The Role of VHL in the Development of von Hippel-Lindau Disease and Erythrocytosis
Von Hippel-Lindau disease (VHL disease or VHL syndrome) is a familial multisystem neoplastic syndrome stemming from germline disease-associated variants of the VHL tumor suppressor gene on chromosome 3. VHL is involved, through the EPO-VHL-HIF signaling axis, in oxygen sensing and adaptive response to hypoxia, as well as in numerous HIF-independent pathways. The diverse roles of VHL confirm its implication in several crucial cellular processes. VHL variations have been associated with the development of VHL disease and erythrocytosis. The association between genotypes and phenotypes still remains ambiguous for the majority of mutations. It appears that there is a distinction between erythrocytosis-causing VHL variations and VHL variations causing VHL disease with tumor development. Understanding the pathogenic effects of VHL variants might better predict the prognosis and optimize management of the patient.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2022 |
---|---|
Erschienen: |
2022 |
Enthalten in: |
Zur Gesamtaufnahme - volume:13 |
---|---|
Enthalten in: |
Genes - 13(2022), 2 vom: 17. Feb. |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Hudler, Petra [VerfasserIn] |
---|
Links: |
---|
Anmerkungen: |
Date Completed 19.04.2022 Date Revised 19.04.2022 published: Electronic Citation Status MEDLINE |
---|
doi: |
10.3390/genes13020362 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM337369607 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM337369607 | ||
003 | DE-627 | ||
005 | 20231226204259.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2022 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.3390/genes13020362 |2 doi | |
028 | 5 | 2 | |a pubmed24n1124.xml |
035 | |a (DE-627)NLM337369607 | ||
035 | |a (NLM)35205407 | ||
035 | |a (PII)362 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Hudler, Petra |e verfasserin |4 aut | |
245 | 1 | 4 | |a The Role of VHL in the Development of von Hippel-Lindau Disease and Erythrocytosis |
264 | 1 | |c 2022 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 19.04.2022 | ||
500 | |a Date Revised 19.04.2022 | ||
500 | |a published: Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Von Hippel-Lindau disease (VHL disease or VHL syndrome) is a familial multisystem neoplastic syndrome stemming from germline disease-associated variants of the VHL tumor suppressor gene on chromosome 3. VHL is involved, through the EPO-VHL-HIF signaling axis, in oxygen sensing and adaptive response to hypoxia, as well as in numerous HIF-independent pathways. The diverse roles of VHL confirm its implication in several crucial cellular processes. VHL variations have been associated with the development of VHL disease and erythrocytosis. The association between genotypes and phenotypes still remains ambiguous for the majority of mutations. It appears that there is a distinction between erythrocytosis-causing VHL variations and VHL variations causing VHL disease with tumor development. Understanding the pathogenic effects of VHL variants might better predict the prognosis and optimize management of the patient | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a Review | |
650 | 4 | |a Chuvash polycythemia | |
650 | 4 | |a VHL | |
650 | 4 | |a VHL disease | |
650 | 4 | |a erythrocytosis | |
650 | 4 | |a genetic variation | |
650 | 4 | |a hemangioblastoma | |
650 | 4 | |a pheochromocytoma | |
650 | 4 | |a renal cell carcinoma | |
650 | 4 | |a retinal hemangioblastoma | |
650 | 7 | |a Von Hippel-Lindau Tumor Suppressor Protein |2 NLM | |
650 | 7 | |a EC 2.3.2.27 |2 NLM | |
650 | 7 | |a VHL protein, human |2 NLM | |
650 | 7 | |a EC 6.3.2.- |2 NLM | |
700 | 1 | |a Urbancic, Mojca |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Genes |d 2011 |g 13(2022), 2 vom: 17. Feb. |w (DE-627)NLM220446326 |x 2073-4425 |7 nnns |
773 | 1 | 8 | |g volume:13 |g year:2022 |g number:2 |g day:17 |g month:02 |
856 | 4 | 0 | |u http://dx.doi.org/10.3390/genes13020362 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 13 |j 2022 |e 2 |b 17 |c 02 |