4.8 Article

Aberrant Overexpression of Satellite Repeats in Pancreatic and Other Epithelial Cancers

Journal

SCIENCE
Volume 331, Issue 6017, Pages 593-596

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1200801

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Funding

  1. Pancreatic Cancer Action Network-American Association for Cancer Research
  2. Warshaw Institute for Pancreatic Cancer Research
  3. Fond. Veronesi
  4. Howard Hughes Medical Institute
  5. National Cancer Institute [CA129933]

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Satellite repeats in heterochromatin are transcribed into noncoding RNAs that have been linked to gene silencing and maintenance of chromosomal integrity. Using digital gene expression analysis, we showed that these transcripts are greatly overexpressed in mouse and human epithelial cancers. In 8 of 10 mouse pancreatic ductal adenocarcinomas (PDACs), pericentromeric satellites accounted for a mean 12% (range 1 to 50%) of all cellular transcripts, a mean 40-fold increase over that in normal tissue. In 15 of 15 human PDACs, alpha satellite transcripts were most abundant and HSATII transcripts were highly specific for cancer. Similar patterns were observed in cancers of the lung, kidney, ovary, colon, and prostate. Derepression of satellite transcripts correlated with overexpression of the long interspersed nuclear element 1 (LINE-1) retrotransposon and with aberrant expression of neuroendocrine-associated genes proximal to LINE-1 insertions. The overexpression of satellite transcripts in cancer may reflect global alterations in heterochromatin silencing and could potentially be useful as a biomarker for cancer detection.

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