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PLOD3 Is Associated with Immune Cell Infiltration and Genomic Instability in Colon Adenocarcinoma.
Deng, Xianyu; Pan, Yun; Yang, Muqing; Liu, Ying; Li, Jiyu.
Afiliación
  • Deng X; Colorectal Cancer Center, Tenth People's Hospital of Tongji University, Tongji University School of Medicine, China.
  • Pan Y; Colorectal Cancer Center, Tenth People's Hospital of Tongji University, Tongji University School of Medicine, China.
  • Yang M; Center for Difficult and Complicated Abdominal Surgery, Tenth People's Hospital of Tongji University, Tongji University School of Medicine, China.
  • Liu Y; Department of General Surgery, Tenth People's Hospital of Tongji University, Tongji University School of Medicine, China.
  • Li J; Colorectal Cancer Center, Tenth People's Hospital of Tongji University, Tongji University School of Medicine, China.
Biomed Res Int ; 2021: 4714526, 2021.
Article en En | MEDLINE | ID: mdl-34239923
Procollagen-lysine, 2-oxoglutarate 5-dioxygenases (PLODs) are a family of enzymes. However, the clinical and functional roles of PLOD3 in colon adenocarcinoma (COAD) have not been investigated. The present study found that PLOD3 was highly upregulated in COAD, which may be resulted from its aberrant DNA methylation. The upregulation of both PLOD3 mRNA and protein was confirmed in our tissue samples. Moreover, high PLOD3 was identified to be associated with unfavorable prognosis in COAD. As genome instability is a hallmark of cancer, PLOD3 was expressed higher in COAD samples with high chromosomal instability (CIN-high) than those with low CIN (CIN-low) and higher in those with low MSI than high MSI, indicating that PLOD3 expression was associated with tumor genomic instability. Furthermore, immune cells showed significantly different infiltrating levels between the high and low PLOD3 expression groups, and the immune score was negatively correlated with PLOD3 expression and higher in samples with low PLOD3 expression, suggesting that high PLOD3 expression was associated with reduced immune cell infiltrating levels in COAD. To further uncover the underlying mechanism of PLOD3 in PLOD3, we compared the COAD samples of high PLOD3 expression with those of low PLOD3 expression and found that high expression of PLOD3 was associated with reduced expression of immune regulators and enhanced activities of two tumor-promoting pathways, including gluconeogenesis and TGF-beta signaling in epithelial-mesenchymal transition (EMT), suggesting that high expression of PLOD3 causes poor prognosis in COAD by weakening the immune cell infiltration and enhancing activities of tumor-promoting pathways. In summary, the present study highlights the importance of PLOD3 and provides the evidence about the functional role of PLOD3 in COAD.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Adenocarcinoma / Regulación Neoplásica de la Expresión Génica / Procolágeno-Lisina 2-Oxoglutarato 5-Dioxigenasa / Neoplasias del Colon Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Biomed Res Int Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Adenocarcinoma / Regulación Neoplásica de la Expresión Génica / Procolágeno-Lisina 2-Oxoglutarato 5-Dioxigenasa / Neoplasias del Colon Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Biomed Res Int Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos