Establishment of a cell line from a malignant rhabdoid tumor of the liver lacking the function of two tumor suppressor genes, hSNF5/INI1 and p16

Cancer Genet Cytogenet. 2005 Apr 15;158(2):172-9. doi: 10.1016/j.cancergencyto.2004.08.032.

Abstract

Malignant rhabdoid tumors (MRT) of the liver are rare. A few liver MRT cell lines have been established but none has been characterized in detail. Here we describe a new MRT cell line from the liver, which is designated MP-MRT-AN, and describe it in detail. Immunohistochemical assays detected the expression of vimentin and cytokeratin but they were negative for neurofilament, desmin, alpha-smooth muscle actin, alpha-sarcomeric actin, and smooth muscle myosin heavy chains SM1 and SM2. RT-PCR assays revealed that this cell line did not express smooth muscle myosin heavy chain isoforms or MyoD1. No aberration was identified in 22q by G-banded analysis; however, the hSNF5/INI1 gene, a suppressor gene of MRT that maps to 22q11.2, was homozygously deleted from exons 1 to 5 in this cell line. Furthermore, the expression of another tumor suppressor gene, p16 (CDKN2A), was not detected by RT-PCR. This raises the possibility that the aggressive phenotype of malignant rhabdoid tumors is caused by the loss of two or more tumor suppressor genes.

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Chromosomal Proteins, Non-Histone
  • Chromosome Banding
  • Chromosome Mapping
  • Chromosomes, Human, Pair 22
  • DNA-Binding Proteins / genetics*
  • Female
  • Gene Deletion*
  • Genes, Tumor Suppressor*
  • Genes, p16*
  • Homozygote
  • Humans
  • Immunohistochemistry
  • Infant
  • Keratins / metabolism
  • Liver Neoplasms / diagnosis
  • Liver Neoplasms / diagnostic imaging
  • Liver Neoplasms / pathology*
  • Liver Neoplasms / surgery
  • Mice
  • Mice, Nude
  • Neoplasm Transplantation
  • Reverse Transcriptase Polymerase Chain Reaction
  • Rhabdoid Tumor / diagnosis
  • Rhabdoid Tumor / diagnostic imaging
  • Rhabdoid Tumor / genetics*
  • Rhabdoid Tumor / metabolism
  • Rhabdoid Tumor / pathology
  • SMARCB1 Protein
  • Transcription Factors / genetics*
  • Ultrasonography
  • Vimentin / metabolism

Substances

  • Chromosomal Proteins, Non-Histone
  • DNA-Binding Proteins
  • SMARCB1 Protein
  • SMARCB1 protein, human
  • Smarcb1 protein, mouse
  • Transcription Factors
  • Vimentin
  • Keratins