Increased VEGF-A in solid type of lung adenocarcinoma reduces the patients' survival

被引:15
作者
Jung, Woon Yong [1 ]
Min, Kyueng-Whan [1 ]
Oh, Young Ha [1 ]
机构
[1] Hanyang Univ, Coll Med, Dept Pathol, Guri Hosp, Guri 11923, Gyeonggi Do, South Korea
关键词
WORLD-HEALTH-ORGANIZATION; DIRECTLY SUPPRESSES ACTIVATION; HISTOLOGIC SUBTYPE; GRADING SYSTEM; OVARIAN-CANCER; TUMOR-CELLS; T-CELLS; EXPRESSION; CLASSIFICATION; RECURRENCE;
D O I
10.1038/s41598-020-79907-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The histological classification of lung adenocarcinoma includes 5 types: lepidic, acinar, papillary, micropapillary and solid. The complex gene interactions and anticancer immune response of these types are not well known. The aim of this study was to reveal the survival rates, genetic alterations and immune activities of the five histological types and provide treatment strategies. This study reviewed the histological findings of 517 patients with lung adenocarcinoma from The Cancer Genome Atlas (TCGA) database and classified them into five types. We performed gene set enrichment analysis (GSEA) and survival analysis according to the different types. We found six oncogenic gene sets that were higher in lung adenocarcinoma than in normal tissues. In the survival analysis of each type, the acinar type had a favorable prognosis, and the solid subtype had an unfavorable prognosis; however, the survival differences between the other types were not significant. Our study focused on the solid type, which had the poorest prognosis. The solid type was related to adaptive immune resistance associated with elevated CD8 T cells and high CD274 (encoding PD-L1) expression. In the pathway analyses, the solid type was significantly related to high vascular endothelial growth factor (VEGF)-A expression, reflecting tumor angiogenesis. Non-necrosis/low immune response affected by high VEGF-A was associated with worse prognosis. The solid type associated with high VEGF-A expression may contribute to the development of therapeutic strategies for lung adenocarcinoma.
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页数:9
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