Cell Membrane Fatty Acids and PIPs Modulate the Etiology of Pancreatic Cancer by Regulating AKT

Pancreatic ductal adenocarcinoma (PDAC) is one of the worst solid malignancies in regard to outcomes and metabolic dysfunction leading to cachexia. It is alarming that PDAC incidence rates continue to increase and warrant the need for innovative approaches to combat this disease. Due to its relative...

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Veröffentlicht in:Nutrients 2025-01, Vol.17 (1), p.150
Hauptverfasser: Torres, Carolina, Mancinelli, Georgina, Chen, Jee-Wei Emily, Cordoba-Chacon, Jose, Pins, Danielle, Saeed, Sara, McKinney, Ronald, Castellanos, Karla, Orsi, Giulia, Singhal, Megha, Patel, Akshar, Acebedo, Jose, Coleman, Adonis, Heneche, Jorge, Yalagala, Poorna Chandra Rao, Subbaiah, Papasani V, Leal, Cecilia, Grimaldo, Sam, Ortuno, Francisco M, Bishehsari, Faraz, Grippo, Paul J
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container_issue 1
container_start_page 150
container_title Nutrients
container_volume 17
creator Torres, Carolina
Mancinelli, Georgina
Chen, Jee-Wei Emily
Cordoba-Chacon, Jose
Pins, Danielle
Saeed, Sara
McKinney, Ronald
Castellanos, Karla
Orsi, Giulia
Singhal, Megha
Patel, Akshar
Acebedo, Jose
Coleman, Adonis
Heneche, Jorge
Yalagala, Poorna Chandra Rao
Subbaiah, Papasani V
Leal, Cecilia
Grimaldo, Sam
Ortuno, Francisco M
Bishehsari, Faraz
Grippo, Paul J
description Pancreatic ductal adenocarcinoma (PDAC) is one of the worst solid malignancies in regard to outcomes and metabolic dysfunction leading to cachexia. It is alarming that PDAC incidence rates continue to increase and warrant the need for innovative approaches to combat this disease. Due to its relatively slow progression (10-20 years), prevention strategies represent an effective means to improve outcomes. One of the risk factors for many cancers and for pancreatic cancer in particular is diet. Hence, our objective is to understand how a diet rich in ω3 and ω6 polyunsaturated fatty acids affects the progression of this disease. We investigated polyunsaturated fatty acid (PUFA) effects on disease progression employing both (PDAC cell lines) and (EL-Kras and KC mice) approaches. Also, we gathered data from the National Health and Nutrition Examination Survey (NHANES) and the National Cancer Institute (NCI) from 1999 to 2017 for a retrospective observational study. The consumption of PUFAs in a patient population correlates with increased PDAC incidence, particularly when the ω3 intake increases to a lesser extent than ω6. Our data demonstrate dietary PUFAs can be incorporated into plasma membrane lipids affecting PI3K/AKT signaling and support the emergence of membrane-targeted therapies. Moreover, we show that the phospholipid composition of a lipid nanoparticle (LNP) can impact the cell membrane integrity and, ultimately, cell viability after administration of these LNPs. Cancer prevention is impactful particularly for those with very poor prognosis, including pancreatic cancer. Our results point to the importance of dietary intervention in this disease when detected early and the potential to improve the antiproliferative effect of drug efficacy when combined with these regimens in later stages of pancreatic cancer.
doi_str_mv 10.3390/nu17010150
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source MDPI - Multidisciplinary Digital Publishing Institute; MEDLINE; PubMed Central; EZB Electronic Journals Library; PubMed Central Open Access
subjects Animals
Aprotinin
Cancer
Carcinoma, Pancreatic Ductal
Cell Line, Tumor
Cell Membrane - metabolism
Cell membranes
Diet
Fatty acids
Fatty Acids - metabolism
Fatty Acids, Omega-3 - pharmacology
Fatty Acids, Omega-6 - administration & dosage
Fatty Acids, Omega-6 - pharmacology
FDA approval
Health aspects
Health surveys
Humans
Lipids
Membrane lipids
Membranes
Mice
Nanoparticles
Nutrition research
Observational studies
Oncology, Experimental
Ostomy
Pancreatic cancer
Pancreatic Neoplasms
Penicillin G
Phosphorylation
Physiology
Prevention
Proteins
Proto-Oncogene Proteins c-akt - metabolism
Retrospective Studies
Signal Transduction
Unsaturated fatty acids
title Cell Membrane Fatty Acids and PIPs Modulate the Etiology of Pancreatic Cancer by Regulating AKT
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