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The GJB3 correlates with the prognosis, immune cell infiltration, and therapeutic responses in lung adenocarcinoma

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机构: [1]Hebei Med Univ, Hosp 4, Dept Thorac Surg, 12 Jiankang Rd, Shijiazhuang 050011, Hebei, Peoples R China [2]First Affiliated Hosp, Xingtai Med Coll, Dept Thorac Surg, Xingtai 054000, Hebei, Peoples R China [3]Hebei Med Univ, Hosp 4, Dept Oncol, Shijiazhuang 050011, Hebei, Peoples R China [4]Hebei Med Univ, Hosp 4, Dept Thorac Surg, Shijiazhuang 050011, Hebei, Peoples R China [5]Tangshan Normal Univ, Dept Comp Sci & Technol, Tangshan, Hebei, Peoples R China
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关键词: lung adenocarcinoma GJB3 transcription factors hsa-miR-6511b-5p immune drug sensitivity

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Gap junction protein beta 3 (GJB3) has been reported as a tumor suppressor in most tumors. However, its role in lung adenocarcinoma (LUAD) remains unknown. The purpose of this study is to explore the role of GJB3 in the prognosis and tumor microenvironment of LUAD patients. The data used in this study were acquired from The Cancer Genome Atlas, Gene Expression Omnibus, and imvigor210 cohorts. We found that GJB3 expression was increased in LUAD patients and correlated with LUAD stages. LUAD patients with high GJB3 expression exhibited a worse prognosis. A total of 164 pathways were significantly activated in the GJB3 (high) group. GJB3 expression was positively associated with nine transcription factors and might be negatively regulated by hsa-miR-6511b-5p. Finally, we found that immune cell infiltration and immune checkpoint expression were different between the GJB3 (high) and GJB3 (low) groups. In summary. GJB3 demonstrated high expression levels in LUAD patients, and those with elevated GJB3 expression displayed unfavorable prognoses. Additionally, there was a correlation between GJB3 and immune cell infiltration, as well as immune checkpoint expression in LUAD patients

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大类 | 4 区 医学
小类 | 4 区 医学:内科
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大类 | 4 区 医学
小类 | 4 区 医学:内科
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Q2 MEDICINE, GENERAL & INTERNAL

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第一作者机构: [2]First Affiliated Hosp, Xingtai Med Coll, Dept Thorac Surg, Xingtai 054000, Hebei, Peoples R China
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