MRPL12 Acts as A Novel Prognostic Biomarker Involved in Immune Cell Infiltration and Tumor Progression of Lung

Yangyang Hu1, Yue Liu1, Chenchao Ma1

  • 1Department of Thoracic Surgery, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai 200433, China.

Insights

Mitochondrial ribosomal protein L7/L12 (MRPL12) is elevated in lung adenocarcinoma (LUAD), correlating with poor prognosis and influencing immune cell infiltration. Targeting MRPL12 may offer a new therapeutic strategy for LUAD patients.

Area of Science:

  • Molecular Biology
  • Oncology
  • Immunology

Background:

  • Mitochondrial ribosomal proteins (MRPs) play crucial roles in cellular functions.
  • The specific role of Mitochondrial ribosomal protein L7/L12 (MRPL12) in lung adenocarcinoma (LUAD) is not well understood.

Purpose of the Study:

  • To investigate the expression, prognostic value, and biological function of MRPL12 in LUAD.
  • To explore the association between MRPL12 and immune infiltrates in LUAD.
  • To evaluate MRPL12 as a potential therapeutic target for LUAD.

Main Methods:

  • Bioinformatic analysis using UALCAN, TIMER, HPA, Kaplan-Meier plotter, and GEPIA databases.
  • Investigation of MRPL12 and immune infiltrates using TIMER and TISIDB databases.
  • Validation of clinical significance via tissue microarray (TMA) and functional experiments (MRPL12 knockdown).

Main Results:

  • MRPL12 was significantly upregulated in LUAD tissues compared to normal tissues.
  • High MRPL12 expression was associated with unfavorable prognosis and identified as an independent prognostic factor.
  • MRPL12 expression correlated with immunomodulators, chemokines, and the infiltration of various immune cells.
  • MRPL12 knockdown suppressed LUAD cell proliferation, migration, and invasion.

Conclusions:

  • MRPL12 serves as a potential prognostic biomarker in LUAD.
  • MRPL12 expression is linked to the tumor immune microenvironment in LUAD.
  • MRPL12 represents a promising therapeutic target for lung adenocarcinoma.