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Dyslipidemia in Chinese Pancreatic Cancer Patients: A Two-Center Retrospective Study

Background: Pancreatic cancer (PC) is one of the most aggressive and lethal malignancies in the world. High cholesterol intake may have a certain association with an elevated risk of PC, though dyslipidemia in PC patients has rarely been reported. In this study, we compared serum lipids levels betwe...

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Autores principales: Wang, Feiyang, Huang, Li, Zhang, Jinyan, Fan, Junwei, Wu, Heshui, Xu, Junming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317532/
https://www.ncbi.nlm.nih.gov/pubmed/34335950
http://dx.doi.org/10.7150/jca.60340
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author Wang, Feiyang
Huang, Li
Zhang, Jinyan
Fan, Junwei
Wu, Heshui
Xu, Junming
author_facet Wang, Feiyang
Huang, Li
Zhang, Jinyan
Fan, Junwei
Wu, Heshui
Xu, Junming
author_sort Wang, Feiyang
collection PubMed
description Background: Pancreatic cancer (PC) is one of the most aggressive and lethal malignancies in the world. High cholesterol intake may have a certain association with an elevated risk of PC, though dyslipidemia in PC patients has rarely been reported. In this study, we compared serum lipids levels between PC and non-PC tumor patients and assessed their prognostic value in PC. Methods: 271 patients treated at Wuhan Union Hospital from January 2012 to December 2016 and 204 individuals at Shanghai General Hospital from January 2018 to December 2019 were recruited. Their demographic parameters, laboratory data, pathological information, and clinical outcomes were extracted and analyzed. The mRNA expressions of related lipoprotein, low density lipoprotein receptor (LDLR) and high density lipoprotein binding protein (HDLBP), in PC tissues and paired noncancerous tissues and follow-up information were assessed based on the GEO database (GSE15471 and GSE62165) and TCGA database. Results: A total of 172 non-PC tumor patients and 260 PC patients were finally eligible for our analysis. PC patients exhibited higher levels of serum triglyceride, cholesterol, and low-density lipoprotein (LDL) and a lower serum high-density lipoprotein (HDL) level on admission versus the non-PC tumor group. In PC patients, LDLR mRNA expression was upregulated, and HDLBP mRNA expression was downregulated in cancerous tissues compared to these levels in paired noncancerous tissues. The survival analysis revealed that dyslipidemia had a non-significant association with a poor prognosis, but PC patients with a high LDLR level were at risk of poor survival. Conclusion: Dyslipidemia is detected in PC patients but has a non-significant relation to PC prognosis. However, LDLR may be a potential predictive marker for PC prognosis.
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spelling pubmed-83175322021-07-29 Dyslipidemia in Chinese Pancreatic Cancer Patients: A Two-Center Retrospective Study Wang, Feiyang Huang, Li Zhang, Jinyan Fan, Junwei Wu, Heshui Xu, Junming J Cancer Research Paper Background: Pancreatic cancer (PC) is one of the most aggressive and lethal malignancies in the world. High cholesterol intake may have a certain association with an elevated risk of PC, though dyslipidemia in PC patients has rarely been reported. In this study, we compared serum lipids levels between PC and non-PC tumor patients and assessed their prognostic value in PC. Methods: 271 patients treated at Wuhan Union Hospital from January 2012 to December 2016 and 204 individuals at Shanghai General Hospital from January 2018 to December 2019 were recruited. Their demographic parameters, laboratory data, pathological information, and clinical outcomes were extracted and analyzed. The mRNA expressions of related lipoprotein, low density lipoprotein receptor (LDLR) and high density lipoprotein binding protein (HDLBP), in PC tissues and paired noncancerous tissues and follow-up information were assessed based on the GEO database (GSE15471 and GSE62165) and TCGA database. Results: A total of 172 non-PC tumor patients and 260 PC patients were finally eligible for our analysis. PC patients exhibited higher levels of serum triglyceride, cholesterol, and low-density lipoprotein (LDL) and a lower serum high-density lipoprotein (HDL) level on admission versus the non-PC tumor group. In PC patients, LDLR mRNA expression was upregulated, and HDLBP mRNA expression was downregulated in cancerous tissues compared to these levels in paired noncancerous tissues. The survival analysis revealed that dyslipidemia had a non-significant association with a poor prognosis, but PC patients with a high LDLR level were at risk of poor survival. Conclusion: Dyslipidemia is detected in PC patients but has a non-significant relation to PC prognosis. However, LDLR may be a potential predictive marker for PC prognosis. Ivyspring International Publisher 2021-07-03 /pmc/articles/PMC8317532/ /pubmed/34335950 http://dx.doi.org/10.7150/jca.60340 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Wang, Feiyang
Huang, Li
Zhang, Jinyan
Fan, Junwei
Wu, Heshui
Xu, Junming
Dyslipidemia in Chinese Pancreatic Cancer Patients: A Two-Center Retrospective Study
title Dyslipidemia in Chinese Pancreatic Cancer Patients: A Two-Center Retrospective Study
title_full Dyslipidemia in Chinese Pancreatic Cancer Patients: A Two-Center Retrospective Study
title_fullStr Dyslipidemia in Chinese Pancreatic Cancer Patients: A Two-Center Retrospective Study
title_full_unstemmed Dyslipidemia in Chinese Pancreatic Cancer Patients: A Two-Center Retrospective Study
title_short Dyslipidemia in Chinese Pancreatic Cancer Patients: A Two-Center Retrospective Study
title_sort dyslipidemia in chinese pancreatic cancer patients: a two-center retrospective study
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317532/
https://www.ncbi.nlm.nih.gov/pubmed/34335950
http://dx.doi.org/10.7150/jca.60340
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