Unraveling the role of LncRNAs in glioblastoma progression: insights into signaling pathways and therapeutic potential
Glioblastoma (GBM) is one of the most aggressive types of brain cancer, characterized by its poor prognosis and low survival rate despite current treatment modalities. Because GBM is lethal, clarifying the pathogenesis’s underlying mechanisms is important, which are still poorly understood. Recent d...
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creator | Doghish, Ahmed S. Abd-Elmawla, Mai A. Hatawsh, Abdulrahman Zaki, Mohamed Bakr Aborehab, Nora M. Radwan, Abdullah F. Moussa, Rewan Eisa, Mahmoud A. Mageed, Sherif S. Abdel Mohammed, Osama A. Abdel-Reheim, Mustafa Ahmed Elimam, Hanan |
description | Glioblastoma (GBM) is one of the most aggressive types of brain cancer, characterized by its poor prognosis and low survival rate despite current treatment modalities. Because GBM is lethal, clarifying the pathogenesis’s underlying mechanisms is important, which are still poorly understood. Recent discoveries in the fields of molecular genetics and cancer biology have demonstrated the critical role that non-coding RNAs (ncRNAs), especially long non-coding RNAs (lncRNAs), play in the molecular pathophysiology of GBM growth. LncRNAs are transcripts longer than 200 nucleotides that do not encode proteins. They are significant epigenetic modulators that control gene e expression at several levels. Their dysregulation and interactions with important signaling pathways play a major role in the malignancy and development of GBM. The increasing role of lncRNAs in GBM pathogenesis is thoroughly examined in this review, with particular attention given to their regulation mechanisms in key signaling pathways such as PI3K/AKT, Wnt/β-catenin, and p53. It also looks into lncRNAs’ potential as new biomarkers and treatment targets for GBM. In addition, the study discusses the difficulties in delivering lncRNA-based medicines across the blood-brain barrier and identifies areas that need more research to advance lncRNA-oriented treatments for this deadly cancer.
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doi_str_mv | 10.1007/s11011-024-01456-y |
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Graphical abstract</description><subject>1-Phosphatidylinositol 3-kinase</subject><subject>AKT protein</subject><subject>Animals</subject><subject>Biochemistry</subject><subject>Biomarkers</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Blood-brain barrier</subject><subject>Brain Neoplasms - drug therapy</subject><subject>Brain Neoplasms - genetics</subject><subject>Brain Neoplasms - metabolism</subject><subject>Brain Neoplasms - therapy</subject><subject>Cancer</subject><subject>Disease Progression</subject><subject>Epigenetics</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Genetics</subject><subject>Glioblastoma</subject><subject>Glioblastoma - drug therapy</subject><subject>Glioblastoma - genetics</subject><subject>Glioblastoma - metabolism</subject><subject>Glioblastoma - therapy</subject><subject>Glioma</subject><subject>Humans</subject><subject>Malignancy</subject><subject>Medical prognosis</subject><subject>Metabolic Diseases</subject><subject>Neurology</subject><subject>Neurosciences</subject><subject>Non-coding RNA</subject><subject>Nucleotides</subject><subject>Oncology</subject><subject>p53 Protein</subject><subject>Pathogenesis</subject><subject>Review</subject><subject>RNA, Long Noncoding - genetics</subject><subject>RNA, Long Noncoding - metabolism</subject><subject>Signal Transduction</subject><subject>Wnt protein</subject><subject>β-Catenin</subject><issn>1573-7365</issn><issn>0885-7490</issn><issn>1573-7365</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUtP3DAUha0KVB7tH-gCWWLTTcCOH0m6Q4jSSiOQEKwtx7nJGGXsYDuD5t_jmaEPddGNfaX7nWPfexD6QskFJaS6jJQSSgtS8oJQLmSx-YCOqahYUTEpDv6qj9BJjM-EECZo8xEdsUbUjWjqY7R-ckGvYbRuwGkJOPgRsO_xwpmHu6uIrcPDaH076pj8SuMp-CFAjNa7b7kZ7bBMWyp5nGund0aTTstXvYlYu27rGvQEc7IGTz6BS1aPn9Bhr8cIn9_vU_T0_ebx-kexuL_9eX21KEwpZCqgY5STuhWC1ZryilMthBFc8EqWpBfMNB3LqwDZl21nKi0JcGZI22allMBO0de9b_73ywwxqZWNBsZRO_BzVIyysuZVPjN6_g_67OeQJ9pRjDS0ETJT5Z4ywccYoFdTsCsdNooStU1F7VNRORW1S0Vtsujs3XpuV9D9lvyKIQNsD8TccgOEP2__x_YN04CZgQ</recordid><startdate>20241126</startdate><enddate>20241126</enddate><creator>Doghish, Ahmed S.</creator><creator>Abd-Elmawla, Mai A.</creator><creator>Hatawsh, Abdulrahman</creator><creator>Zaki, Mohamed Bakr</creator><creator>Aborehab, Nora M.</creator><creator>Radwan, Abdullah F.</creator><creator>Moussa, Rewan</creator><creator>Eisa, Mahmoud A.</creator><creator>Mageed, Sherif S. Abdel</creator><creator>Mohammed, Osama A.</creator><creator>Abdel-Reheim, Mustafa Ahmed</creator><creator>Elimam, Hanan</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0136-7096</orcidid><orcidid>https://orcid.org/0000-0002-7728-0923</orcidid></search><sort><creationdate>20241126</creationdate><title>Unraveling the role of LncRNAs in glioblastoma progression: insights into signaling pathways and therapeutic potential</title><author>Doghish, Ahmed S. ; Abd-Elmawla, Mai A. ; Hatawsh, Abdulrahman ; Zaki, Mohamed Bakr ; Aborehab, Nora M. ; Radwan, Abdullah F. ; Moussa, Rewan ; Eisa, Mahmoud A. ; Mageed, Sherif S. Abdel ; Mohammed, Osama A. ; Abdel-Reheim, Mustafa Ahmed ; Elimam, Hanan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c256t-ed31408b5538a14741a55c54547620f53c9d3007e6f2bdc7a60e43c0bbed366e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>1-Phosphatidylinositol 3-kinase</topic><topic>AKT protein</topic><topic>Animals</topic><topic>Biochemistry</topic><topic>Biomarkers</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Blood-brain barrier</topic><topic>Brain Neoplasms - drug therapy</topic><topic>Brain Neoplasms - genetics</topic><topic>Brain Neoplasms - metabolism</topic><topic>Brain Neoplasms - therapy</topic><topic>Cancer</topic><topic>Disease Progression</topic><topic>Epigenetics</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Genetics</topic><topic>Glioblastoma</topic><topic>Glioblastoma - drug therapy</topic><topic>Glioblastoma - genetics</topic><topic>Glioblastoma - metabolism</topic><topic>Glioblastoma - therapy</topic><topic>Glioma</topic><topic>Humans</topic><topic>Malignancy</topic><topic>Medical prognosis</topic><topic>Metabolic Diseases</topic><topic>Neurology</topic><topic>Neurosciences</topic><topic>Non-coding RNA</topic><topic>Nucleotides</topic><topic>Oncology</topic><topic>p53 Protein</topic><topic>Pathogenesis</topic><topic>Review</topic><topic>RNA, Long Noncoding - genetics</topic><topic>RNA, Long Noncoding - metabolism</topic><topic>Signal Transduction</topic><topic>Wnt protein</topic><topic>β-Catenin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Doghish, Ahmed S.</creatorcontrib><creatorcontrib>Abd-Elmawla, Mai A.</creatorcontrib><creatorcontrib>Hatawsh, Abdulrahman</creatorcontrib><creatorcontrib>Zaki, Mohamed Bakr</creatorcontrib><creatorcontrib>Aborehab, Nora M.</creatorcontrib><creatorcontrib>Radwan, Abdullah F.</creatorcontrib><creatorcontrib>Moussa, Rewan</creatorcontrib><creatorcontrib>Eisa, Mahmoud A.</creatorcontrib><creatorcontrib>Mageed, Sherif S. Abdel</creatorcontrib><creatorcontrib>Mohammed, Osama A.</creatorcontrib><creatorcontrib>Abdel-Reheim, Mustafa Ahmed</creatorcontrib><creatorcontrib>Elimam, Hanan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Metabolic brain disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Doghish, Ahmed S.</au><au>Abd-Elmawla, Mai A.</au><au>Hatawsh, Abdulrahman</au><au>Zaki, Mohamed Bakr</au><au>Aborehab, Nora M.</au><au>Radwan, Abdullah F.</au><au>Moussa, Rewan</au><au>Eisa, Mahmoud A.</au><au>Mageed, Sherif S. Abdel</au><au>Mohammed, Osama A.</au><au>Abdel-Reheim, Mustafa Ahmed</au><au>Elimam, Hanan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Unraveling the role of LncRNAs in glioblastoma progression: insights into signaling pathways and therapeutic potential</atitle><jtitle>Metabolic brain disease</jtitle><stitle>Metab Brain Dis</stitle><addtitle>Metab Brain Dis</addtitle><date>2024-11-26</date><risdate>2024</risdate><volume>40</volume><issue>1</issue><spage>42</spage><pages>42-</pages><artnum>42</artnum><issn>1573-7365</issn><issn>0885-7490</issn><eissn>1573-7365</eissn><abstract>Glioblastoma (GBM) is one of the most aggressive types of brain cancer, characterized by its poor prognosis and low survival rate despite current treatment modalities. Because GBM is lethal, clarifying the pathogenesis’s underlying mechanisms is important, which are still poorly understood. Recent discoveries in the fields of molecular genetics and cancer biology have demonstrated the critical role that non-coding RNAs (ncRNAs), especially long non-coding RNAs (lncRNAs), play in the molecular pathophysiology of GBM growth. LncRNAs are transcripts longer than 200 nucleotides that do not encode proteins. They are significant epigenetic modulators that control gene e expression at several levels. Their dysregulation and interactions with important signaling pathways play a major role in the malignancy and development of GBM. The increasing role of lncRNAs in GBM pathogenesis is thoroughly examined in this review, with particular attention given to their regulation mechanisms in key signaling pathways such as PI3K/AKT, Wnt/β-catenin, and p53. It also looks into lncRNAs’ potential as new biomarkers and treatment targets for GBM. In addition, the study discusses the difficulties in delivering lncRNA-based medicines across the blood-brain barrier and identifies areas that need more research to advance lncRNA-oriented treatments for this deadly cancer.
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subjects | 1-Phosphatidylinositol 3-kinase AKT protein Animals Biochemistry Biomarkers Biomedical and Life Sciences Biomedicine Blood-brain barrier Brain Neoplasms - drug therapy Brain Neoplasms - genetics Brain Neoplasms - metabolism Brain Neoplasms - therapy Cancer Disease Progression Epigenetics Gene Expression Regulation, Neoplastic Genetics Glioblastoma Glioblastoma - drug therapy Glioblastoma - genetics Glioblastoma - metabolism Glioblastoma - therapy Glioma Humans Malignancy Medical prognosis Metabolic Diseases Neurology Neurosciences Non-coding RNA Nucleotides Oncology p53 Protein Pathogenesis Review RNA, Long Noncoding - genetics RNA, Long Noncoding - metabolism Signal Transduction Wnt protein β-Catenin |
title | Unraveling the role of LncRNAs in glioblastoma progression: insights into signaling pathways and therapeutic potential |
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