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免疫组织化学和实时聚合酶链反应方法检测恶性胸膜间皮瘤中 pd-l1(cd274)、pd-l2(pdcd1lg2) 和 ctla-4 的表达。

Investigation of pd-l1 (cd274), pd-l2 (pdcd1lg2), and ctla-4 expressions in malignant pleural mesothelioma by immunohistochemistry and real-time polymerase chain reaction methods.

机构信息

Department of Pathology, University of Health Sciences Gazi Yasargil Trainning and Research Hospital, Diyarbakir, Turkey.

Pathology Department, Medical School, Dicle University, Diyarbakir, Turkey.

出版信息

Pol J Pathol. 2022;73(2):111-119. doi: 10.5114/pjp.2022.119752.


DOI:10.5114/pjp.2022.119752
PMID:36172747
Abstract

INTRODUCTION: Malignant pleural mesothelioma (MPM) is an aggressive malignant disease with a poor prognosis, which affects the surface mesothelium of the pleural cavity. Immune checkpoints are responsible for controlling the immune system to avoid autoimmunity and prevent tissue damage. In this study, we aimed to investigate the expression of cytotoxic T lymphocyte antigen-4 (CTLA-4), programmed death ligand 1 (PD-L1), and programmed death ligand 2 (PD-L2) immuno-control receptors in MPM patients and the relationship of the expression with tumour types and prognostic parameters. MATERIAL AND METHODS: In this study, we evaluated 50 MPM cases. Immunohistochemically CTLA-4, PD-L1, and PD-L2 were detected by using monoclonal anti-CTLA-4, anti-PD-L1, and anti-PD-L2. Real-time polymerase chain reaction (RT-PCR) analysis was performed with the primers CTLA-4, PD-L1, and PD-L2. RESULTS: Statistically, no significant relation was determined between the PD-L1, PD-L2, and CTLA-4 expressions (immunohistochemical and RT-PCR methods) and the MPM histological type. Interestingly significant correlation was observed between the mean survival time and immunohistochemical PD-L2 expression; thus, long-term survival was observed in cases with PD-L2 expression. CONCLUSIONS: Programmed death ligand 1, PD-L2, and CTLA-4 expression were observed in some MPM cases, suggesting that treatments targeting immune checkpoints may be effective. Because immunohistochemical expression of PD-L2 is associated with better prognosis, it may provide useful clues in the follow-up of patients.

摘要

简介:恶性胸膜间皮瘤(MPM)是一种预后不良的侵袭性恶性疾病,影响胸膜腔表面间皮。免疫检查点负责控制免疫系统,以避免自身免疫并防止组织损伤。在这项研究中,我们旨在研究细胞毒性 T 淋巴细胞抗原 4(CTLA-4)、程序性死亡配体 1(PD-L1)和程序性死亡配体 2(PD-L2)免疫控制受体在 MPM 患者中的表达,以及其表达与肿瘤类型和预后参数的关系。

材料和方法:在这项研究中,我们评估了 50 例 MPM 病例。使用单克隆抗 CTLA-4、抗 PD-L1 和抗 PD-L2 进行免疫组织化学检测 CTLA-4、PD-L1 和 PD-L2。使用 CTLA-4、PD-L1 和 PD-L2 的引物进行实时聚合酶链反应(RT-PCR)分析。

结果:统计分析表明,PD-L1、PD-L2 和 CTLA-4 的表达(免疫组织化学和 RT-PCR 方法)与 MPM 组织学类型之间无显著关系。有趣的是,观察到平均生存时间与免疫组化 PD-L2 表达之间存在显著相关性;因此,PD-L2 表达的病例观察到长期生存。

结论:在一些 MPM 病例中观察到程序性死亡配体 1、PD-L2 和 CTLA-4 的表达,表明针对免疫检查点的治疗可能有效。由于 PD-L2 的免疫组织化学表达与较好的预后相关,它可能为患者的随访提供有用的线索。

相似文献

[1]
Investigation of pd-l1 (cd274), pd-l2 (pdcd1lg2), and ctla-4 expressions in malignant pleural mesothelioma by immunohistochemistry and real-time polymerase chain reaction methods.

Pol J Pathol. 2022

[2]
Programmed cell death 1 ligand 1 (PD-L1) expression is associated with poor prognosis of malignant pleural mesothelioma patients with good performance status.

Pathology. 2021-6

[3]
Tumor Suppressor microRNAs Contribute to the Regulation of PD-L1 Expression in Malignant Pleural Mesothelioma.

J Thorac Oncol. 2017-6-16

[4]
Analysis of expression of PTEN/PI3K pathway and programmed cell death ligand 1 (PD-L1) in malignant pleural mesothelioma (MPM).

Lung Cancer. 2016-6

[5]
Shorter Survival in Malignant Pleural Mesothelioma Patients With High PD-L1 Expression Associated With Sarcomatoid or Biphasic Histology Subtype: A Series of 214 Cases From the Bio-MAPS Cohort.

Clin Lung Cancer. 2019-5-13

[6]
Analysis of expression of programmed cell death 1 ligand 1 (PD-L1) in malignant pleural mesothelioma (MPM).

PLoS One. 2015-3-16

[7]
Malignant pleural mesothelioma immune microenvironment and checkpoint expression: correlation with clinical-pathological features and intratumor heterogeneity over time.

Ann Oncol. 2018-5-1

[8]
Tumour infiltrating lymphocytes and PD-L1 expression as potential predictors of outcome in patients with malignant pleural mesothelioma.

Mol Biol Rep. 2019-3-6

[9]
Expression of ALCAM (CD166) and PD-L1 (CD274) independently predicts shorter survival in malignant pleural mesothelioma.

Hum Pathol. 2017-8-12

[10]
PD-L1 expression associated with worse survival outcome in malignant pleural mesothelioma.

Asia Pac J Clin Oncol. 2018-2

引用本文的文献

[1]
Molecular Insights into Pleural Mesothelioma: Unveiling Pathogenic Mechanisms and Therapeutic Opportunities.

Diagnostics (Basel). 2025-5-24

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