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PMID: 35301087 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

PIMREG expression level predicts glioblastoma patient survival and affects temozolomide resistance and DNA damage response.

Biochimica et biophysica acta. Molecular basis of disease ·Vol. 1868 ·No. 6 ·2022-00-01 ·页码 166382

Serafim RB, Cardoso C, Arfelli VC, Valente V, Archangelo LF

Abstract

PIMREG expression strongly correlates with cellular proliferation in both malignant and normal cells. Throughout embryo development, PIMREG expression is prominent in the central nervous system. Recent studies have described elevated PIMREG expression in different types of tumors, which correlates with patient survival and tumor aggressiveness. Given the emerging significance of PIMREG in carcinogenesis and its putative role in the context of the nervous system, we investigated the expression and function of PIMREG in gliomas, the most common primary brain tumors. We performed an extensive analysis of PIMREG expression in tumors samples from glioma patients. We then assessed the effects of PIMREG silencing and overexpression on the sensitivity of glioblastoma cell lines treated with genotoxic agents commonly used for treating patients and assessed for treatment response, proliferation and migration. Our analysis shows that glioblastoma exhibits the highest levels of PIMREG expression among all cancers analyzed and that elevated PIMREG expression is a biomarker for glioma progression and patient outcome. Moreover, PIMREG is induced by genotoxic agents, and its silencing renders glioblastoma cells sensitive to temozolomide treatment and affects ATR- and ATM-dependent signaling. Our data demonstrate that PIMREG is involved in DNA damage response and temozolomide resistance of glioblastoma cells and further supports a role for PIMREG in tumorigenesis.

Keywords
ATM ATR DNA damage response GBM Gliomas Temozolomide resistance
MeSH 主题词
Antineoplastic Agents, Alkylating/pharmacology,therapeutic use Cell Line, Tumor DNA Damage Glioblastoma/drug therapy,genetics,metabolism Humans Temozolomide/pharmacology,therapeutic use
化学物质
Antineoplastic Agents, Alkylating Temozolomide
作者与单位
共 5 位作者,点击展开单位 / ORCID
Serafim Rodolfo Bortolozo
Department of Cellular and Molecular Biology and Pathogenic Bioagents, Ribeirão Preto Medical School, University of São Paulo (FMRP-USP), Ribeirão Preto, São Paulo, Brazil; Department of Genetics, Ribeirão Preto Medical School, University of São Paulo (FMRP-USP), Ribeirão Preto, São Paulo, Brazil.
Cardoso Cibele
Department of Cellular and Molecular Biology and Pathogenic Bioagents, Ribeirão Preto Medical School, University of São Paulo (FMRP-USP), Ribeirão Preto, São Paulo, Brazil; Department of Genetics, Ribeirão Preto Medical School, University of São Paulo (FMRP-USP), Ribeirão Preto, São Paulo, Brazil.
Arfelli Vanessa Cristina
Department of Cellular and Molecular Biology and Pathogenic Bioagents, Ribeirão Preto Medical School, University of São Paulo (FMRP-USP), Ribeirão Preto, São Paulo, Brazil.
Valente Valeria
School of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo, Brazil.
Archangelo Leticia Fröhlich
Department of Cellular and Molecular Biology and Pathogenic Bioagents, Ribeirão Preto Medical School, University of São Paulo (FMRP-USP), Ribeirão Preto, São Paulo, Brazil. Electronic address: [email protected].
Article Info
Journal
Biochimica et biophysica acta. Molecular basis of disease
Abbr.
Biochim Biophys Acta Mol Basis Dis
ISSN
1879-260X
Corresponding email
Published
2022-00-01
电子出版
2022-00-14
页码
166382
Language
English
Country/Region
Netherlands
NLM ID
101731730
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