Nanoconjugated long non-coding RNA MEG3 as a new therapeutic approach for Hepatocellular carcinoma

Background: Hepatocellular carcinoma (HCC) is an aggressive human cancer with a poor prognosis. Long non-coding RNAs (lncRNA) have multiple functions: epigenomic regulation, gene transcription, protein-coding gene translation, and genome defense. The involvement of lncRNAs in therapy offers a vast s...

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Main Authors: Mohamed Elzallat, Marwa Hassan, Nabila Elkramani, Tarek Aboushousha, Ahmed AbdelLatif, Noha Helal, Hoda Abu-Taleb, Eman El-Ahwany
Format: Article
Language:English
Published: Elsevier 2023-04-01
Series:Heliyon
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844023024957
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author Mohamed Elzallat
Marwa Hassan
Nabila Elkramani
Tarek Aboushousha
Ahmed AbdelLatif
Noha Helal
Hoda Abu-Taleb
Eman El-Ahwany
author_facet Mohamed Elzallat
Marwa Hassan
Nabila Elkramani
Tarek Aboushousha
Ahmed AbdelLatif
Noha Helal
Hoda Abu-Taleb
Eman El-Ahwany
author_sort Mohamed Elzallat
collection DOAJ
description Background: Hepatocellular carcinoma (HCC) is an aggressive human cancer with a poor prognosis. Long non-coding RNAs (lncRNA) have multiple functions: epigenomic regulation, gene transcription, protein-coding gene translation, and genome defense. The involvement of lncRNAs in therapy offers a vast step in cancer treatment. Objective: In the current study, a novel therapeutic regimen using polymer nanoparticle-mediated delivery of lncRNA was designed to control the progression of hepatocarcinogenesis. Methods: One hundred mice were divided into 5 groups. The first group served as a normal-control group and was injected with saline, whereas the pathological-control group (the second group) was injected with N-Nitrosodiethylamine (DEN) weekly for 16 weeks. Group 3, Group 4, and Group 5 were injected intrahepatically with polymer nanoparticles (NPs) alone, lncRNA MEG3 alone, and conjugated NPs, respectively, once/week for four weeks starting on the 12th week after DEN injection. After 16 weeks, animals were euthanized, and liver specimens and blood samples were collected for pathological, molecular, and biochemical assessment. Results: Compared to the pathological-control group, nanoconjugates lncRNA MEG3 demonstrated a significant improvement in histopathology and tumour-associated biomarkers. Furthermore, the expression of the SENP1 and PCNA was downregulated. Conclusion: MEG3 conjugated nanoparticles can be considered a novel therapeutic regimen for HCC.
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spelling doaj.art-17190c9c869647c9a98ec66b93a9a53d2023-04-29T14:56:04ZengElsevierHeliyon2405-84402023-04-0194e15288Nanoconjugated long non-coding RNA MEG3 as a new therapeutic approach for Hepatocellular carcinomaMohamed Elzallat0Marwa Hassan1Nabila Elkramani2Tarek Aboushousha3Ahmed AbdelLatif4Noha Helal5Hoda Abu-Taleb6Eman El-Ahwany7Immunology Department, Theodor Bilharz Research Institute, Giza, Egypt; Corresponding author.Immunology Department, Theodor Bilharz Research Institute, Giza, EgyptBiotechnology Program and Biology Department, School of Science and Engineering, American University in Cairo, Cairo, EgyptPathology Department, Theodor Bilharz Research Institute, Giza, EgyptBiotechnology Program and Biology Department, School of Science and Engineering, American University in Cairo, Cairo, Egypt; Corresponding author.Pathology Department, Theodor Bilharz Research Institute, Giza, EgyptEnviromental Research Department, Theodor Bilharz Research Institute, Giza, EgyptImmunology Department, Theodor Bilharz Research Institute, Giza, EgyptBackground: Hepatocellular carcinoma (HCC) is an aggressive human cancer with a poor prognosis. Long non-coding RNAs (lncRNA) have multiple functions: epigenomic regulation, gene transcription, protein-coding gene translation, and genome defense. The involvement of lncRNAs in therapy offers a vast step in cancer treatment. Objective: In the current study, a novel therapeutic regimen using polymer nanoparticle-mediated delivery of lncRNA was designed to control the progression of hepatocarcinogenesis. Methods: One hundred mice were divided into 5 groups. The first group served as a normal-control group and was injected with saline, whereas the pathological-control group (the second group) was injected with N-Nitrosodiethylamine (DEN) weekly for 16 weeks. Group 3, Group 4, and Group 5 were injected intrahepatically with polymer nanoparticles (NPs) alone, lncRNA MEG3 alone, and conjugated NPs, respectively, once/week for four weeks starting on the 12th week after DEN injection. After 16 weeks, animals were euthanized, and liver specimens and blood samples were collected for pathological, molecular, and biochemical assessment. Results: Compared to the pathological-control group, nanoconjugates lncRNA MEG3 demonstrated a significant improvement in histopathology and tumour-associated biomarkers. Furthermore, the expression of the SENP1 and PCNA was downregulated. Conclusion: MEG3 conjugated nanoparticles can be considered a novel therapeutic regimen for HCC.http://www.sciencedirect.com/science/article/pii/S2405844023024957LncRNAsMEG3HCCTherapyPolymer nanoparticles
spellingShingle Mohamed Elzallat
Marwa Hassan
Nabila Elkramani
Tarek Aboushousha
Ahmed AbdelLatif
Noha Helal
Hoda Abu-Taleb
Eman El-Ahwany
Nanoconjugated long non-coding RNA MEG3 as a new therapeutic approach for Hepatocellular carcinoma
Heliyon
LncRNAs
MEG3
HCC
Therapy
Polymer nanoparticles
title Nanoconjugated long non-coding RNA MEG3 as a new therapeutic approach for Hepatocellular carcinoma
title_full Nanoconjugated long non-coding RNA MEG3 as a new therapeutic approach for Hepatocellular carcinoma
title_fullStr Nanoconjugated long non-coding RNA MEG3 as a new therapeutic approach for Hepatocellular carcinoma
title_full_unstemmed Nanoconjugated long non-coding RNA MEG3 as a new therapeutic approach for Hepatocellular carcinoma
title_short Nanoconjugated long non-coding RNA MEG3 as a new therapeutic approach for Hepatocellular carcinoma
title_sort nanoconjugated long non coding rna meg3 as a new therapeutic approach for hepatocellular carcinoma
topic LncRNAs
MEG3
HCC
Therapy
Polymer nanoparticles
url http://www.sciencedirect.com/science/article/pii/S2405844023024957
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