Journal of Translational Medicine (Apr 2008)

The pituitary tumor transforming gene 1 (PTTG-1): An immunological target for multiple myeloma

  • Gagliano Nicoletta,
  • Moreno Jorge,
  • Baggoni Luigi,
  • Yu Yuefei,
  • Prabhakar Madhavi,
  • Ferrari Raffaele,
  • Chiriva-Internati Maurizio,
  • Portinaro Nicola,
  • Jenkins Marjorie R,
  • Frezza Eldo E,
  • Hardwicke Fred,
  • D'Cunha Nicholas,
  • Kast W,
  • Cobos Everardo

DOI
https://doi.org/10.1186/1479-5876-6-15
Journal volume & issue
Vol. 6, no. 1
p. 15

Abstract

Read online

Abstract Background Multiple Myeloma is a cancer of B plasma cells, which produce non-specific antibodies and proliferate uncontrolled. Due to the potential relapse and non-specificity of current treatments, immunotherapy promises to be more specific and may induce long-term immunity in patients. The pituitary tumor transforming gene 1 (PTTG-1) has been shown to be a novel oncogene, expressed in the testis, thymus, colon, lung and placenta (undetectable in most other tissues). Furthermore, it is over expressed in many tumors such as the pituitary adenoma, breast, gastrointestinal cancers, leukemia, lymphoma, and lung cancer and it seems to be associated with tumorigenesis, angiogenesis and cancer progression. The purpose was to investigate the presence/rate of expression of PTTG-1 in multiple myeloma patients. Methods We analyzed the PTTG-1 expression at the transcriptional and the protein level, by PCR, immunocytochemical methods, Dot-blot and ELISA performed on patient's sera in 19 multiple myeloma patients, 6 different multiple myeloma cell lines and in normal human tissue. Results We did not find PTTG-1 presence in the normal human tissue panel, but PTTG-1 mRNA was detectable in 12 of the 19 patients, giving evidence of a 63% rate of expression (data confirmed by ELISA). Four of the 6 investigated cell lines (66.6%) were positive for PTTG-1. Investigations of protein expression gave evidence of 26.3% cytoplasmic expression and 16% surface expression in the plasma cells of multiple myeloma patients. Protein presence was also confirmed by Dot-blot in both cell lines and patients. Conclusion We established PTTG-1's presence at both the transcriptional and protein levels. These data suggest that PTTG-1 is aberrantly expressed in multiple myeloma plasma cells, is highly immunogenic and is a suitable target for immunotherapy of multiple myeloma.