Up-regulation of VEGF and Its Receptor in Refractory Leukemia Cells
Overview
Affiliations
Objective: To analyze the causative mechanisms in refractory leukemia cells.
Methods: Vascular endothelial growth factor (VEGF) blood plasma concentrations in 35 de novo, 6 relapse, 20 remission leukemia patients and 10 healthy kids were determined via ELISA analyses. Transcription levels of the VEGF receptors (VEGFR) Fms-like tyrosine kinase-1 (Flt-1) and kinase-domain insert containing receptor (KDR) were determined in participants' leucocytes with RT-PCR. Apoptosis rates as well as Cyt-C and Caspase-3 expression was determined in Jurkat, Jurkat(Bcl-2), healthy and recurrent leukemia leukocytes with and without VP-16 applications via flow cytometry. Total Akt (t-Akt) expression and its phosphorylation (p-AKT) status in leukocytes of the participants were analyzed with western blots.
Results: Healthy children and the remission group had the lowest blood plasma VEGF concentrations (91.16±41.34 vs. 135.80±111.28 pg/ml), followed by de novo leukemia patients (362.49±195.68 pg/ml-494.19±186.23 pg/ml) and relapse patients (574.37±278.45 pg/ml) (P<0.01). The same trend was statistically significant visible for Flt-1 and KDR expressions in leukocytes of the participants. Stable Bcl-2 overexpression led to reduced apoptosis rates as well as Cyt-C and Caspase-3 expressions in Jurkat cells after VP-16 application, which was similar in leucocytes of remission patients. In contrast to no phosphorylation in healthy children, Akt was phosphorylated in 10% remission samples, 30% de novo leukemia samples and in 67% of recurrent leukemia leucocytes.
Conclusion: High VEGF plus VEGFR expression and AKT phosphorylation are highest in leukocytes of remission patients, suggesting VEGF signaling as a cause of reduced apoptosis susceptibility upon treatments.
Iweala E, Oluwapelumi A, Dania O, Ugbogu E Life (Basel). 2023; 13(7).
PMID: 37511797 PMC: 10381774. DOI: 10.3390/life13071422.
Neuropilin (NRPs) Related Pathological Conditions and Their Modulators.
Broz M, Kolaric A, Jukic M, Bren U Int J Mol Sci. 2022; 23(15).
PMID: 35955539 PMC: 9368954. DOI: 10.3390/ijms23158402.
Shahmoradi M, Banisharif-Dehkordi F, Kouhihabibidehkordi M, Ghatrehsamani M, Jami M, Shirzad H Mol Biol Rep. 2022; 49(6):4161-4170.
PMID: 35608747 DOI: 10.1007/s11033-022-07163-0.
Chen Y, Zhang L, Zang X, Shen X, Li J, Chen L Front Pharmacol. 2022; 13:822082.
PMID: 35341213 PMC: 8948427. DOI: 10.3389/fphar.2022.822082.
Gutierrez L, Valenzuela Alvarez M, Yang Y, Spinelli F, Cantero M, Alaniz L Apoptosis. 2021; 26(7-8):447-459.
PMID: 34024019 DOI: 10.1007/s10495-021-01677-x.