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A New Fusion Peptide Targeting Pancreatic Cancer and Inhibiting Tumor Growth

BACKGROUND: Pancreatic cancer is a highly malignant tumor of the digestive system. Early pancreatic cancer is often difficult to diagnosis due to its atypical clinical symptoms. Patients with pancreatic cancer have a very poor prognosis because they have lost the opportunity for radical surgical tum...

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Autores principales: Zheng, Lei, Zhang, Bo, He, Xiaoman, Cao, Guodong, Li, Yongzhou, Cai, Kailun, Yang, Bin, Wu, Yulian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7434629/
https://www.ncbi.nlm.nih.gov/pubmed/32884283
http://dx.doi.org/10.2147/OTT.S246969
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author Zheng, Lei
Zhang, Bo
He, Xiaoman
Cao, Guodong
Li, Yongzhou
Cai, Kailun
Yang, Bin
Wu, Yulian
author_facet Zheng, Lei
Zhang, Bo
He, Xiaoman
Cao, Guodong
Li, Yongzhou
Cai, Kailun
Yang, Bin
Wu, Yulian
author_sort Zheng, Lei
collection PubMed
description BACKGROUND: Pancreatic cancer is a highly malignant tumor of the digestive system. Early pancreatic cancer is often difficult to diagnosis due to its atypical clinical symptoms. Patients with pancreatic cancer have a very poor prognosis because they have lost the opportunity for radical surgical tumor resection and they are less sensitive to the clinically used radiotherapy and chemotherapy. METHODS: In this study, a peptide targeting pancreatic cancer cells was screened by phage display technology, and its targeting property was evaluated in vitro using PANC1 cells by fluorescence imaging and flow cytometry. Furthermore, the targeting peptide was conjugated to the pro-apoptotic KLAKLAKKLAKLAK (KLA), the fusion peptide and its targeting ability that allowing KLA to specifically enter pancreatic tumor cells in vitro and in vivo was confirmed by fluorescence imaging and in vivo imaging system (IVIS). Its mechanism was determined using flow cytometry, mitochondrial membrane potential evaluation and Western blot. The inhibitory effect on pancreatic tumor growth and toxic effects were evaluated by animal experiment. RESULTS: Due to the internalization facilitated by the targeting mechanism of the targeting peptide, KLA specifically entered pancreatic cancer cells, destroyed mitochondria and induced apoptosis. The fusion peptide and its targeting ability that allowing KLA to specifically enter pancreatic tumor cells and exert a significant inhibitory effect on pancreatic tumor growth with reduced toxic effects. CONCLUSION: This approach possesses potential advantages in the clinical diagnosis and treatment of pancreatic cancer.
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spelling pubmed-74346292020-09-02 A New Fusion Peptide Targeting Pancreatic Cancer and Inhibiting Tumor Growth Zheng, Lei Zhang, Bo He, Xiaoman Cao, Guodong Li, Yongzhou Cai, Kailun Yang, Bin Wu, Yulian Onco Targets Ther Original Research BACKGROUND: Pancreatic cancer is a highly malignant tumor of the digestive system. Early pancreatic cancer is often difficult to diagnosis due to its atypical clinical symptoms. Patients with pancreatic cancer have a very poor prognosis because they have lost the opportunity for radical surgical tumor resection and they are less sensitive to the clinically used radiotherapy and chemotherapy. METHODS: In this study, a peptide targeting pancreatic cancer cells was screened by phage display technology, and its targeting property was evaluated in vitro using PANC1 cells by fluorescence imaging and flow cytometry. Furthermore, the targeting peptide was conjugated to the pro-apoptotic KLAKLAKKLAKLAK (KLA), the fusion peptide and its targeting ability that allowing KLA to specifically enter pancreatic tumor cells in vitro and in vivo was confirmed by fluorescence imaging and in vivo imaging system (IVIS). Its mechanism was determined using flow cytometry, mitochondrial membrane potential evaluation and Western blot. The inhibitory effect on pancreatic tumor growth and toxic effects were evaluated by animal experiment. RESULTS: Due to the internalization facilitated by the targeting mechanism of the targeting peptide, KLA specifically entered pancreatic cancer cells, destroyed mitochondria and induced apoptosis. The fusion peptide and its targeting ability that allowing KLA to specifically enter pancreatic tumor cells and exert a significant inhibitory effect on pancreatic tumor growth with reduced toxic effects. CONCLUSION: This approach possesses potential advantages in the clinical diagnosis and treatment of pancreatic cancer. Dove 2020-08-12 /pmc/articles/PMC7434629/ /pubmed/32884283 http://dx.doi.org/10.2147/OTT.S246969 Text en © 2020 Zheng et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Zheng, Lei
Zhang, Bo
He, Xiaoman
Cao, Guodong
Li, Yongzhou
Cai, Kailun
Yang, Bin
Wu, Yulian
A New Fusion Peptide Targeting Pancreatic Cancer and Inhibiting Tumor Growth
title A New Fusion Peptide Targeting Pancreatic Cancer and Inhibiting Tumor Growth
title_full A New Fusion Peptide Targeting Pancreatic Cancer and Inhibiting Tumor Growth
title_fullStr A New Fusion Peptide Targeting Pancreatic Cancer and Inhibiting Tumor Growth
title_full_unstemmed A New Fusion Peptide Targeting Pancreatic Cancer and Inhibiting Tumor Growth
title_short A New Fusion Peptide Targeting Pancreatic Cancer and Inhibiting Tumor Growth
title_sort new fusion peptide targeting pancreatic cancer and inhibiting tumor growth
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7434629/
https://www.ncbi.nlm.nih.gov/pubmed/32884283
http://dx.doi.org/10.2147/OTT.S246969
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