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Pre-receptor regulation of 11-oxyandrogens differs between normal and cancerous endometrium and across endometrial cancer grades and molecular subtypes
ID
Gjorgoska, Marija
(
Avtor
),
ID
Šturm, Lea
(
Avtor
),
ID
Lanišnik-Rižner, Tea
(
Avtor
)
PDF - Predstavitvena datoteka,
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MD5: 45F269043B7B347DB5877DB367141848
URL - Izvorni URL, za dostop obiščite
https://www.frontiersin.org/journals/endocrinology/articles/10.3389/fendo.2024.1404804/full
Galerija slik
Izvleček
Background: Endometrial cancer (EC) is a prevalent gynecological malignancy globally, with a rising incidence trend. While classic androgens have been implicated with EC risk, the role of their 11-oxygenated metabolites is poorly understood. Here, we studied 11-oxyandrogen formation from steroid precursors in EC for the first time. Methods: We performed in vitro studies on a panel of four EC cell lines of varying differentiation degree and molecular subtype and a control cell line of normal endometrium to assess 11-oxyandrogen formation from steroid precursors. We also characterized the transcriptomic effects of dihydrotestosterone (DHT) and 11-keto-DHT on Ishikawa and RL95-2. Key molecular players in 11-oxyandrogen metabolism and action were explored in endometrial tumors using public transcriptomic datasets. Results: We discovered that within endometrial tumors, the formation of 11-oxyandrogens does not occur from classic androgen precursors. However, we observed distinct regulatory mechanisms at a pre-receptor level in normal endometrium compared to cancerous tissue, and between low- and high-grade tumors. Specifically, in vitro models of low-grade EC formed higher levels of bioactive 11-keto-testosterone from 11-oxyandrogen precursors compared to models of noncancerous endometrium and high-grade, TP53-mutated EC. Moreover, the potent androgen, DHT and its 11-keto homologue induced mild transcriptomic effects on androgen receptor (AR)-expressing EC model, Ishikawa. Finally, using public transcriptomic datasets, we found HSD11B2 and SRD5A2, coding for key enzymes in steroid metabolism, to be associated with better disease-specific survival, whereas higher intra-tumoral AR expression correlated with lower recurrence in TP53-wt tumors. Conclusions: The intra-tumoral metabolism of 11-oxyandrogen precursors is characteristic for low-grade EC of non-TP53-alt molecular subtypes. Our findings support further exploration of circulating 11-oxyandrogens as prognostic biomarkers in EC.
Jezik:
Angleški jezik
Ključne besede:
endometrial cancer
,
11-oxyandrogens
,
intracrinology
,
androgen receptor
,
LC-MS/MS profiling
,
in vitro models
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
MF - Medicinska fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2024
Št. strani:
12 str.
Številčenje:
Vol. 15, art. 1404804
PID:
20.500.12556/RUL-166840
UDK:
616-006:577.2
ISSN pri članku:
1664-2392
DOI:
10.3389/fendo.2024.1404804
COBISS.SI-ID:
203016707
Datum objave v RUL:
27.01.2025
Število ogledov:
415
Število prenosov:
158
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Objavi na:
Gradivo je del revije
Naslov:
Frontiers in endocrinology
Založnik:
Frontiers Research Foundation
ISSN:
1664-2392
COBISS.SI-ID:
3340154
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.
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
endometrijske novotvorbe
,
11-oksiandrogeni
,
intrakrinologija
,
androgeni receptor
,
LC-MS/MS profiliranje
Projekti
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
J3-2535
Naslov:
Vloga androgenov pri hormonsko odvisnih boleznih: pomen za diagnostiko in zdravljenje
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
P3-0449
Naslov:
Translacijska molekularna endokrinologija za zdravje žensk
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