Proteomic profiling of Trastuzumab (Herceptin(R))-sensitive and -resistant SKBR-3 breast cancer cells.

Ida Pucci, Maria Rita Marabeti, Patrizia Cancemi, Gianluca Di Cara, Nadia Ninfa Albanese, Maria Rita Marabeti, Rosa Musso, Gianluca Di Cara, Germana Marengo, Ida Pucci-Minafra, Patrizia Cancemi, Gianluca Di Cara, Nadia Ninfa Albanese, Rosa Musso

Risultato della ricerca: Articlepeer review

18 Citazioni (Scopus)

Abstract

BACKGROUND:The Human Epidermal Growth Factor Receptor 2 (HER-2), overexpressed in 25-30% of breast carcinomas (BC), is the therapeutic target for trastuzumab, a recombinant humanized monoclonal antibody. The initial response to trastuzumab is often followed by drug-insensitivity within one year. Several hypotheses have been raised to explain this event, but the mechanisms behind the responses to trastuzumab are still unclear. Aim: To study the effects of short and prolonged trastuzumab treatment on the proteomic profiles of HER-2-overexpressing SKBR-3 BC cells.MATERIALS AND METHODS:Cells were treated with trastuzumab to obtain sensitive and resistant clones. The drug effects were evaluated at the phenotypical and proteomic levels.RESULTS:In the trastuzumab-resistant cells the expression of a large amount of proteins, initially affected by treatment, reverted to levels of the untreated cells.CONCLUSION:The results obtained so far illustrate for the first time a large-scale differential protein expression between trastuzumab-treated and untreated cells, and between trastuzumab-sensitive and resistant cells. We believe that the results obtained will help to increase the knowledge of the molecular effects of trastuzumab and will be useful to better-understand the drug resistance mechanisms.
Lingua originaleEnglish
pagine (da-a)489-503
Numero di pagine15
RivistaAnticancer Research
Volume33
Stato di pubblicazionePublished - 2013

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

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