MicroRNAs as Potential Biomarkers in the Differential Diagnosis of Lipomatous Tumors and Their Mimics

Int J Mol Sci. 2022 Jul 15;23(14):7804. doi: 10.3390/ijms23147804.

Abstract

Adipocytic tumors are the most common subtype of soft tissue tumors. In current clinical practice, distinguishing benign lipomas from well-differentiated liposarcomas (WDLPS), as well as dedifferentiated liposarcomas (DDLPS) from their morphologic mimics, remains a significant diagnostic challenge. This is especially so when examining small biopsy samples and without the aid of additional ancillary tests. Recognizing the important role that microRNAs (miRNAs) play in tumorigenesis and their potential utility in tumor classification, we analyzed routine clinical tissue samples of benign and malignant lipomatous tumors, as well as other sarcoma mimics, to identify distinguishing miRNA-based signatures that can aid in the differential diagnosis of these entities. We discovered a 6-miRNA signature that separated lipomas from WDLPS with high confidence (AUC of 0.963), as well as a separate 6-miRNA signature that distinguished DDLPS from their more aggressive histologic mimics (AUC of 0.740). Functional enrichment analysis unveiled possible mechanistic involvement of these predictive miRNAs in adipocytic cancer-related biological processes and pathways such as PI3K/AKT/mTOR and MAPK signaling, further supporting the relevance of these miRNAs as biomarkers for adipocytic tumors. Our results demonstrate that miRNA expression profiling may potentially be used as an adjunctive tool for the diagnosis of benign and malignant adipocytic tumors. Further validation studies are warranted.

Keywords: dedifferentiated liposarcoma; lipoma; microRNA; undifferentiated pleomorphic sarcoma; well-differentiated liposarcoma.

MeSH terms

  • Biomarkers, Tumor / analysis
  • Biomarkers, Tumor / genetics
  • Diagnosis, Differential
  • Humans
  • Lipoma* / diagnosis
  • Lipoma* / genetics
  • Liposarcoma* / diagnosis
  • Liposarcoma* / genetics
  • Liposarcoma* / pathology
  • MicroRNAs* / genetics
  • Phosphatidylinositol 3-Kinases
  • Soft Tissue Neoplasms* / pathology

Substances

  • Biomarkers, Tumor
  • MicroRNAs