The Association of Cholesterol Uptake and Synthesis with Histology and Genotype in Cortisol-Producing Adenoma (CPA)

Authors
Motomura, NaokiYamazaki, YutoKoga, DaikiHarashima, ShogoGao, XinTezuka, YutaOmata, KeiOno, YoshikiyoMorimoto, RyoSatoh, FumitoshiNakamura, YasuhiroKwon, Go EunChoi, Man HoIto, AkihiroSasano, Hironobu
Issue Date
2022-02
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Citation
International Journal of Molecular Sciences, v.23, no.4
Abstract
Cortisol-producing adenoma (CPA) is composed of clear and compact cells. Clear cells are lipid abundant, and compact ones lipid poor but associated with higher production of steroid hormones. PRKACA mutation (PRKACA mt) in CPA patients was reported to be associated with more pronounced clinical manifestation of Cushing's syndrome. In this study, we examined the association of histological features and genotypes with cholesterol uptake receptors and synthetic enzymes in 40 CPA cases, and with the quantitative results obtained by gas chromatography-mass spectrometry (GC-MS) analysis in 33 cases to explore their biological and clinical significance. Both cholesterol uptake receptors and synthetic enzymes were more abundant in compact cells. GC-MS analysis demonstrated that the percentage of compact cells was inversely correlated with the concentrations of cholesterol and cholesterol esters, and positively with the activity of cholesterol biosynthesis from cholesterol esters. In addition, hormone-sensitive lipase (HSL), which catalyzes cholesterol biosynthesis from cholesterol esters, tended to be more abundant in compact cells of PRKACA mt CPAs. These results demonstrated that both cholesterol uptake and biosynthesis were more pronounced in compact cells in CPA. In addition, more pronounced HSL expression in compact cells of PRKACA mt CPA could contribute to their more pronounced clinical manifestation.
Keywords
HORMONE-SENSITIVE LIPASE; CATALYTIC SUBUNIT; CUSHINGS-SYNDROME; SOMATIC MUTATIONS; PRKACA MUTATIONS; RECEPTOR; LESIONS; BI; Cushing' s syndrome; cortisol producing adenoma; cholesterol uptake; de novo synthesis; HSL; PRKACA; immunohistochemistry; mass spectrometry
ISSN
1661-6596
URI
https://pubs.kist.re.kr/handle/201004/115652
DOI
10.3390/ijms23042174
Appears in Collections:
KIST Article > 2022
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