Absence of TSG101 transcript abnormalities in human cancers

Barry Trink, Sara I. Pai, Sheri L. Spunt, Venu Raman, Paul Cairns, Jin Jen, Ed Gabrielson, Saraswati Sukumar, David Sidransky

Research output: Contribution to journalArticlepeer-review

11 Scopus citations


The human TSG101 gene was cloned and mapped to chromosome 11p15, a site suspected to contain a tumor suppressor gene involved in a variety of human cancers. Subsequent investigation described the presence of abnormally spliced transcripts and point mutations of TSG101 in breast cancer. Thus, we performed RT-PCR amplification of the entire open reading frame of TSG101 to test for aberrant transcripts in various human tumor cell lines derived from breast, bladder, head and neck, and lung cancer. In addition, we performed RT-PCR on cDNA from primary human breast and Wilms' tumor tissue. We found a single band of the expected size in 10 of 11 breast cancers and 6 of 6 Wilms' tumor samples after the first round of PCR. The remaining breast cancer sample displayed a barely visible smaller band. However, aberrant bands appeared in most cases after performing nested PCR casting doubt on the physiologic relevance of these spliced variants. We then searched for small intragenic mutations by complete sequence analysis of TSG101 in breast cancer cell lines and tumors, as well as in Wilms' tumors and normal fetal and adult kidney. No point mutations were found in any of the samples, including four breast tumors with chormosomal loss at 11p15. We found no consistent evidence of aberrant splicing or point mutations in breast cancer or Wilms' tumor suggesting that TSG101 is not a primary target of inactivation in human cancer.

Original languageEnglish (US)
Pages (from-to)2815-2818
Number of pages4
Issue number21
StatePublished - May 28 1998


  • Breast cancer
  • RT-PCR
  • TSG101
  • Wilms' tumor

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research


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