The polymorphic insertion of the luteinizing hormone receptor "insLQ" show a negative association to LHR gene expression and to the follicular fluid hormonal profile in human small antral follicles
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F18%3A10375387" target="_blank" >RIV/00216208:11130/18:10375387 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00064203:_____/18:10375387
Výsledek na webu
<a href="https://doi.org/10.1016/j.mce.2017.07.002" target="_blank" >https://doi.org/10.1016/j.mce.2017.07.002</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.mce.2017.07.002" target="_blank" >10.1016/j.mce.2017.07.002</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
The polymorphic insertion of the luteinizing hormone receptor "insLQ" show a negative association to LHR gene expression and to the follicular fluid hormonal profile in human small antral follicles
Popis výsledku v původním jazyce
The luteinizing hormone receptor (LHCGR) has a little studied polymorphic 6 bp insertion (rs4539842/insLQ). This study has evaluated the insLQ polymorphism in relation to potential associations with hormonal characteristics of human small antral follicles (hSAFs). In total, 310 hSAFs were collected from 86 women undergoing fertility preservation. Analysis included hormonal profile of 297 follicular fluid (FF) samples and 148 corresponding granulosa cells samples were evaluated by cPCR for selected genes. Significantly reduced and non-detectable mRNA levels of anti-Mullerian hormone receptor II (AMHR2) and LHCGR, respectively, were observed for insLQ]insLQ compared to -/insLQ and the -/- genotypes. Moreover, LHCGR and CYP19a1 together with oestradiol and inhibin-B were significantly increased in -/insLQ compared to the -/- genotype. The homozygous insLQ genotype showed strong significant associations to GC specific genes LHCGR and CYP19a1, which may translate into significant changes in FF hormone profiles and an altered LH signaling.
Název v anglickém jazyce
The polymorphic insertion of the luteinizing hormone receptor "insLQ" show a negative association to LHR gene expression and to the follicular fluid hormonal profile in human small antral follicles
Popis výsledku anglicky
The luteinizing hormone receptor (LHCGR) has a little studied polymorphic 6 bp insertion (rs4539842/insLQ). This study has evaluated the insLQ polymorphism in relation to potential associations with hormonal characteristics of human small antral follicles (hSAFs). In total, 310 hSAFs were collected from 86 women undergoing fertility preservation. Analysis included hormonal profile of 297 follicular fluid (FF) samples and 148 corresponding granulosa cells samples were evaluated by cPCR for selected genes. Significantly reduced and non-detectable mRNA levels of anti-Mullerian hormone receptor II (AMHR2) and LHCGR, respectively, were observed for insLQ]insLQ compared to -/insLQ and the -/- genotypes. Moreover, LHCGR and CYP19a1 together with oestradiol and inhibin-B were significantly increased in -/insLQ compared to the -/- genotype. The homozygous insLQ genotype showed strong significant associations to GC specific genes LHCGR and CYP19a1, which may translate into significant changes in FF hormone profiles and an altered LH signaling.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10600 - Biological sciences
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2018
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Molecular and Cellular Endocrinology
ISSN
0303-7207
e-ISSN
—
Svazek periodika
460
Číslo periodika v rámci svazku
15
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
6
Strana od-do
57-62
Kód UT WoS článku
000423893300006
EID výsledku v databázi Scopus
2-s2.0-85024474722