Human neurodegenerative diseases occur as a result of various factors. Regardless of the variety in the etiology of development, many of these diseases are characterized by the accumulation of pathological, misfolded proteins; hence, such diseases are considered as proteinopathies. While plenty of research study has been conducted in order to identify the pathophysiology of these proteinopathies, there is still a lack of understanding in terms of potential therapeutic targets. Molecular chaperones present the main workforce for cellular protection and stress response. Therefore, considering these functions, molecular chaperones present a promising target for research within the field of conformational diseases that arise from proteinopathies. Since the association between neurodegenerative disorders and their long-term consequences is well documented, the need for the development of new therapeutic strategies becomes even more critical. In this review, we summarized the molecular function of heat shock proteins and recent progress on their role, involvement, and other mechanisms related to neurodegeneration caused by different etiological factors. Based on the relevant scientific data, we will highlight the functional classification of heat shock proteins, regulatin, and their therapeutic potential for neurodegenerative disorders.

Impact of Heat Shock Proteins in Neurodegeneration: Possible Therapeutical Targets / G. Beretta, A.L. Shala. - In: ANNALS OF NEUROSCIENCES. - ISSN 0972-7531. - 29:1(2022 Jan), pp. 097275312110705.71-097275312110705.82. [10.1177/09727531211070528]

Impact of Heat Shock Proteins in Neurodegeneration: Possible Therapeutical Targets

G. Beretta
Primo
Writing – Original Draft Preparation
;
2022

Abstract

Human neurodegenerative diseases occur as a result of various factors. Regardless of the variety in the etiology of development, many of these diseases are characterized by the accumulation of pathological, misfolded proteins; hence, such diseases are considered as proteinopathies. While plenty of research study has been conducted in order to identify the pathophysiology of these proteinopathies, there is still a lack of understanding in terms of potential therapeutic targets. Molecular chaperones present the main workforce for cellular protection and stress response. Therefore, considering these functions, molecular chaperones present a promising target for research within the field of conformational diseases that arise from proteinopathies. Since the association between neurodegenerative disorders and their long-term consequences is well documented, the need for the development of new therapeutic strategies becomes even more critical. In this review, we summarized the molecular function of heat shock proteins and recent progress on their role, involvement, and other mechanisms related to neurodegeneration caused by different etiological factors. Based on the relevant scientific data, we will highlight the functional classification of heat shock proteins, regulatin, and their therapeutic potential for neurodegenerative disorders.
English
Alzheimer disease; Guillain–Barré syndrome; Heat shock protein; HSP27; HSP70; HSP90; Neurodegeneration; Parkinson disease;
Settore CHIM/08 - Chimica Farmaceutica
Review essay
Esperti anonimi
Ricerca di base
Pubblicazione scientifica
gen-2022
SAGE Publications
29
1
097275312110705
71
82
12
Pubblicato
Periodico con rilevanza internazionale
https://journals.sagepub.com/doi/10.1177/09727531211070528
scopus
crossref
datacite
Aderisco
info:eu-repo/semantics/article
Impact of Heat Shock Proteins in Neurodegeneration: Possible Therapeutical Targets / G. Beretta, A.L. Shala. - In: ANNALS OF NEUROSCIENCES. - ISSN 0972-7531. - 29:1(2022 Jan), pp. 097275312110705.71-097275312110705.82. [10.1177/09727531211070528]
open
Prodotti della ricerca::01 - Articolo su periodico
2
262
Article (author)
no
G. Beretta, A.L. Shala
File in questo prodotto:
File Dimensione Formato  
09727531211070528.pdf

accesso aperto

Tipologia: Publisher's version/PDF
Dimensione 940.89 kB
Formato Adobe PDF
940.89 kB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/922396
Citazioni
  • ???jsp.display-item.citation.pmc??? 24
  • Scopus 33
  • ???jsp.display-item.citation.isi??? 29
  • OpenAlex ND
social impact