α-Synuclein (-syn) is a protein involved in neuronal degeneration. However, the family of synucleins has recently been demonstrated to be involved in the mechanisms of oncogenesis by selectively accelerating cellular processes leading to cancer. Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal human cancers, with a specifically high neurotropism. The molecular bases of this biological behavior are currently poorly understood. Here, -synuclein was analyzed concerning the protein expression in PDAC and the potential association with PDAC neurotropism. Tumor (PDAC) and extra-tumor (extra-PDAC) samples from 20 patients affected by PDAC following pancreatic resections were collected at the General Surgery Unit, University of Pisa. All patients were affected by moderately or poorly differentiated PDAC. The amount of -syn was compared between tumor and extra-tumor specimen (sampled from non-affected neighboring pancreatic areas) by using in situ immuno-staining with peroxidase anti--syn immunohistochemistry, -syn detection by using Western blotting, and electron microscopy by using -syn-conjugated immuno-gold particles. All the methods consistently indicate that each PDAC sample possesses a higher amount of -syn compared with extra-PDAC tissue. Moreover, the expression of -syn was much higher in those PDAC samples from tumors with perineural infiltration compared with tumors without perineural infiltration.

In Pancreatic Adenocarcinoma Alpha-Synuclein Increases and Marks Peri-Neural Infiltration

Matteo Bianchini;Maria Giambelluca;Maria Concetta Scavuzzo;Gregorio Di Franco;Matteo Palmeri;Niccolò Furbetta;Desirée Gianardi;Manuel Gentiluomo;Raffaele Gaeta;Caterina Vivaldi;Giulio Di Candio;Paola Soldani;Luca Morelli
;
Francesco Fornai
2022-01-01

Abstract

α-Synuclein (-syn) is a protein involved in neuronal degeneration. However, the family of synucleins has recently been demonstrated to be involved in the mechanisms of oncogenesis by selectively accelerating cellular processes leading to cancer. Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal human cancers, with a specifically high neurotropism. The molecular bases of this biological behavior are currently poorly understood. Here, -synuclein was analyzed concerning the protein expression in PDAC and the potential association with PDAC neurotropism. Tumor (PDAC) and extra-tumor (extra-PDAC) samples from 20 patients affected by PDAC following pancreatic resections were collected at the General Surgery Unit, University of Pisa. All patients were affected by moderately or poorly differentiated PDAC. The amount of -syn was compared between tumor and extra-tumor specimen (sampled from non-affected neighboring pancreatic areas) by using in situ immuno-staining with peroxidase anti--syn immunohistochemistry, -syn detection by using Western blotting, and electron microscopy by using -syn-conjugated immuno-gold particles. All the methods consistently indicate that each PDAC sample possesses a higher amount of -syn compared with extra-PDAC tissue. Moreover, the expression of -syn was much higher in those PDAC samples from tumors with perineural infiltration compared with tumors without perineural infiltration.
2022
Bianchini, Matteo; Giambelluca, Maria; Scavuzzo, MARIA CONCETTA; DI FRANCO, Gregorio; Guadagni, Simone; Palmeri, Matteo; Furbetta, Niccolò; Gianardi, Desirée; Costa, Aurelio; Gentiluomo, Manuel; Gaeta, Raffaele; Emanuele Pollina, Luca; Falcone, Alfredo; Vivaldi, Caterina; DI CANDIO, Giulio; Biagioni, Francesca; Letizia Busceti, Carla; Soldani, Paola; Puglisi-Allegra, Stefano; Morelli, Luca; Fornai, Francesco
File in questo prodotto:
File Dimensione Formato  
ijms-Bianchini et al.pdf

accesso aperto

Tipologia: Versione finale editoriale
Licenza: Creative commons
Dimensione 5.8 MB
Formato Adobe PDF
5.8 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/1142067
Citazioni
  • ???jsp.display-item.citation.pmc??? 2
  • Scopus 4
  • ???jsp.display-item.citation.isi??? 4
social impact