2018
DOI: 10.1007/s00432-017-2575-3
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MiR-29 silencing modulates the expression of target genes related to proliferation, apoptosis and methylation in Burkitt lymphoma cells

Abstract: Our results suggest a significant role for miR-29s in BL pathogenesis in altering the expression of targets involved in critical cancer pathways, such as cell cycle control, apoptosis inhibition and DNA methylation. Moreover, methylation-mediated miR-29 epigenetic silencing may occur during BL development.

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Cited by 38 publications
(35 citation statements)
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“…Cell lines and treatments. The BL cell lines: Raji (EBV + ) obtained from the American Type Culture Collection (ATCC), Daudi (EBV + ) and BL41 (EBV -) kindly provided by Dr Boulanger (Greehey Children's Cancer Research Institute, The University of Texas Health Science Center, San Antonio, TX, USA), Namalwa (EBV + ) kindly provided by Dr Favaro (Laboratório de Biologia Molecular e Celular, Hemocentro, Unicamp, Campinas, São Paulo, Brazil) and Ramos (EBV -) provided by Professor Andrei Thomas-Tikhonenko (Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA) were cultured accordingly (21). Mycoplasma contamination PCR and short tandem repeat (STR) PCR were performed to confirm that the cell lines were mycoplasma-negative and to verify their genotypes.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Cell lines and treatments. The BL cell lines: Raji (EBV + ) obtained from the American Type Culture Collection (ATCC), Daudi (EBV + ) and BL41 (EBV -) kindly provided by Dr Boulanger (Greehey Children's Cancer Research Institute, The University of Texas Health Science Center, San Antonio, TX, USA), Namalwa (EBV + ) kindly provided by Dr Favaro (Laboratório de Biologia Molecular e Celular, Hemocentro, Unicamp, Campinas, São Paulo, Brazil) and Ramos (EBV -) provided by Professor Andrei Thomas-Tikhonenko (Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA) were cultured accordingly (21). Mycoplasma contamination PCR and short tandem repeat (STR) PCR were performed to confirm that the cell lines were mycoplasma-negative and to verify their genotypes.…”
Section: Methodsmentioning
confidence: 99%
“…no. 4464058) (Life Technologies; Thermo Fisher Scientific, Inc.) utilizing the method derived from Mazzoccoli et al (21). Then, the cells were treated with decitabine (1.0 µM) and after 72 h, the cells were harvested, and miRNA was extracted and quantified as aforementioned.…”
Section: Transfection Of An Inhibitor Of Ebv-mir-bart6-5pmentioning
confidence: 99%
“…These members are encoded by two gene clusters of miR-29b2/miR-29c (mapped on chromosome 1q32) and miR-29b1/miR-29a (mapped on chromosome 7q32). 42 Heterodimer-type (Class I) PI3Ks consists of a regulatory subunit that is at least encoded by three distinct genes (85α, p85β, p55γ) and a p110 catalytic subunit. 43 The p85α is the most frequently expressed regulatory isoform of PI3K, which encodes two minor alternative splicing isoforms of p55a and p50a additionally.…”
Section: Mir-29mentioning
confidence: 99%
“…Some mutations in the seed sequence of miR-142 generated novel potential binding sites of ZEB2, a transcriptional repressor associated with EBV proliferation, and some impaired the combination of miR-142 to its targets, including RAC1 and ADCY (129). (69,131,132). Promoter hypermethylation may also induce dysregulations of lncRNA, the lower expression of lncRNA CANDE in CLL, for example (65).…”
Section: Genetic Alterationsmentioning
confidence: 99%