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DRG2作为一种生物标志物可增强PD-L1免疫组织化学检测的预测效能。

DRG2 as a Biomarker to Enhance the Predictive Efficacy of PD-L1 Immunohistochemistry Assays.

作者信息

Mani Muralidharan, Choi Seong Hee, Kwon Hyuk Nam, Park Jeong Woo

机构信息

Department of Biochemistry, University of Wisconsin-Madison, Madison, WI 53715-1218, USA.

RopheLBio, B102, Seoul Forest M Tower, Seoul 04778, Republic of Korea.

出版信息

Biomedicines. 2024 Dec 29;13(1):56. doi: 10.3390/biomedicines13010056.

Abstract

PD-L1 immunohistochemistry (IHC) assays are used as a companion diagnostic for immunotherapy with immune checkpoint inhibitors (ICIs). However, despite the association between PD-L1 expression and clinical benefit from ICIs, the PD-L1 IHC assay is not sufficiently accurate in predicting response to ICIs; some patients with high PD-L1 expression do not respond to ICIs. Recently, researchers provided insights into why some patients with high PD-L1 expression fail to respond to ICIs. They discovered that DRG2 is a critical regulator of PD-L1 endosomal trafficking in cancer cells, which is essential for the proper localization of PD-L1 on the cell surface. Although DRG2-depleted cells express high levels of PD-L1 and are PD-L1 IHC-positive, the PD-L1 sequestered in early endosomes does not respond to ICIs. Therefore, a companion diagnostic combining DRG2 expression with a PD-L1 IHC assay may improve the therapeutic response to PD-1/PD-L1 ICIs.

摘要

程序性死亡配体1(PD-L1)免疫组化(IHC)检测被用作免疫检查点抑制剂(ICI)免疫治疗的伴随诊断方法。然而,尽管PD-L1表达与ICI临床获益之间存在关联,但PD-L1 IHC检测在预测ICI反应方面并不足够准确;一些PD-L1高表达患者对ICI无反应。最近,研究人员深入探究了为何一些PD-L1高表达患者对ICI无反应。他们发现,DRG2是癌细胞中PD-L1内体运输的关键调节因子,这对于PD-L1在细胞表面的正确定位至关重要。尽管DRG2缺失的细胞表达高水平的PD-L1且PD-L1 IHC检测呈阳性,但早期内体中隔离的PD-L1对ICI无反应。因此,将DRG2表达与PD-L1 IHC检测相结合的伴随诊断方法可能会改善对PD-1/PD-L1 ICI的治疗反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bce2/11762180/78ba26404be2/biomedicines-13-00056-g001.jpg

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