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Research Paper

Protein phosphatase 1 regulatory subunit 3G (PPP1R3G) correlates with poor prognosis and immune infiltration in lung adenocarcinoma

, , , , , & ORCID Icon show all
Pages 8336-8346 | Received 14 Jul 2021, Accepted 22 Sep 2021, Published online: 21 Oct 2021

Figures & data

Figure 1. PPP1R3G was upregulated in lung adenocarcinoma (LUAD)

(a) PPP1R3G expression levels in diverse kinds of tumors. Data was extracted from The Cancer Genome Atlas (TCGA) database by TIMER.(b) PPP1R3G expression in LUAD tissues compared to that in nonmalignant lung tissues using comparison of samples in TCGA database.(c) PPP1R3G expression pre-disease and post-disease in the same patient.(d) Differential expression of PPP1R3G protein between LUAD and nonmalignant lung tissues in the CPTAC data resource.(e) PPP1R3G expression levels in LUAD tissues and normal lung tissues of mice.
Figure 1. PPP1R3G was upregulated in lung adenocarcinoma (LUAD)

Table 1. Baseline charateristics of patients with LUAD

Figure 2. PPP1R3G mRNA expression in clinical characteristics of lung adenocarcinoma (LUAD) tissue

(a) Differential expression of PPP1R3G mRNA between LUAD and nonmalignant lung tissues in the The Cancer Genome Atlas data resource.(b-d) Comparison of PPP1R3G mRNA expression based on patient’s gender, individual cancer, and nodal metastasis. NA P > 0.05, * P < 0.05; ** P < 0.01; *** P < 0.001.
Figure 2. PPP1R3G mRNA expression in clinical characteristics of lung adenocarcinoma (LUAD) tissue

Figure 3. Prognostic function of PPP1R3G in lung adenocarcinoma

(a) Overall survival analysis of PPP1R3G according to TCGA database.(b) Association of PPP1R3G expression with overall survival of lung adenocarcinoma patients from the UALCAN data resource.
Figure 3. Prognostic function of PPP1R3G in lung adenocarcinoma

Table 2. Univariate analysis and Multivariate analysis of the correlation of PPP1R3G expression with OS among lung adenocarcinoma

Figure 4. The independent prognostic factor and clinical diagnostic value of PPP1R3G in lung adenocarcinoma (LUAD)

(a) Cox multivariate analysis was used to compare clinical characteristics of the forest plots of 316 patients with LUAD.(b) Receiver operating characteristic curve revealed the clinical diagnostic value of PPP1R3G in LUAD.
Figure 4. The independent prognostic factor and clinical diagnostic value of PPP1R3G in lung adenocarcinoma (LUAD)

Figure 5. PPP1R3G relates to immune infiltration level in lung adenocarcinoma (LUAD)

(a) PPP1R3G expression was positively correlated with the infiltration levels of CD4 + T cells, macrophages, neutrophil, neutrophils, and dendritic cells in LUAD.(b) PPP1R3G CNV influences the infiltration level of B cells, CD4 + T cells, macrophages, neutrophils, and dendritic cells in LUAD.
Figure 5. PPP1R3G relates to immune infiltration level in lung adenocarcinoma (LUAD)

Figure 6. Gene enrichment analysis of PPP1R3G in lung adenocarcinoma cohorts

(a-c) Enriched GO terms of PPP1R3G-linked genes.(d). Enriched KEGG cascades of PPP1R3G-related genes.(e).The PPP1R3G-miRNA regulatory network.
Figure 6. Gene enrichment analysis of PPP1R3G in lung adenocarcinoma cohorts
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