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垂体神经内分泌肿瘤的表型转化

Phenotype Transformation of PitNETs.

作者信息

Li Zhenwei, Wu Yinzi, He Guannan, Wang Renzhi, Bao Xinjie

机构信息

Department of Neurosurgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.

出版信息

Cancers (Basel). 2024 Apr 29;16(9):1731. doi: 10.3390/cancers16091731.

DOI:10.3390/cancers16091731
PMID:38730682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11083144/
Abstract

Phenotype transformation in pituitary neuroendocrine tumors is a little-known and unpredictable clinical phenomenon. Previous studies have not clearly defined and systematically concluded on the causes of this rare phenomenon. Additionally, the mechanisms of phenotype transformation are not well known. We reviewed cases reported in the literature with the aim of defining phenotype transformation in pituitary neuroendocrine tumors. We present an overview of the wide spectrum of phenotype transformation and its clinical features. We also discuss findings on the potential mechanism of this rare transformation, which may be related to PC1/3, the bioactivity of secretory hormones, gene mutations and the plasticity of pituitary neuroendocrine tumors. Clinicians should be aware of this rare phenomenon and more studies on the underlying mechanisms are required.

摘要

垂体神经内分泌肿瘤中的表型转化是一种鲜为人知且不可预测的临床现象。先前的研究尚未明确界定并系统总结这一罕见现象的成因。此外,表型转化的机制也尚不明确。我们回顾了文献中报道的病例,旨在明确垂体神经内分泌肿瘤中的表型转化。我们概述了广泛的表型转化及其临床特征。我们还讨论了关于这种罕见转化潜在机制的研究结果,其可能与PC1/3、分泌激素的生物活性、基因突变以及垂体神经内分泌肿瘤的可塑性有关。临床医生应意识到这一罕见现象,并且需要对其潜在机制进行更多研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3863/11083144/ffcfcf9d2dbf/cancers-16-01731-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3863/11083144/0cb4f86f38b2/cancers-16-01731-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3863/11083144/ffcfcf9d2dbf/cancers-16-01731-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3863/11083144/0cb4f86f38b2/cancers-16-01731-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3863/11083144/ffcfcf9d2dbf/cancers-16-01731-g002.jpg

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1
Phenotype Transformation of PitNETs.垂体神经内分泌肿瘤的表型转化
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本文引用的文献

1
Erythropoietin-producing hepatocellular receptor B6 is highly expressed in non-functioning pituitary neuroendocrine tumors and its expression correlates with tumor size.产生红细胞生成素的肝细胞受体 B6 在无功能垂体神经内分泌肿瘤中高度表达,其表达与肿瘤大小相关。
Mol Biol Rep. 2024 Feb 11;51(1):297. doi: 10.1007/s11033-023-09186-7.
2
Aggressive and Metastatic Pituitary Neuroendocrine Tumors: Therapeutic Management and Off-Label Drug Use.侵袭性和转移性垂体神经内分泌肿瘤:治疗管理与超说明书用药
J Clin Med. 2023 Dec 25;13(1):116. doi: 10.3390/jcm13010116.
3
Update on Current Evidence for the Diagnosis and Management of Nonfunctioning Pituitary Neuroendocrine Tumors.
非功能性垂体神经内分泌肿瘤的诊断和治疗的最新证据更新。
Endocrinol Metab (Seoul). 2023 Dec;38(6):631-654. doi: 10.3803/EnM.2023.1838. Epub 2023 Nov 15.
4
Discontinuation of Drug Treatment in Cushing's Disease Not Cured by Pituitary Surgery.垂体手术未治愈的库欣病患者药物治疗的停药情况
J Clin Endocrinol Metab. 2024 Mar 15;109(4):1000-1011. doi: 10.1210/clinem/dgad662.
5
Oxidative stress in pituitary neuroendocrine tumors: Affecting the tumor microenvironment and becoming a new target for pituitary neuroendocrine tumor therapy.垂体神经内分泌肿瘤中的氧化应激:影响肿瘤微环境并成为垂体神经内分泌肿瘤治疗的新靶点。
CNS Neurosci Ther. 2023 Oct;29(10):2744-2759. doi: 10.1111/cns.14315. Epub 2023 Jun 21.
6
Acromegaly complicated with fulminant pituitary apoplexy: clinical characteristic analysis and review of literature.肢端肥大症并发暴发性垂体卒中:临床特征分析及文献复习。
Endocrine. 2023 Jul;81(1):160-167. doi: 10.1007/s12020-023-03379-7. Epub 2023 May 17.
7
Case Report: Progression of a Silent Corticotroph Tumor to an Aggressive Secreting Corticotroph Tumor, Treated by Temozolomide. Changes in the Clinic, the Pathology, and the β-Catenin and α-SMA Expression.病例报告:无功能性促肾上腺皮质激素细胞瘤进展为侵袭性分泌促肾上腺皮质激素细胞瘤,并用替莫唑胺治疗。临床、病理和β-连环蛋白及α-平滑肌肌动蛋白表达的变化。
Front Endocrinol (Lausanne). 2022 Jul 19;13:870172. doi: 10.3389/fendo.2022.870172. eCollection 2022.
8
Overview of the 2022 WHO Classification of Pituitary Tumors.《2022 年世卫组织垂体肿瘤分类概述》。
Endocr Pathol. 2022 Mar;33(1):6-26. doi: 10.1007/s12022-022-09703-7. Epub 2022 Mar 15.
9
Metachronous Double Pituitary Adenoma with Altered Transcriptional Factor Profile: A Case Report and Literature Review.异时性双垂体腺瘤伴转录因子谱改变:一例报告及文献复习
NMC Case Rep J. 2021 Oct 7;8(1):657-663. doi: 10.2176/nmccrj.cr.2021-0121. eCollection 2021.
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Radiomics analysis allows for precise prediction of silent corticotroph adenoma among non-functioning pituitary adenomas.影像组学分析可精准预测无功能垂体腺瘤中的静默促肾上腺皮质激素腺瘤。
Eur Radiol. 2022 Mar;32(3):1570-1578. doi: 10.1007/s00330-021-08361-3. Epub 2021 Nov 27.