RBSP3 (HYA22) is a tumor suppressor gene implicated in major epithelial malignancies

  • Vladimir I. Kashuba
  • , Jingfeng Li
  • , Fuli Wang
  • , Vera N. Senchenko
  • , Alexey Protopopov
  • , Alena Malyukova
  • , Alexey S. Kutsenko
  • , Elena Kadyrova
  • , Veronika I. Zabarovska
  • , Olga V. Muravenko
  • , Alexander V. Zelenin
  • , Lev L. Kisselev
  • , Igor Kuzmin
  • , John D. Minna
  • , Gösta Winberg
  • , Ingemar Ernberg
  • , Eleonora Braga
  • , Michael I. Lerman
  • , George Klein
  • , Eugene R. Zabarovsky

Research output: Contribution to journalArticlepeer-review

84 Scopus citations

Abstract

Chromosome 3p21.3 region is frequently (>90%) deleted in lung and other major human carcinomas. We subdivided 3p21.3 into LUCA and AP20 subregions and discovered frequent homozygous deletions (10-18%) in both subregions. This finding strongly implies that they harbor multiple tumor suppressor genes involved in the origin and/or development of major epithelial cancers. In this study, we performed an initial analysis of RBSP3/HYA22, a candidate tumor suppressor genes located in the AP20 region. Two sequence splice variants of RBSP3/HYA22 (A and B) were identified, and we provide evidence for their tumor suppressor function. By sequence analysis RBSP3/HYA22 belongs to a gene family of small C-terminal domain phosphatases that may control the RNA polymerase II transcription machinery. Expression of the gene was drastically (>20-fold) decreased in 11 of 12 analyzed carcinoma cell lines and in three of eight tumor biopsies. We report missense and nonsense mutations in tumors where RBSP3/HYA22 was expressed, growth suppression with regulated transgenes in culture, suppression of tumor formation in severe combined immunodeficient mice, and dephosphorylation of ppRB by RBSP3/HYA22, presumably leading to a block of the cell cycle at the G1/S boundary.

Original languageEnglish
Pages (from-to)4906-4911
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume101
Issue number14
DOIs
StatePublished - 6 Apr 2004
Externally publishedYes

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