Evidence map›Paper›PMID 36359740›Full record

ArticleCells2022

Development of Human Pituitary Neuroendocrine Tumor Organoids to Facilitate Effective Targeted Treatments of Cushing's Disease.

Jayati Chakrabarti, Ritu Pandey, Jared M Churko, Jennifer Eschbacher, Saptarshi Mallick, Yuliang Chen, Beth Hermes, Palash Mallick, Ben N Stansfield, Kelvin W Pond and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
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  4. Modeling pediatric brain tumors with human stem cells.Frontiers in cellular neuroscience · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

Jayati ChakrabartiDepartment of Cellular and Molecular Medicine, University of Arizona College of Medicine, Tucson, AZ 85721, USA.ORCID 0000-0003-2265-4657
Ritu PandeyDepartment of Cellular and Molecular Medicine, University of Arizona College of Medicine, Tucson, AZ 85721, USA.
Jared M ChurkoDepartment of Cellular and Molecular Medicine, University of Arizona College of Medicine, Tucson, AZ 85721, USA.
Jennifer EschbacherDepartment of Neuropathology, Barrow Neurological Institute, Phoenix, AZ 85013, USA.
Saptarshi MallickDepartment of Cellular and Molecular Medicine, University of Arizona College of Medicine, Tucson, AZ 85721, USA.ORCID 0000-0002-2147-3478
Yuliang ChenUniversity of Arizona Cancer Center Bioinformatics Core, Tucson, AZ 85721, USA.
Beth HermesDepartment of Neuropathology, Barrow Neurological Institute, Phoenix, AZ 85013, USA.
Palash MallickDepartment of Cellular and Molecular Medicine, University of Arizona College of Medicine, Tucson, AZ 85721, USA.
Ben N StansfieldDepartment of Cellular and Molecular Medicine, University of Arizona College of Medicine, Tucson, AZ 85721, USA.ORCID 0000-0003-2061-9428
Kelvin W PondDepartment of Cellular and Molecular Medicine, University of Arizona College of Medicine, Tucson, AZ 85721, USA.
Curtis A ThorneDepartment of Cellular and Molecular Medicine, University of Arizona College of Medicine, Tucson, AZ 85721, USA.
Kevin C J YuenDepartment of Neuroendocrinology, Barrow Neurological Institute, Phoenix, AZ 85013, USA.
Andrew S LittleDepartment of Neurosurgery, Barrow Neurological Institute, Phoenix, AZ 85013, USA.
Yana ZavrosDepartment of Cellular and Molecular Medicine, University of Arizona College of Medicine, Tucson, AZ 85721, USA.
University of Arizona · USBarrow Neurological Institute · US

Funding

VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Dan Theodorescu · 1985 to 2026
$110.2M
Defining signaling networks in epithelial homeostasisR35GM147128 · NIGMS · UNIVERSITY OF ARIZONA · PI Curtis Andrew Thorne · 2022 to 2026
$2.0M
NCI NIH HHS P30 CA023074NIGMS NIH HHS R35 GM147128
6 · The paper itself

Abstract

(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.

Indexed as

Neuroendocrine TumorsPituitary ACTH HypersecretionPituitary NeoplasmsHumansHydrocortisoneOrganoidsTumor MicroenvironmentHydrocortisoneCDH23induced pluripotent stem cellsneuroendocrine tumorsorganoids

Identifiers

PMID36359740
PMCPMC9659185
OpenAlexW4307927805

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.