Peroxiredoxin-2 represses NRAS-mutated melanoma cells invasion by modulating EMT markers

被引:2
|
作者
Noma, Isabella Harumi Yonehara [1 ]
Carvalho, Larissa Anastacio da Costa [1 ]
Camarena, Denisse Esther Mallaupoma [1 ]
Silva, Renaira Oliveira [1 ]
de Moraes, Manoel Oliveira [1 ]
de Souza, Sophia Tavares [1 ]
Newton-Bishop, Julia [2 ]
Nsengimana, Jeremie [3 ]
Maria-Engler, Silvya Stuchi [1 ]
机构
[1] Univ Sao Paulo, Sch Pharmaceut Sci, Dept Clin & Toxicol Anal, Ave Prof Lineu Prestes 580, BR-0550800 Sao Paulo, SP, Brazil
[2] Univ Leeds, Leeds Inst Med Res, Sch Med, Leeds LS9 7TF, England
[3] Newcastle Univ, Populat Hlth Sci Inst, Fac Med Sci, Biostat Res Grp, Newcastle Upon Tyne NE2 4BN, England
基金
巴西圣保罗研究基金会;
关键词
Cutaneous malignant melanoma; Peroxiredoxin; 2; Phenotype switching; MIGRATION; SKIN;
D O I
10.1016/j.biopha.2024.116953
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The second most common mutation in melanoma occurs in NRAS oncogene, being a more aggressive disease that has no effective approved treatment. Besides, cellular plasticity limits better outcomes of the advanced and therapy -resistant patients. Peroxiredoxins (PRDXs) control cellular processes through direct hydrogen peroxide oxidation or by redox-relaying processes. Here, we demonstrated that PRDX2 could act as a modulator of multiple EMT markers in NRAS-mutated melanomas. PRDX2 knockdown lead to phenotypic changes towards invasion in human reconstructed skin and the treatment with a PRDX mimetic (gliotoxin), decreased migration in PRDX2-deficient cells. We also confirmed the favorable clinical outcome of patients expressing PRDX2 in a large primary melanoma cohort. This study contributes to our knowledge about genes involved in phenotype switching and opens a new perspective for PRDX2 as a biomarker and target in NRAS-mutated melanomas.
引用
收藏
页数:13
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