Pancreatic Cancer Genetics

Author(s):  
Juan Iovanna ◽  
Ezequiel Luis Calvo ◽  
Jean Charles Dagorn ◽  
Nelson Dusetti
Pancreatology ◽  
2001 ◽  
Vol 1 (6) ◽  
pp. 571-575 ◽  
Author(s):  
E. Efthimiou ◽  
T. Crnogorac-Jurcevic ◽  
N.R. Lemoine

2004 ◽  
Vol 18 (1) ◽  
pp. 17-21 ◽  
Author(s):  
Margaret Lilley ◽  
Dawna Gilchrist

OBJECTIVE:Pancreatic cancer is known to aggregate in some families and has been associated with a wide variety of cancer syndromes. The authors describe their experience with pancreatic cancer and the range of associated cancer syndromes.METHODS:The charts of all patients seen for concern of a hereditary cancer syndrome in the Cancer Genetics Clinic at the University of Alberta between 1995 and 2002 were reviewed.RESULTS:Forty families reported a personal or family history of pancreatic cancer in the context of a possible hereditary cancer syndrome. Three additional families reported a history of pancreatitis. Twenty-four (56%) of those families were suspected of having a hereditary breast and ovarian cancer syndrome. A further seven (16%) were suspected of having hereditary nonpolyposis colon cancer. Only three (7%) were believed to be at risk for a site-specific pancreatic cancer syndrome. Another three (7%) were suspicious for hereditary pancreatitis. The remaining family histories were suggestive of Li-Fraumeni syndrome, von Hippel-Lindau syndrome or a nonspecific cancer predisposition.CONCLUSIONS:With such a wide variety of hereditary cancer syndromes associated with pancreatic cancer, an accurate assessment of the family history is essential to determine the most appropriate cancer screening for at-risk family members and to guide any molecular testing that may be offered.


Cancers ◽  
2020 ◽  
Vol 12 (7) ◽  
pp. 1872 ◽  
Author(s):  
Li-Lian Gan ◽  
Ling-Wei Hii ◽  
Shew-Fung Wong ◽  
Chee-Onn Leong ◽  
Chun-Wai Mai

Pancreatic cancer ranks high among the causes of cancer-related mortality. The prognosis of this grim condition has not improved significantly over the past 50 years, despite advancement in imaging techniques, cancer genetics and treatment modalities. Due to the relative difficulty in the early detection of pancreatic tumors, as low as 20% of patients are eligible for potentially curative surgery; moreover, chemotherapy and radiotherapy (RT) do not confer a great benefit in the overall survival of the patients. Currently, emerging developments in immunotherapy have yet to bring a significant clinical advantage among pancreatic cancer patients. In fact, pancreatic tumor-driven immune evasion possesses one of the greatest challenges leading to immunotherapeutic resistance. Most of the immune escape pathways are innate, while poor priming of hosts’ immune response and immunoediting constitute the adaptive immunosuppressive machinery. In this review, we extensively discuss the pathway perturbations undermining the anti-tumor immunity specific to pancreatic cancer. We also explore feasible up-and-coming therapeutic strategies that may restore immunity and address therapeutic resistance, bringing hope to eliminate the status quo in pancreatic cancer prognosis.


2016 ◽  
Vol 12 (3) ◽  
pp. 314-325 ◽  
Author(s):  
Laufey T. Amundadottir

1999 ◽  
Vol 10 ◽  
pp. S4-S8 ◽  
Author(s):  
M. Goggins ◽  
S.E. Kern ◽  
J.A. Offerhaus ◽  
R.H. Hruban

2001 ◽  
Vol 120 (5) ◽  
pp. A162-A162
Author(s):  
A KUTUP ◽  
S HOSCH ◽  
S PAPE ◽  
P SCHEUNEMANN ◽  
W KNOEFEL ◽  
...  

2001 ◽  
Vol 120 (5) ◽  
pp. A610-A610
Author(s):  
D LEE ◽  
J LEE ◽  
S JEONG ◽  
K KWON ◽  
W CHOI ◽  
...  

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