Advanced search
Start date
Betweenand
(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Loss of 5 `-Methylthioadenosine Phosphorylase (MTAP) is Frequent in High-Grade Gliomas; Nevertheless, it is Not Associated with Higher Tumor Aggressiveness

Full text
Author(s):
Show less -
de Menezes, Weder Pereira [1] ; Oliveira Silva, Viviane Aline [1] ; Faria Gomes, Izabela Natalia [1] ; Rosa, Marcela Nunes [1] ; Corcoll Spina, Maria Luisa [1] ; Carloni, Adriana Cruvinel [1] ; Vieira Alves, Ana Laura [1] ; Melendez, Matias [1] ; Almeida, Gisele Caravina [2] ; da Silva, Luciane Sussuchi [1] ; Clara, Carlos [3] ; da Cunha, Isabela Werneck [4] ; Maroso Hajj, Glaucia Noeli [4] ; Jones, Chris [5] ; Bidinotto, Lucas Tadeu [1, 6, 7] ; Reis, Rui Manuel [1, 8, 9]
Total Authors: 16
Affiliation:
[1] Barretos Canc Hosp, Mol Oncol Res Ctr, BR-14784400 Barretos, SP - Brazil
[2] Barretos Canc Hosp, Dept Pathol, BR-14784400 Barretos, SP - Brazil
[3] Barretos Canc Hosp, Dept Neurosurg, BR-14784400 Barretos, SP - Brazil
[4] AC Camargo Canc Ctr, BR-01508010 Sao Paulo, SP - Brazil
[5] Inst Canc Res, London SW7 3RP - England
[6] Univ Estadual Paulista UNESP, Botucatu Med Sch, Dept Pathol, BR-18618970 Botucatu, SP - Brazil
[7] Barretos Sch Hlth Sci, Dr Paulo Prata FACISB, BR-14785002 Barretos, SP - Brazil
[8] Univ Minho, Sch Med, Life & Hlth Sci Res Inst ICVS, P-4710057 Braga - Portugal
[9] 3Bs PT Govt Associate Lab, P-4806909 Braga - Portugal
Total Affiliations: 9
Document type: Journal article
Source: CELLS; v. 9, n. 2 FEB 2020.
Web of Science Citations: 0
Abstract

The 5'-methylthioadenosine phosphorylase (MTAP) gene is located in the chromosomal region 9p21. MTAP deletion is a frequent event in a wide variety of human cancers; however, its biological role in tumorigenesis remains unclear. The purpose of this study was to characterize the MTAP expression profile in a series of gliomas and to associate it with patients' clinicopathological features. Moreover, we sought to evaluate, through glioma gene-edited cell lines, the biological impact of MTAP in gliomas. MTAP expression was evaluated in 507 glioma patients by immunohistochemistry (IHC), and the expression levels were associated with patients' clinicopathological features. Furthermore, an in silico study was undertaken using genomic databases totalizing 350 samples. In glioma cell lines, MTAP was edited, and following MTAP overexpression and knockout (KO), a transcriptome analysis was performed by NanoString Pan-Cancer Pathways panel. Moreover, MTAP's role in glioma cell proliferation, migration, and invasion was evaluated. Homozygous deletion of 9p21 locus was associated with a reduction of MTAP mRNA expression in the TCGA (The Cancer Genome Atlas) - glioblastoma dataset (p < 0.01). In addition, the loss of MTAP expression was markedly high in high-grade gliomas (46.6% of cases) determined by IHC and Western blotting (40% of evaluated cell lines). Reduced MTAP expression was associated with a better prognostic in the adult glioblastoma dataset (p < 0.001). Nine genes associated with five pathways were differentially expressed in MTAP-knockout (KO) cells, with six upregulated and three downregulated in MTAP. Analysis of cell proliferation, migration, and invasion did not show any significant differences between MTAP gene-edited and control cells. Our results integrating data from patients as well as in silico and in vitro models provide evidence towards the lack of strong biological importance of MTAP in gliomas. Despite the frequent loss of MTAP, it seems not to have a clinical impact in survival and does not act as a canonic tumor suppressor gene in gliomas. (AU)

FAPESP's process: 16/18907-0 - Characterization of the involvement of WNK2 protein in autophagic and endocytic vesicle traffic in glioma
Grantee:Ana Laura Vieira Alves
Support type: Scholarships in Brazil - Master
FAPESP's process: 17/22305-9 - Study of biomarkers of cetuximab response and prespective of application of anti-EGFR combi-molecules in solid tumors
Grantee:Izabela Natalia Faria Gomes
Support type: Scholarships in Brazil - Doctorate
FAPESP's process: 16/06833-2 - Molecular characterization of MTAP (Methylthioadenosine phosphorylase) and evaluation of therapeutic potential in gliomas
Grantee:Weder Pereira de Menezes
Support type: Scholarships in Brazil - Doctorate