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正常和肢端肥大症生长激素细胞中的生长抑素受体:临床医生对免疫组织化学报告的看法的转变——综述。

Somatostatin receptors in normal and acromegalic somatotroph cells: the U-turn of the clinician to immunohistochemistry report - a review.

机构信息

Department of Endocrinology, Carol Davila University of Medicine and Pharmacy, C. I. Parhon National Institute of Endocrinology, Bucharest, Romania;

出版信息

Rom J Morphol Embryol. 2020 Apr-Jun;61(2):353-359. doi: 10.47162/RJME.61.2.05.

DOI:10.47162/RJME.61.2.05
PMID:33544787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7864306/
Abstract

This is a narrative review of literature introducing somatostatin receptors (SSTRs) as part of understanding the somatotroph cells since they are positive in normal cells but also in tumoral cells as seen in somatotropinoma, a growth hormone (GH)-producing neoplasia, which causes acromegaly. They are five subtypes of SSTRs (1 to 5), which are immunohistochemically positive in different proportions in somatotropinomas. SSTR types 2 and 5 are most frequent in GH-secreting adenomas and they are both targeted by medical therapy with somatostatin analogues (SSTAs) like first generation Octreotide and Lanreotide (mainly targeting SSTR2) and second generation Pasireotide (with highest affinity for SSTR5), thus heterogeneous SSTRs configuration into the tumor explains different pattern of response to treatment and it might predict it once the SSTRs immunostaining is performed. Monoclonal antibodies are used for immunohistochemical detection of SSTRs; currently, a lack of standardization is presented, and scoring systems, such as Volante, H-score or human epidermal growth factor receptor 2 (HER2)-score, are applied. Immunoreactive markers like SSTRs are the U-turn in clinical practice regarding somatotropinomas since the configuration of subtypes 2 and 5 explains the responsiveness to medical therapy like SSTA. Further achievement of disease control is imperiously necessary because acromegaly has an increased rate of morbidity and mortality.

摘要

这是一篇介绍生长抑素受体 (SSTRs) 的文献综述,旨在帮助理解生长激素细胞,因为这些受体在正常细胞和肿瘤细胞中均呈阳性,如生长激素细胞瘤,这是一种产生生长激素的肿瘤,会导致肢端肥大症。SSTR 有 5 种亚型 (1 到 5),在生长激素腺瘤中以不同比例免疫组织化学阳性。SSTR 类型 2 和 5 在分泌生长激素的腺瘤中最为常见,它们都是生长抑素类似物 (SSTAs) 治疗的靶点,如第一代奥曲肽和兰瑞肽(主要靶向 SSTR2)和第二代培高利特(对 SSTR5 的亲和力最高),因此肿瘤中不同的 SSTR 构型解释了对治疗的不同反应模式,一旦进行 SSTR 免疫染色,就可以预测这种反应。单克隆抗体用于 SSTR 的免疫组织化学检测;目前,存在缺乏标准化的问题,应用评分系统,如 Volante、H 评分或人表皮生长因子受体 2 (HER2) 评分。像 SSTR 这样的免疫反应性标志物是生长激素细胞瘤临床实践的转折点,因为亚型 2 和 5 的构型解释了对 SSTA 等药物治疗的反应性。进一步实现疾病控制是必要的,因为肢端肥大症的发病率和死亡率增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ca/7864306/d57c4dcaf95d/RJME-61-2-353-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ca/7864306/8d1e7741144a/RJME-61-2-353-fig1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ca/7864306/68c1e87e685a/RJME-61-2-353-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ca/7864306/d57c4dcaf95d/RJME-61-2-353-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ca/7864306/8d1e7741144a/RJME-61-2-353-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ca/7864306/7fcf68187541/RJME-61-2-353-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ca/7864306/ee331e595e65/RJME-61-2-353-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ca/7864306/4e84b0ea97dd/RJME-61-2-353-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ca/7864306/2a6bf62287ee/RJME-61-2-353-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ca/7864306/68c1e87e685a/RJME-61-2-353-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ca/7864306/d57c4dcaf95d/RJME-61-2-353-fig7.jpg

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