AI Article Synopsis

  • Researchers studied a family of genes called RUNX to see how they relate to kidney cancer (KIRC).
  • They found that patients with KIRC have higher levels of three specific RUNX genes (RUNX1, RUNX2, RUNX3) and that this could affect their chances of recovery.
  • The study suggests that these RUNX genes are important for understanding how the immune system reacts to the cancer and could lead to new insights into treating KIRC.

Article Abstract

Background: Abnormally expressed Runt-associated transcription factor (RUNX) family has been reported in multiple tumors. Nevertheless, the immunological role of RUNX family in kidney renal clear cell carcinoma (KIRC) remains unknown.

Methods: We studied the RNA-seq data regarding tumor and healthy subjects from several public databases in detail for evaluating the prognostic and immunological functions owned by three RUNX genes in cancer patients. Quantitative real-time reverse transcription-polymerase chain reaction (qRT-PCR) and immunohistochemical (IHC) staining served for detecting their expressions in tumor and normal samples.

Results: We observed that KIRC patients presented high expressions of RUNX1, RUNX2, and RUNX3. The expressions of three genes were validated by qRT-PCR, which was same as bioinformatical results. Prognostic analysis indicated that the overexpression of RUNX1 and RUNX2 negatively affects the outcomes in patients with KIRC. Related functional predictions indicated that the RUNXs and co-expression genes were significantly related to the immune response pathway. Moreover, three RUNX members were associated with immune infiltration cells and their related gene markers. The expression of RUNX family in several immune cells is positively or negatively correlated, and its dysregulation is obviously associated with the differential distribution of immune cells. RUNX family genes were abnormally expressed in KIRC patients, and were closely related to the crosstalk of immune cells.

Conclusions: Our findings may help to understand the pathogenesis and immunologic roles of the RUNX family in KIRC patients from new perspectives.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11066633PMC
http://dx.doi.org/10.1016/j.heliyon.2024.e29870DOI Listing

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