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High PTEN gene expression is a negative prognostic marker in human primary breast cancers with preserved p53 function.
Yndestad, Synnøve; Austreid, Eilin; Knappskog, Stian; Chrisanthar, Ranjan; Lilleng, Peer Kåre; Lønning, Per Eystein; Eikesdal, Hans Petter.
Afiliação
  • Yndestad S; Section of Oncology, Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Austreid E; Department of Oncology, Haukeland University Hospital, Bergen, Norway.
  • Knappskog S; Section of Oncology, Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Chrisanthar R; Section of Oncology, Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Lilleng PK; Department of Oncology, Haukeland University Hospital, Bergen, Norway.
  • Lønning PE; Section of Oncology, Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Eikesdal HP; Section of Molecular Pathology, Department of Pathology, Oslo University Hospital, Oslo, Norway.
Breast Cancer Res Treat ; 163(1): 177-190, 2017 May.
Article em En | MEDLINE | ID: mdl-28213783
ABSTRACT

PURPOSE:

PTEN is an important tumor suppressor in breast cancer. Here, we examined the prognostic and predictive value of PTEN and PTEN pseudogene (PTENP1) gene expression in patients with locally advanced breast cancer given neoadjuvant chemotherapy.

METHODS:

The association between pretreatment PTEN and PTENP1 gene expression, response to neoadjuvant chemotherapy, and recurrence-free and disease-specific survival was assessed in 364 patients with locally advanced breast cancer given doxorubicin, 5-fluorouracil/mitomycin, or epirubicin versus paclitaxel in three phase II prospective studies. Further, protein expression of PTEN or phosphorylated Akt, S6 kinase, and 4EBP1 was assessed in a subgroup of 187 tumors.

RESULTS:

Neither PTEN nor PTENP1 gene expression level predicted response to any of the chemotherapy regimens tested (n = 317). Among patients without distant metastases (n = 282), a high pretreatment PTEN mRNA level was associated with inferior relapse-free (RFS; p = 0.001) and disease-specific survival (DSS; p = 0.003). Notably, this association was limited to patients harboring TP53 wild-type tumors (RFS; p = 0.003, DSS; p = 0.009). PTEN mRNA correlated significantly with PTENP1 mRNA levels (r s = 0.456, p < 0.0001) and PTEN protein staining (r s = 0.163, p = 0.036). However, no correlation between PTEN, phosphorylated Akt, S6 kinase or 4EBP1 protein staining, and survival was recorded. Similarly, no correlation between PTENP1 gene expression and survival outcome was observed.

CONCLUSION:

High intratumoral PTEN gene expression was associated with poor prognosis in patients with locally advanced breast cancers harboring wild-type TP53.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Protocolos de Quimioterapia Combinada Antineoplásica / Proteína Supressora de Tumor p53 / Quimioterapia Adjuvante / PTEN Fosfo-Hidrolase Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Protocolos de Quimioterapia Combinada Antineoplásica / Proteína Supressora de Tumor p53 / Quimioterapia Adjuvante / PTEN Fosfo-Hidrolase Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article