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It Takes Two to Tango: Potential Prognostic Impact of Circulating TGF-Beta and PD-L1 in Pancreatic Cancer.
Garajová, Ingrid; Cavazzoni, Andrea; Verze, Michela; Minari, Roberta; Pedrazzi, Giuseppe; Balsano, Rita; Gelsomino, Fabio; Valle, Raffaele Dalla; Digiacomo, Graziana; Giovannetti, Elisa; Leonardi, Francesco.
Afiliação
  • Garajová I; Medical Oncology Unit, University Hospital of Parma, 43126 Parma, Italy.
  • Cavazzoni A; Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.
  • Verze M; Medical Oncology Unit, University Hospital of Parma, 43126 Parma, Italy.
  • Minari R; Medical Oncology Unit, University Hospital of Parma, 43126 Parma, Italy.
  • Pedrazzi G; Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.
  • Balsano R; Medical Oncology Unit, University Hospital of Parma, 43126 Parma, Italy.
  • Gelsomino F; Lab of Medical Oncology, Department of Medical Oncology, Cancer Center Amsterdam, Amsterdam UMC, VU University Medical Center (VUmc), 1081 HV Amsterdam, The Netherlands.
  • Valle RD; Department of Oncology and Hematology, University Hospital of Modena, 41125 Modena, Italy.
  • Digiacomo G; Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.
  • Giovannetti E; Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.
  • Leonardi F; Lab of Medical Oncology, Department of Medical Oncology, Cancer Center Amsterdam, Amsterdam UMC, VU University Medical Center (VUmc), 1081 HV Amsterdam, The Netherlands.
Life (Basel) ; 12(7)2022 Jun 26.
Article em En | MEDLINE | ID: mdl-35888050
Background: Pancreatic ductal adenocarcinoma (PDAC) is a highly devastating disease with rising incidence and poor prognosis. The lack of reliable prognostic biomarkers hampers the individual evaluation of the survival and recurrence potential. Methods: Here, we investigate the value of plasma levels of two potential key players in molecular mechanisms underlying PDAC aggressiveness and immune evasion, soluble TGF-beta (sTGF-beta) and sPD-L1, in both metastatic and radically-resected PDAC. To this aim we prospectively enrolled 38 PDAC patients and performed appropriate statistical analyses in order to evaluate their correlation, and role in the prediction of disease relapse/progression, and patients' outcome. Results: Metastatic patients showed lower levels of circulating sTGF-beta and higher levels of sPD-L1 compared to radically-resected patients. Moreover, a decrease in sTGF-beta levels (but not sPD-L1) was significantly associated with disease relapse in radically-resected patients. We also observed lower sTGF-beta at disease progression after first-line chemotherapy in metastatic patients, though this change was not statistically significant. We found a significant correlation between the levels of sTGF-beta and sPD-L1 before first-line chemotherapy. Conclusions: These findings support the possible interaction of TGF-beta and PD-L1 pathways and suggest that sTGF-beta and sPD-L1 might synergize and be new potential blood-based biomarkers.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article