Academic Journal

Differences in Immunological Landscape between EGFR-Mutated and Wild-Type Lung Adenocarcinoma

التفاصيل البيبلوغرافية
العنوان: Differences in Immunological Landscape between EGFR-Mutated and Wild-Type Lung Adenocarcinoma
المؤلفون: Jia-Wei Luo, Yan-Hua Guo, Feng-Ying Wu, Xue-Fei Li, Xue-Cheng Sun, Jia-Lu Wang, Cai-Cun Zhou
المصدر: Disease Markers, Vol 2021 (2021)
بيانات النشر: Hindawi Limited
سنة النشر: 2021
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: Medicine (General), R5-920
الوصف: Recent clinical trials of lung adenocarcinoma with immune checkpoint inhibitors revealed that lung adenocarcinoma patients with EGFR mutations have a poor response to immunotherapy. However, the mechanisms have not been addressed. We performed immunohistochemistry analyses of resected lung adenocarcinoma tissues with and without EGFR mutations to investigate and compare the characteristics of the tumor microenvironment (TME). We retrospectively enrolled a total of 323 lung adenocarcinoma patients (164 had EGFR mutations), and their corresponding tissue samples were analyzed by the EGFR mutation test and immunohistochemistry. We selected the markers of the immune checkpoint molecule (PD1, PD-L1, and LAG-3) and immune cell (CD3, CD4, CD8, and Foxp3) as markers of the tumor microenvironment. Our results revealed that patients had a distinct tumor microenvironment between EGFR-mutant and wild-type lung adenocarcinomas; the expression of CD3, CD4, PD-L1, and Foxp3 in EGFR-mutant tumors was significantly higher than that in wild-type tumors, while the expression of LAG3 and PD-1 showed a positive correlation with EGFR-wild-type tumors. In survival analysis, EGFR-wild-type patients had longer disease-free survival (DFS) than EGFR-mutant patients (P=0.0065). Our research demonstrates significant differences in tumor microenvironment composition between EGFR-mutant and wild-type patients. Our findings provide novel evidence that contributes to understanding the mechanism underlying the poor efficacy of immune checkpoint inhibitors.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 0278-0240
1875-8630
Relation: http://dx.doi.org/10.1155/2021/3776854; https://doaj.org/toc/0278-0240; https://doaj.org/toc/1875-8630; https://doaj.org/article/03b3ad6b59a94f0aa0124dcc0c61631e
DOI: 10.1155/2021/3776854
الاتاحة: https://doi.org/10.1155/2021/3776854
https://doaj.org/article/03b3ad6b59a94f0aa0124dcc0c61631e
رقم الانضمام: edsbas.4E2AEA9E
قاعدة البيانات: BASE
الوصف
تدمد:02780240
18758630
DOI:10.1155/2021/3776854