia
Drug resistance
DODAC carrier
Liposomal formulation
2-AEH2P
author_facet TO. Conceição
LGS. Cabral
MG. Laveli-Silva
JC. Pacheco
MG. Alves
DC. Rabelo
RAN. Laiso
DA. Maria
author_sort TO. Conceição
title New potential antiproliferative monophosphoester 2-aminoethyl dihydrogen phosphate in K-562 and K-562 MDR+ leukemia cells
title_short New potential antiproliferative monophosphoester 2-aminoethyl dihydrogen phosphate in K-562 and K-562 MDR+ leukemia cells
title_full New potential antiproliferative monophosphoester 2-aminoethyl dihydrogen phosphate in K-562 and K-562 MDR+ leukemia cells
title_fullStr New potential antiproliferative monophosphoester 2-aminoethyl dihydrogen phosphate in K-562 and K-562 MDR+ leukemia cells
title_full_unstemmed New potential antiproliferative monophosphoester 2-aminoethyl dihydrogen phosphate in K-562 and K-562 MDR+ leukemia cells
title_sort new potential antiproliferative monophosphoester 2-aminoethyl dihydrogen phosphate in k-562 and k-562 mdr+ leukemia cells
publisher Elsevier
series Biomedicine & Pharmacotherapy
issn 0753-3322
publishDate 2021-10-01
description The main obstacle in the treatment of cancer patients has been resistance to multiple drugs, leading to the need to develop molecules with a higher specificity target. The liposomal formulation DODAC/2-AEH2P has antitumor potential, inducing apoptosis in several tumor types. Human chronic myeloid leukemia K-562 and K-562 Lucena (MDR+) cells were treated with the DODAC carrier and the liposomal formulation 2-AEH2P. Viability, cell cycle phases, apoptosis, marker expression and mitochondrial potential were analyzed. Significant reduction in viability was observed for all treatments. Changes in the distribution of the cell cycle phases and expression of markers involved in the apoptosis pathways were observed. Reduction of the mitochondrial electrical potential mediated by Bcl-2, being regulated by the reduction of the MTCH2 protein linked to the progression of myeloid leukemia and an increase in the pro-apoptotic proteins Bad and Bax, dependent on p53. This study demonstrated a significant therapeutic potential through apoptotic effects in leukemic cells, regardless of the molecular resistance profile (MDR+).
topic Leukemia
Drug resistance
DODAC carrier
Liposomal formulation
2-AEH2P
url http://www.sciencedirect.com/science/article/pii/S0753332221008374
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