miR-150 is a negative independent prognostic biomarker for primary gastrointestinal diffuse large B-cell lymphoma

Xinyuan Wang1, Yutian Kan1, Leiyuan Chen1

  • 1Department of Hematology and Oncology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin Clinical Research Center for Cancer, Tianjin 300060, P.R. China.

Oncology Letters
|April 10, 2020
PubMed

Insights

This study reveals that microRNA (miR-150) is significantly lower in primary gastrointestinal diffuse large B-cell lymphoma (PGI-DLBCL) tissues. Low miR-150 expression serves as a potential diagnostic marker and prognostic factor for PGI-DLBCL patient survival.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Diffuse large B-cell lymphoma (DLBCL) is a heterogeneous hematologic malignancy.
  • MicroRNAs (miRNAs) play crucial roles in lymphomagenesis and have emerged as potential biomarkers.
  • Primary gastrointestinal DLBCL (PGI-DLBCL) presents unique clinical challenges and prognostic factors.

Purpose of the Study:

  • To investigate the prognostic value of microRNA (miR-150) in patients with PGI-DLBCL.
  • To assess the association between miR-150 expression levels and clinicopathological characteristics.
  • To evaluate miR-150 as a potential diagnostic and prognostic biomarker for PGI-DLBCL.

Main Methods:

  • Retrospective analysis of 84 PGI-DLBCL patients.
  • Quantification of miR-150 expression in tumor and adjacent non-tumor tissues using reverse transcription-quantitative PCR (RT-qPCR).
  • Correlation analysis between miR-150 levels, clinicopathological features, and survival outcomes (Overall Survival - OS, Progression-Free Survival - PFS).
  • Receiver Operating Characteristic (ROC) curve analysis for diagnostic and prognostic value assessment.

Main Results:

  • miR-150 expression was significantly lower in PGI-DLBCL tissues compared to non-tumor tissues.
  • Low miR-150 expression correlated with advanced clinical stage, higher International Prognostic Index (IPI) scores, poorer Eastern Cooperative Oncology Group (ECOG) status, and rituximab use.
  • Downregulated miR-150 was significantly associated with shorter OS and PFS.
  • ROC analysis indicated miR-150 as a potential diagnostic marker (Area Under Curve = 0.882) and prognostic factor.

Conclusions:

  • miR-150 is significantly downregulated in PGI-DLBCL.
  • Low miR-150 expression is a potential diagnostic biomarker for PGI-DLBCL.
  • miR-150 serves as a valuable prognostic factor for survival outcomes in PGI-DLBCL patients, independent of IPI score.

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