Development of Human Pituitary Neuroendocrine Tumor Organoids to Facilitate Effective Targeted Treatments of Cushing's Disease.
Jayati ChakrabartiRitu PandeyJared M ChurkoJennifer EschbacherSaptarshi MallickYuliang ChenBeth HermesPalash MallickBen N StansfieldKelvin W PondCurtis A ThorneKevin C J YuenAndrew S LittleYana ZavrosPublished in: Cells (2022)
(1) Background: Cushing's disease (CD) is a serious endocrine disorder caused by an adrenocorticotropic hormone (ACTH)-secreting pituitary neuroendocrine tumor (PitNET) that stimulates the adrenal glands to overproduce cortisol. Chronic exposure to excess cortisol has detrimental effects on health, including increased stroke rates, diabetes, obesity, cognitive impairment, anxiety, depression, and death. The first-line treatment for CD is pituitary surgery. Current surgical remission rates reported in only 56% of patients depending on several criteria. The lack of specificity, poor tolerability, and low efficacy of the subsequent second-line medical therapies make CD a medical therapeutic challenge. One major limitation that hinders the development of specific medical therapies is the lack of relevant human model systems that recapitulate the cellular composition of PitNET microenvironment. (2) Methods: human pituitary tumor tissue was harvested during transsphenoidal surgery from CD patients to generate organoids (hPITOs). (3) Results: hPITOs generated from corticotroph, lactotroph, gonadotroph, and somatotroph tumors exhibited morphological diversity among the organoid lines between individual patients and amongst subtypes. The similarity in cell lineages between the organoid line and the patient's tumor was validated by comparing the neuropathology report to the expression pattern of PitNET specific markers, using spectral flow cytometry and exome sequencing. A high-throughput drug screen demonstrated patient-specific drug responses of hPITOs amongst each tumor subtype. Generation of induced pluripotent stem cells (iPSCs) from a CD patient carrying germline mutation CDH23 exhibited dysregulated cell lineage commitment. (4) Conclusions: The human pituitary neuroendocrine tumor organoids represent a novel approach in how we model complex pathologies in CD patients, which will enable effective personalized medicine for these patients.
Keyphrases
- end stage renal disease
- induced pluripotent stem cells
- ejection fraction
- newly diagnosed
- chronic kidney disease
- endothelial cells
- high throughput
- type diabetes
- prognostic factors
- cognitive impairment
- emergency department
- case report
- magnetic resonance
- public health
- gene expression
- adipose tissue
- clinical trial
- randomized controlled trial
- acute coronary syndrome
- body mass index
- dna methylation
- weight loss
- rheumatoid arthritis
- skeletal muscle
- brain injury
- dna repair
- systemic lupus erythematosus
- coronary artery disease
- dna damage
- human health
- study protocol
- poor prognosis
- bone marrow
- growth hormone
- genome wide
- glycemic control
- patient reported
- subarachnoid hemorrhage