Objective To investigate the correlation between regulator of G protein signaling 22 (RGS22) and immune cell infiltration in lung adenocarcinoma (LUAD) through bioinformatics analysis, it is to identify novel potential biomarkers for auxiliary diagnosis and therapy. Methods Gene expression data and relevant clinical data were downloaded from The Cancer Genome Atlas (TCGA) database to analyze the correlation between RGS22 expression and tumor immune cell infiltration in LUAD. In addition, external validation in an independent cohort was performed using public datasets from the Gene Expression Omnibus (GEO). Results The study found that RGS22 was downregulated in LUAD tumor tissues, which was associated with shorter overall survival in patients. This results were validated in both the TCGA cohort (n = 527, P = 0.004) and the GEO cohort (n = 398, P = 3.01×10-6). The expression of RGS22 was positively correlated with the infiltration levels of various immune cells, including dendritic cells and CD4+ T cells. Therefore, these findings revealed that RGS22 influences the prognosis of LUAD by affecting the infiltration levels of immune cells. Conclusion RGS22 maybe become a new biomarker for the early diagnosis and prognosis of LUAD.
| Published in | Science Research (Volume 14, Issue 5) |
| DOI | 10.11648/j.sr.20261405.14 |
| Page(s) | 286-295 |
| Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
| Copyright |
Copyright © The Author(s), 2026. Published by Science Publishing Group |
Lung Adenocarcinoma, Regulator of G-Protein Signaling 22, Bioinformatics, Immune-infiltrating Cells, Prognosis, Biomarker
| [1] | SIEGEL RL, KRATZER TB, GIAQUINTO AN, et al. Cancer statistics, 2025. CA Cancer J Clin. 2025, 75(1): 10-45. |
| [2] | SIEGEL RL, GIAQUINTO AN, JEMAL A. Cancer statistics, 2024. CA Cancer J Clin. 2024, 74(1): 12-49. |
| [3] | BRAY F, LAVERSANNE M, SUNG H, et al. Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries [J]. CA Cancer JClin, 2024, 74(3): 229 -263. |
| [4] | HAN B, ZHENG R, ZENG H, et al. Cancer incidence and mortality in China, 2022 [J]. JNatl Cancer Cent, 2024, 4(1): 47-53. |
| [5] | ZHENG RS, CHEN R, HAN BF, et al. [Cancer incidence and mortality in China, 2022]. Zhonghua Zhong Liu Za Zhi. 2024, 23; 46(3): 221-231. |
| [6] | 肖开禺, 刘新光. 肿瘤-睾丸抗原83在肿瘤中的研究进展 [J]. 微生物学免疫学进展, 2024, 52(05): 86-91. |
| [7] | 江颖锋. 肿瘤睾丸抗原HEMGN在肺腺癌中的表达及其免疫浸润相关性研究 [D]. 福建医科大学, 2023. |
| [8] | MALLA R, SRILATHA M, MUPPALA V, et al. Neoantigens and cancer-testis antigens as promising vaccine candidates for triple-negative breast cancer: delivery strategies and clinical trials [J]. JControl Release, 2024, 370: 707-720. |
| [9] | ZHOU H,MA Y, LIU F, et al. Current advances in cancer vaccines targeting NY - ESO -1 for solid cancer treatment [J]. Front Immunol, 2023, 14: 1255799. |
| [10] | ALSALLOUM A, SHEVCHENKO JA, SENNIKOV S. The melanoma - associated antigen family A (MAGE-A): a promising target for cancer im- munotherapy? [J]. Cancers: Basel, 2023, 15(6): 1779. |
| [11] | 谭媛芳. 肿瘤—睾丸抗原HCA587蛋白疫苗的抗黑色素瘤效应及机制探索 [D]. 南昌大学, 2024. |
| [12] | 陆烨大, 林东子, 吴汝明, 等. 肺癌自身抗体肿瘤/睾丸抗原G抗原7、黑色素瘤抗原A1、神经细胞胞浆蛋白9. 5联合检测对肺癌化疗疗效评估价值研究 [J]. 临床军医杂志, 2024, 52(10): 1073-1076. |
| [13] | 冯振卿. CAR-T细胞技术研究进展及发展趋势 [J]. 南京医科大学学报 (自然科学版), 2020, 40(7): 937-939, 962. |
| [14] | 陈玉凤, 唐奇, 冯振卿. MAGE-A1在肿瘤诊断及免疫治疗中的研究进展 [J]. 河北医科大学学报, 2024, 45(05): 615-621. |
| [15] | 赵振凯, 梁国, 李枫, 等. 胶质母细胞瘤中癌-睾丸抗原OY-TES-1的表达对M2型巨噬细胞极化的影响 [J]. 中国临床新医学, 2024, 17(08): 875-880. |
APA Style
Cuihua, F., Dongbiao, Q., Jiandong, Z. (2026). A Bioinformatics-based Study Investigating the Crrelation Between RGS22 Expression and Immune Cell Infiltration in Lung Adenocarcinoma. Science Research, 14(5), 286-295. https://doi.org/10.11648/j.sr.20261405.14
ACS Style
Cuihua, F.; Dongbiao, Q.; Jiandong, Z. A Bioinformatics-based Study Investigating the Crrelation Between RGS22 Expression and Immune Cell Infiltration in Lung Adenocarcinoma. Sci. Res. 2026, 14(5), 286-295. doi: 10.11648/j.sr.20261405.14
@article{10.11648/j.sr.20261405.14,
author = {Fan Cuihua and Qiu Dongbiao and Zhang Jiandong},
title = {A Bioinformatics-based Study Investigating the Crrelation Between RGS22 Expression and Immune Cell Infiltration in Lung Adenocarcinoma},
journal = {Science Research},
volume = {14},
number = {5},
pages = {286-295},
doi = {10.11648/j.sr.20261405.14},
url = {https://doi.org/10.11648/j.sr.20261405.14},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.sr.20261405.14},
abstract = {Objective To investigate the correlation between regulator of G protein signaling 22 (RGS22) and immune cell infiltration in lung adenocarcinoma (LUAD) through bioinformatics analysis, it is to identify novel potential biomarkers for auxiliary diagnosis and therapy. Methods Gene expression data and relevant clinical data were downloaded from The Cancer Genome Atlas (TCGA) database to analyze the correlation between RGS22 expression and tumor immune cell infiltration in LUAD. In addition, external validation in an independent cohort was performed using public datasets from the Gene Expression Omnibus (GEO). Results The study found that RGS22 was downregulated in LUAD tumor tissues, which was associated with shorter overall survival in patients. This results were validated in both the TCGA cohort (n = 527, P = 0.004) and the GEO cohort (n = 398, P = 3.01×10-6). The expression of RGS22 was positively correlated with the infiltration levels of various immune cells, including dendritic cells and CD4+ T cells. Therefore, these findings revealed that RGS22 influences the prognosis of LUAD by affecting the infiltration levels of immune cells. Conclusion RGS22 maybe become a new biomarker for the early diagnosis and prognosis of LUAD.},
year = {2026}
}
TY - JOUR T1 - A Bioinformatics-based Study Investigating the Crrelation Between RGS22 Expression and Immune Cell Infiltration in Lung Adenocarcinoma AU - Fan Cuihua AU - Qiu Dongbiao AU - Zhang Jiandong Y1 - 2026/09/04 PY - 2026 N1 - https://doi.org/10.11648/j.sr.20261405.14 DO - 10.11648/j.sr.20261405.14 T2 - Science Research JF - Science Research JO - Science Research SP - 286 EP - 295 PB - Science Publishing Group SN - 2329-0927 UR - https://doi.org/10.11648/j.sr.20261405.14 AB - Objective To investigate the correlation between regulator of G protein signaling 22 (RGS22) and immune cell infiltration in lung adenocarcinoma (LUAD) through bioinformatics analysis, it is to identify novel potential biomarkers for auxiliary diagnosis and therapy. Methods Gene expression data and relevant clinical data were downloaded from The Cancer Genome Atlas (TCGA) database to analyze the correlation between RGS22 expression and tumor immune cell infiltration in LUAD. In addition, external validation in an independent cohort was performed using public datasets from the Gene Expression Omnibus (GEO). Results The study found that RGS22 was downregulated in LUAD tumor tissues, which was associated with shorter overall survival in patients. This results were validated in both the TCGA cohort (n = 527, P = 0.004) and the GEO cohort (n = 398, P = 3.01×10-6). The expression of RGS22 was positively correlated with the infiltration levels of various immune cells, including dendritic cells and CD4+ T cells. Therefore, these findings revealed that RGS22 influences the prognosis of LUAD by affecting the infiltration levels of immune cells. Conclusion RGS22 maybe become a new biomarker for the early diagnosis and prognosis of LUAD. VL - 14 IS - 5 ER -