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MAPK7 variants related to prognosis and chemotherapy response in osteosarcoma.

Authors :
Tesser-Gamba F
Paolillo AT
Del Giúdice Paniago M
Petrilli AS
Seixas Alves MT
Garcia Filho RJ
Toledo SRC
Source :
Annals of diagnostic pathology [Ann Diagn Pathol] 2020 Jun; Vol. 46, pp. 151482. Date of Electronic Publication: 2020 Feb 19.
Publication Year :
2020

Abstract

Osteosarcoma (OS) is a class of cancer originating from the bone, affecting mainly children and young adults. Our previous study showed that MAPK7 gene overexpression was significantly associated with tumor progression, poor treatment response, and worse overall survival, suggesting that MAPK7 could play an important role in OS tumorigenesis. We have investigated if MAPK7 overexpression was a result of any genomic changes in OS tumor specimens. We identified five SNPs (Single Nucleotide Polymorphism) previously described in databases, dbSNP and COSMIC, and identified two single nucleotide substitution not yet described. We found, in prechemotherapy specimens, a significant association of MAPK7 rs2233072G allele variant with metastasis at diagnosis and relapse (0.0909 and 0.0455, respectively). In post-chemotherapy, rs1054206GG specimen's genotype was associated with osteoblastic histological type (P= 0.0249) and presented decreased MAPK7 gene expression when compared with pre-chemotherapy specimens of same patients (P = 0.0095). Interestingly, it was observed some SNPs genotype exchange after chemotherapy. Our data indicated that MAPK7 gene expression associated with genotype exchange after chemotherapy, and these SNPs associated with important clinical parameters might be a valuable indicator for predicting in OS.<br />Competing Interests: Declaration of competing interest The authors declare that there is no conflict of interest that could constitute an impediment to the publication of this article.<br /> (Copyright © 2020 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1532-8198
Volume :
46
Database :
MEDLINE
Journal :
Annals of diagnostic pathology
Publication Type :
Academic Journal
Accession number :
32145682
Full Text :
https://doi.org/10.1016/j.anndiagpath.2020.151482