Heat Shock Proteins in Glioblastoma Biology: Where... - BV FAPESP
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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Heat Shock Proteins in Glioblastoma Biology: Where Do We Stand?

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Author(s):
Iglesia, Rebeca Piatniczka [1] ; de Lima Fernandes, Camila Felix [1] ; Coelho, Barbara Paranhos [1] ; Prado, Mariana Brandao [1] ; Melo Escobar, Maria Isabel [1] ; Dona Rodrigues Almeida, Gustavo Henrique [1] ; Lopes, Marilene Hohmuth [1]
Total Authors: 7
Affiliation:
[1] Univ Sao Paulo, Inst Biomed Sci, Dept Cell & Dev Biol, BR-05508000 Sao Paulo, SP - Brazil
Total Affiliations: 1
Document type: Review article
Source: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; v. 20, n. 22 NOV 2019.
Web of Science Citations: 0
Abstract

Heat shock proteins (HSPs) are evolutionary conserved proteins that work as molecular chaperones and perform broad and crucial roles in proteostasis, an important process to preserve the integrity of proteins in different cell types, in health and disease. Their function in cancer is an important aspect to be considered for a better understanding of disease development and progression. Glioblastoma (GBM) is the most frequent and lethal brain cancer, with no effective therapies. In recent years, HSPs have been considered as possible targets for GBM therapy due their importance in different mechanisms that govern GBM malignance. In this review, we address current evidence on the role of several HSPs in the biology of GBMs, and how these molecules have been considered in different treatments in the context of this disease, including their activities in glioblastoma stem-like cells (GSCs), a small subpopulation able to drive GBM growth. Additionally, we highlight recent works that approach other classes of chaperones, such as histone and mitochondrial chaperones, as important molecules for GBM aggressiveness. Herein, we provide new insights into how HSPs and their partners play pivotal roles in GBM biology and may open new therapeutic avenues for GBM based on proteostasis machinery. (AU)

FAPESP's process: 18/15557-4 - Prion protein and its partners: emerging targets for glioblastoma stem cell based-therapy
Grantee:Marilene Hohmuth Lopes
Support Opportunities: Research Grants - Young Investigators Grants - Phase 2
FAPESP's process: 17/26158-0 - Prion protein as stem regulator in glioblastoma stem cells: its role in the formation and function of multiprotein signaling platforms
Grantee:Mariana Brandão Prado
Support Opportunities: Scholarships in Brazil - Doctorate (Direct)
FAPESP's process: 18/19320-9 - Gene profiling of embryonic stem cells haploinsufficient for STI1 in the maintenance of pluripotent status
Grantee:Camila Felix de Lima Fernandes
Support Opportunities: Scholarships in Brazil - Master
FAPESP's process: 19/14952-0 - Characterization of intracellular signaling pathways modulated by the cellular prion protein on stemness maintenance in glioblastoma stem cells
Grantee:Bárbara Paranhos Coelho
Support Opportunities: Scholarships in Brazil - Post-Doctoral
FAPESP's process: 17/20271-0 - Role of prion protein in the dynamic of multiprotein signaling modules related to stemness of glioblastoma stem cells: its functional role and potential therapeutic target
Grantee:Marilene Hohmuth Lopes
Support Opportunities: Regular Research Grants
FAPESP's process: 19/12710-9 - Role of cellular prion protein in temozolomide resistance: emphasis on processes modulated by hypoxia
Grantee:Rebeca Piatniczka Iglesia
Support Opportunities: Scholarships in Brazil - Post-Doctoral
FAPESP's process: 19/11097-1 - Modulation of the neural phenotype of glioblastoma stem cells by extracellular miRNA from NSCs
Grantee:Maria Isabel Melo Escobar
Support Opportunities: Scholarships in Brazil - Master