Section of Pharmacology, Dipartimento di Medicina Interna and Centro di Eccellenza per la Ricerca Biomedica (CEBR), Università di Genova, Genoa, Italy.
IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Front Endocrinol (Lausanne). 2020 Feb 20;11:54. doi: 10.3389/fendo.2020.00054. eCollection 2020.
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.
垂体腺瘤占颅内肿瘤的 15%,通常为良性,可通过药物和手术治疗;但由于其位置关键、占位效应和激素分泌过度,仍存在较高的发病率。约 35%的垂体瘤具有较差的生物学行为,因为它们增殖和侵袭性强、难以完全切除,且可能复发。最新的世界卫生组织垂体肿瘤分类包括对垂体转录因子的评估,以确定腺垂体细胞谱系,并准确指定腺瘤,然而,人们对导致垂体肿瘤发生的分子和细胞途径知之甚少。在恶性肿瘤中,癌症干细胞的鉴定彻底改变了肿瘤发生和药物治疗方法的概念。癌症干细胞被定义为未分化转化细胞的一个亚群,肿瘤细胞群的大部分就是由这些细胞产生的。这些细胞能够自我更新,促进肿瘤的进展和恶性肿瘤的复发,并赋予细胞毒性药物耐药性。另一方面,良性肿瘤中是否存在干细胞仍存在争议。在人类和鼠类垂体中存在成体干细胞,它们维持着产生激素细胞的高可塑性,这使得假设在垂体腺瘤中可能存在肿瘤干细胞,也强化了癌症干细胞模型也可能适用于垂体肿瘤发生的概念。在过去的几年中,使用广泛而多样的实验模型和技术,对所谓的垂体腺瘤干细胞样细胞进行了分离和表型特征分析,尽管这些细胞在腺瘤起始和进展中的作用仍不完全确定。评估潜在的垂体腺瘤起始细胞群对于更好地了解垂体肿瘤生物学以及识别新的潜在诊断标志物和药物靶点具有重要意义。在这篇综述中,我们总结了最新的研究,重点介绍了垂体腺瘤干细胞表型和功能特征的定义,强调了潜在涉及驱动肿瘤生长、复发和治疗抵抗的生物学过程和细胞内途径。