Overexpression of BCCIP predicts an unfavorable prognosis and promotes the proliferation and migration of lung adenocarcinoma. Issue 17 (23rd July 2021)

• Record Type: Journal Article
• Authors: Shi, Jie; Lv, Xin; Li, Wei; Ming, Zongjuan; Zeng, Lizhong; Yuan, Jingyan; Chen, Yang; Liu, Boxuan; Yang, Shuanying
• Is Part Of: Thoracic cancer. Volume 12:Issue 17(2021)
• Page Start: 2324
• Page End: 2338
• Publication Date: 2021-07-23
• Subjects: BCCIP -- immune infiltration -- lung adenocarcinoma -- migration -- proliferation -- tumor microenvironment; Chest -- Cancer -- Periodicals; Chest -- Cancer -- Treatment -- Periodicals; Chest -- Surgery -- Periodicals; 616.99494005
• DOI: 10.1111/1759-7714.14073
• Languages: English
• ISSNs: 1759-7706

Abstract

Abstract: Background: Lung cancer accounts for the highest rate of cancer‐related diagnosis and mortality. Lung adenocarcinoma (LUAD) is the most common histopathological type. BCCIP was originally identified as a BRCA2 and CDKN1A interacting protein. In different cancers, BCCIP plays different roles. The role of BCCIP in LUAD is still unknown. Methods: The expression and prognostic value of BCCIP was analyzed using public databases, including LCE, GEPIA, TCGA, and clinical specimens. Bioinformatic analysis and vitro experiments were conducted to explore the biological functions of BCCIP in LUAD. By using the GEPIA and TIMER databases, we investigated the correlations between LUAD expression and immune infiltration in LUAD. Results: Compared with normal tissue, LUAD tissue had a higher expression level of BCCIP and high expression level of BCCIP was detrimental to LUAD patient survival. The suppression of BCCIP inhibited LUAD cell proliferation, migration and resulted in G1/S phase arrest in vitro. Bioinformatic analysis demonstrated that BCCIP could be associated with cell cycle, DNA repair and E2F transcription factor family. There were significant correlations between BCCIP expression and immune infiltrates, including B cell, CD4+ T cell, macrophage, neutrophil and dendritic cells. Furthermore, BCCIP expression showed strong correlations with diverse immune marker sets in LUAD, such as B cell, macrophage and DC. Conclusions: Overexpression of BCCIP predicts an unfavorable prognosis and promotes the proliferation and migration of lung adenocarcinoma cells. BCCIP is correlated with immune infiltration in LUAD. Suppression of BCCIP may be a potential approach in the prevention and treatment of LUAD. Abstract : In different cancers, BCCIP plays different roles. However, the role of BCCIP in LUAD is still unknown. Using bioinformatic analysis, clinical data and vitro experiments, we found that high BCCIP expression promotes the proliferation and migration of LUAD cells and was associated with an unfavorable prognosis and immune infiltration through regulating the cell cycle, DNA repair and E2F transcription factor family.