hsa_circ_0007841: A Novel Potential Biomarker and Drug Resistance for Multiple Myeloma

Meng Gao1, Chengyuan Li1, Han Xiao1

  • 1The Third Xiangya Hospital of Central South University, Changsha, China.

Frontiers in Oncology
|December 6, 2019
PubMed

Insights

Circular RNA (circRNA) hsa_circ_0007841 is upregulated in multiple myeloma (MM), correlating with poor prognosis and specific genetic aberrations. This finding suggests hsa_circ_0007841 as a potential biomarker for MM.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Circular RNAs (circRNAs) are crucial regulators in tumor development.
  • The role of most circRNAs in cancer, including multiple myeloma (MM), is largely unknown.
  • Understanding circRNA mechanisms is vital for cancer research.

Purpose of the Study:

  • To identify differentially expressed circRNAs in multiple myeloma (MM) using high-throughput circRNA microarray and bioinformatics.
  • To investigate the expression and clinical significance of hsa_circ_0007841 in MM patients.
  • To assess hsa_circ_0007841 as a potential biomarker and therapeutic target in MM.

Main Methods:

  • High-throughput circRNA microarray and bioinformatics analysis.
  • Expression analysis of hsa_circ_0007841 in MM tissues and cell lines.
  • Correlation analysis between hsa_circ_0007841 expression and pathological features, including drug resistance and genetic aberrations.

Main Results:

  • hsa_circ_0007841 was significantly upregulated in MM cell lines and drug-resistant cell lines.
  • Upregulation of hsa_circ_0007841 correlated with disease prognosis and specific genetic alterations (gain 1q21, t(4:14), ATR/IRF4 mutations).
  • Bioinformatics identified interactions between hsa_circ_0007841, miRNAs, and candidate mRNAs.

Conclusions:

  • This study is the first to report significant upregulation of hsa_circ_0007841 in multiple myeloma (MM).
  • hsa_circ_0007841 may serve as a novel biomarker for MM diagnosis and prognosis.
  • hsa_circ_0007841 is implicated in the progression of multiple myeloma.

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