2006
DOI: 10.1002/ijc.21986
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Differing molecular pathology of pancreatic adenocarcinoma in Egyptian and United States patients

Abstract: Variations in genetic mutations in pancreatic carcinoma between different populations have not been studied extensively, especially in developing countries where pancreatic cancer is rare. We studied the molecular pathology of 44 pancreatic carcinomas from patients residing in a heavily polluted region in the Nile River delta and compared the findings with tumors from 44 United States (US) patients. We evaluated K-ras mutations in codon 12, p53 mutations in exons 5-8, and Gadd45a mutations in exons 1 and 4. Ov… Show more

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Cited by 17 publications
(13 citation statements)
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“…The study questionnaire elicited the information of demographic, residential, occupational, lifestyle and medical histories as well as reproductive changes for female subjects. The questionnaire had been used in our previous studies on the epidemiology of cancer in Egypt [34][35][36]. Following the interviews, blood samples were taken from all study subjects.…”
Section: Study Design and Study Populationmentioning
confidence: 99%
“…The study questionnaire elicited the information of demographic, residential, occupational, lifestyle and medical histories as well as reproductive changes for female subjects. The questionnaire had been used in our previous studies on the epidemiology of cancer in Egypt [34][35][36]. Following the interviews, blood samples were taken from all study subjects.…”
Section: Study Design and Study Populationmentioning
confidence: 99%
“…For this reason, securing the quality of hen eggs is an important issue for Chronic exposure to POPs was found to interfere with the activity of endogenous hormones in humans, including T4, T3 and TSH (Langer, 2010). Some evidence suggests that OCPs might contribute to increase the risk of exocrine pancreatic cancer (Soliman et al, 2006). It is also worth mentioning that chronic exposure to OPIs contribute to produce developmental neurotoxicity (Colborn, 2006).…”
Section: Introductionmentioning
confidence: 99%
“…Oncogenic K-ras activation can result in a wide variety of effects, from activation of a senescence program to increased cell proliferation and inhibition of apoptosis, depending on the cellular and molecular context [1,[13][14][15][16][17]. In addition, evidence from molecular pathology and epidemiology suggests that wild-type and mutated K-ras PDA may develop through pathways involving different host-gene-environment interactions [2,17,18]. There is accumulating evidencemainly from mouse models of human PDA-that acinar cells may contribute to the development of PDA; this process may be particularly relevant for patients with chronic pancreatitis [13,14].…”
Section: Introductionmentioning
confidence: 99%