Acute Myeloid Leukemia Expresses a Specific Group of Olfactory Receptors.
Gabriela D A GuardiaRafaella G NaressiVanessa C BuzzatoJuliana B da CostaIlana ZalcbergJordana RamiresBettina MalnicLuciana M GutiyamaPedro Alexandre Favoretto GalantePublished in: Cancers (2023)
Acute myeloid leukemia (AML) is the most common form of acute leukemia in adults, with a 5-year overall survival rate of approximately 30%. Despite recent advances in therapeutic options, relapse remains the leading cause of death and poor survival outcomes. New drugs benefit specific small subgroups of patients with actionable therapeutic targets. Thus, finding new targets with greater applicability should be pursued. Olfactory receptors (ORs) are seven transmembrane G-protein coupled receptors preferentially expressed in sensory neurons with a critical role in recognizing odorant molecules. Recent studies have revealed ectopic expression and putative function of ORs in nonolfactory tissues and pathologies, including AML. Here, we investigated OR expression in 151 AML samples, 6400 samples of 15 other cancer types, and 11,200 samples of 51 types of healthy tissues. First, we identified 19 ORs with a distinct and major expression pattern in AML, which were experimentally validated by RT-PCR in an independent set of 13 AML samples, 13 healthy donors, and 8 leukemia cell lines. We also identified an OR signature with prognostic potential for AML patients. Finally, we found cancer-related genes coexpressed with the ORs in the AML samples. In summary, we conducted an extensive study to identify ORs that can be used as novel biomarkers for the diagnosis of AML and as potential drug targets.
Keyphrases
- acute myeloid leukemia
- allogeneic hematopoietic stem cell transplantation
- poor prognosis
- gene expression
- papillary thyroid
- squamous cell carcinoma
- end stage renal disease
- binding protein
- long non coding rna
- spinal cord
- human health
- peritoneal dialysis
- mass spectrometry
- acute lymphoblastic leukemia
- lymph node metastasis
- single cell
- climate change
- childhood cancer
- prognostic factors