» Articles » PMID: 32153500

Experimental Evidence and Clinical Implications of Pituitary Adenoma Stem Cells

Overview
Specialty Endocrinology
Date 2020 Mar 11
PMID 32153500
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

Pituitary adenomas, accounting for 15% of diagnosed intracranial neoplasms, are usually benign and pharmacologically and surgically treatable; however, the critical location, mass effects and hormone hypersecretion sustain their significant morbidity. Approximately 35% of pituitary tumors show a less benign course since they are highly proliferative and invasive, poorly resectable, and likely recurring. The latest WHO classification of pituitary tumors includes pituitary transcription factor assessment to determine adenohypophysis cell lineages and accurate designation of adenomas, nevertheless little is known about molecular and cellular pathways which contribute to pituitary tumorigenesis. In malignant tumors the identification of cancer stem cells radically changed the concepts of both tumorigenesis and pharmacological approaches. Cancer stem cells are defined as a subset of undifferentiated transformed cells from which the bulk of cancer cells populating a tumor mass is generated. These cells are able to self-renew, promoting tumor progression and recurrence of malignant tumors, also conferring cytotoxic drug resistance. On the other hand, the existence of stem cells within benign tumors is still debated. The presence of adult stem cells in human and murine pituitaries where they sustain the high plasticity of hormone-producing cells, allowed the hypothesis that putative tumor stem cells might exist in pituitary adenomas, reinforcing the concept that the cancer stem cell model could also be applied to pituitary tumorigenesis. In the last few years, the isolation and phenotypic characterization of putative pituitary adenoma stem-like cells was performed using a wide and heterogeneous variety of experimental models and techniques, although the role of these cells in adenoma initiation and progression is still not completely definite. The assessment of possible pituitary adenoma-initiating cell population would be of extreme relevance to better understand pituitary tumor biology and to identify novel potential diagnostic markers and pharmacological targets. In this review, we summarize the most updated studies focused on the definition of pituitary adenoma stem cell phenotype and functional features, highlighting the biological processes and intracellular pathways potentially involved in driving tumor growth, relapse, and therapy resistance.

Citing Articles

Clinical features of pituitary carcinoma: analysis based on a case report and literature review.

Yang Y, Liang W, Fan K, Yang T, Cheng J Front Endocrinol (Lausanne). 2024; 15:1440247.

PMID: 39544231 PMC: 11560426. DOI: 10.3389/fendo.2024.1440247.


Comprehensive transcriptomic analysis identifies three distinct subtypes of pituitary adenomas: insights into tumor behavior, prognosis, and stem cell characteristics.

Peng J, Yuan L, Kang P, Jin S, Ma S, Zhou W J Transl Med. 2024; 22(1):892.

PMID: 39363281 PMC: 11448088. DOI: 10.1186/s12967-024-05702-w.


Exploring the Role of the TAS2R16 Protein and Its Single Nucleotide Variants in Pituitary Adenoma Development.

Pileckaite E, Vilkeviciute A, Gedvilaite-Vaicechauskiene G, Kriauciuniene L, Liutkeviciene R Biomedicines. 2024; 12(9).

PMID: 39335536 PMC: 11429365. DOI: 10.3390/biomedicines12092022.


The reporting quality of randomized controlled trials in pharmacotherapy for pituitary adenomas.

Yan H, Wang D, Zhao Y, Miao J, Wang Z Medicine (Baltimore). 2024; 103(11):e37518.

PMID: 38489678 PMC: 10939664. DOI: 10.1097/MD.0000000000037518.


Pathogenesis, clinical features, and treatment of plurihormonal pituitary adenoma.

Cai Y, Liu S, Zhao X, Ren L, Liu X, Gang X Front Neurosci. 2024; 17:1323883.

PMID: 38260014 PMC: 10800528. DOI: 10.3389/fnins.2023.1323883.


References
1.
Gremeaux L, Fu Q, Chen J, Vankelecom H . Activated phenotype of the pituitary stem/progenitor cell compartment during the early-postnatal maturation phase of the gland. Stem Cells Dev. 2011; 21(5):801-13. DOI: 10.1089/scd.2011.0496. View

2.
Liou G . CD133 as a regulator of cancer metastasis through the cancer stem cells. Int J Biochem Cell Biol. 2018; 106:1-7. PMC: 6309463. DOI: 10.1016/j.biocel.2018.10.013. View

3.
Manoranjan B, Mahendram S, Almenawer S, Venugopal C, McFarlane N, Hallett R . The identification of human pituitary adenoma-initiating cells. Acta Neuropathol Commun. 2016; 4(1):125. PMC: 5127041. DOI: 10.1186/s40478-016-0394-4. View

4.
Barbieri F, Thellung S, Wurth R, Gatto F, Corsaro A, Villa V . Emerging Targets in Pituitary Adenomas: Role of the CXCL12/CXCR4-R7 System. Int J Endocrinol. 2014; 2014:753524. PMC: 4248486. DOI: 10.1155/2014/753524. View

5.
Evans C, Moreno C, Zhan X, McCabe M, Vertino P, Desiderio D . Molecular pathogenesis of human prolactinomas identified by gene expression profiling, RT-qPCR, and proteomic analyses. Pituitary. 2008; 11(3):231-45. DOI: 10.1007/s11102-007-0082-2. View