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Molecular pathways involved in the development of congenital erythrocytosis
ID
Tomc, Jana
(
Avtor
),
ID
Debeljak, Nataša
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(1,83 MB)
MD5: E172E654ADD3E49571EB2A4E93E3CBF6
URL - Izvorni URL, za dostop obiščite
https://www.mdpi.com/2073-4425/12/8/1150
Galerija slik
Izvleček
Patients with idiopathic erythrocytosis are directed to targeted genetic testing including nine genes involved in oxygen sensing pathway in kidneys, erythropoietin signal transduction in pre-erythrocytes and hemoglobin-oxygen affinity regulation in mature erythrocytes. However, in more than 60% of cases the genetic cause remains undiagnosed, suggesting that other genes and mechanisms must be involved in the disease development. This review aims to explore additional molecular mechanisms in recognized erythrocytosis pathways and propose new pathways associated with this rare hematological disorder. For this purpose, a comprehensive review of the literature was performed and different in silico tools were used. We identified genes involved in several mechanisms and molecular pathways, including mRNA transcriptional regulation, post-translational modifications, membrane transport, regulation of signal transduction, glucose metabolism and iron homeostasis, which have the potential to influence the main erythrocytosis-associated pathways. We provide valuable theoretical information for deeper insight into possible mechanisms of disease development. This information can be also helpful to improve the current diagnostic solutions for patients with idiopathic erythrocytosis.
Jezik:
Angleški jezik
Ključne besede:
erythrocytosis
,
disease mechanisms
,
metabolomics
,
congenital
,
familial
,
signal transduction
,
transcriptomic
,
proteomic
Vrsta gradiva:
Članek v reviji
Tipologija:
1.02 - Pregledni znanstveni članek
Organizacija:
MF - Medicinska fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2021
Št. strani:
20 str.
Številčenje:
Vol. 12, iss. 8, art. 1150
PID:
20.500.12556/RUL-135705
UDK:
616.1
ISSN pri članku:
2073-4425
DOI:
10.3390/genes12081150
COBISS.SI-ID:
72028419
Datum objave v RUL:
29.03.2022
Število ogledov:
722
Število prenosov:
110
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
Genes
Skrajšan naslov:
Genes
Založnik:
Multidisciplinary Digital Publishing Institute (MDPI)
ISSN:
2073-4425
COBISS.SI-ID:
523100185
Licence
Licenca:
CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:
To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Začetek licenciranja:
01.08.2021
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
eritrocitoza
,
mehanizmi bolezni
,
metabolomika
Projekti
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
L3-9279
Naslov:
Genetska osnova eritrocitoz v Sloveniji
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
P1-0390
Naslov:
Funkcijska genomika in biotehnologija za zdravje
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