Pancreatic cancer is one of the most deadly forms of cancer because it is often diagnosed too late, when treatments are less effective. Currently, there is no practical way to screen individuals who are at risk but have no symptoms. In this study, we describe a specific genetic variation in a gene called TP53, which is known to play a role in many types of cancer. We found that this variation appears to be more common in people with pancreatic cancer than in the general population. This suggests that individuals carrying this variation may have a higher risk of developing the disease. These findings may help open a new line of research aimed at identifying high-risk populations.
Association of TP53 Arg72Pro (rs1042522) Polymorphism with Pancreatic Cancer Risk in a Patient Cohort / Antolino, Laura; De Nucci, Germana; Scarpino, Stefania; Bianco, Giuseppe; Lopez, Gianluca; Aurello, Paolo; Petrucciani, Niccolò; Santoro, Roberto; Nigri, Giuseppe; Agnes, Salvatore; Manes, Gianpiero; D’Angelo, Francesco A.. - In: ONCO. - ISSN 2673-7523. - 44:5(2025), pp. 1-7. [10.3390/ onco5040044]
Association of TP53 Arg72Pro (rs1042522) Polymorphism with Pancreatic Cancer Risk in a Patient Cohort
Laura Antolino
;Stefania Scarpino;Gianluca Lopez;Paolo Aurello;Giuseppe Nigri;Francesco A. D’Angelo
2025
Abstract
Pancreatic cancer is one of the most deadly forms of cancer because it is often diagnosed too late, when treatments are less effective. Currently, there is no practical way to screen individuals who are at risk but have no symptoms. In this study, we describe a specific genetic variation in a gene called TP53, which is known to play a role in many types of cancer. We found that this variation appears to be more common in people with pancreatic cancer than in the general population. This suggests that individuals carrying this variation may have a higher risk of developing the disease. These findings may help open a new line of research aimed at identifying high-risk populations.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


