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Update on SWI/SNF-related gynecologic mesenchymal neoplasms: SMARCA4-deficient uterine sarcoma and SMARCB1-deficient vulvar neoplasms.

Brooke E HowittAndrew L Folpe
Published in: Genes, chromosomes & cancer (2020)
Our knowledge regarding the role of genes encoding the chromatin remodeling switch/sucrose non-fermenting (SWI/SNF) complex in the initiation and progression of gynecologic malignancies continues to evolve. This review focuses on gynecologic tumors in which the sole or primary genetic alteration is in SMARCA4 or SMARCB1, two members of the SWI/SNF chromatin remodeling complex. In this review, we present a brief overview of the classical example of such tumors, ovarian small cell carcinoma of hypercalcemic type, and then a detailed review and update of SMARCB1-deficient and SMARCA4-deficient tumors of the uterus and vulva.
Keyphrases
  • genome wide
  • gene expression
  • dna damage
  • transcription factor
  • healthcare
  • endometrial cancer
  • stem cells
  • bone marrow
  • dna methylation
  • wild type
  • lymph node
  • squamous cell carcinoma
  • copy number
  • sentinel lymph node