Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2023 Jan 4;13:991604. doi: 10.3389/fimmu.2022.991604

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

Copyright © 2023 Li, Jin, Chen, Zhang, Li, Zhong, Fan and Lin

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

PMC Copyright notice

Relationship between the lncRNA-based signature and immune responses in HCC. (A) Relative proportion of 22 different immune cells based on CIBERSORT in the low-risk group and the high-risk group. Immune cells in red indicated that there was a significant difference within the two groups. (B-I) The proportion of M0 macrophages, neutrophil, activated memory CD4+ T cells, follicular helper T cells, regulatory T cells, activated mast cell, monocyte and resting memory CD4+ T cells in the low-risk group and the high-risk group. (J) Heat map showing the relations between risk score and various immune checkpoints via Pearson test. (K) PDCD1 and CD274 were significantly upregulated in the high-risk group. lncRNAs, long noncoding RNAs; HCC, hepatocellular carcinoma. *p < 0.05, **p < 0.01, and ***p < 0.001.