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FOXD1 Is a Transcription Factor Important for Uveal Melanocyte Development and Associated with High-Risk Uveal Melanoma.

Quincy C C van den BoschJosephine Q N NguyenTom BrandsThierry P P van den BoschRobert M VerdijkDion ParidaensNicole C NausAnnelies de KleinEmine KiliçErwin Brosensnull null
Published in: Cancers (2022)
Uveal melanoma (UM) is a deadly ocular malignancy, originating from uveal melanocytes. Although much is known regarding prognostication in UM, the exact mechanism of metastasis is mostly unknown. Metastatic tumor cells are known to express a more stem-like RNA profile which is seen often in cell-specific embryonic development to induce tumor progression. Here, we identified novel transcription regulators by reanalyzing publicly available single cell RNA sequencing experiments. We identified five transcription regulators of interest: ELL2 , KDM5B , REXO4 , RBFOX2 and FOXD1 . Our most significant finding is FOXD1 , as this gene is nearly exclusively expressed in high-risk UM and its expression is associated with a poor prognosis. Even within the BAP1 -mutated UM, the expression of FOXD1 is correlated with poor survival. FOXD1 is a novel factor which could potentially be involved in the metastatic capacity of high-risk UM. Elucidating the function of FOXD1 in UM could provide insight into the malignant transformation of uveal melanocytes, especially in high-risk UM.
Keyphrases
  • poor prognosis
  • transcription factor
  • single cell
  • long non coding rna
  • squamous cell carcinoma
  • small cell lung cancer
  • high throughput
  • dna binding
  • genome wide identification
  • bone marrow