Exploring the lncRNA-VEGF axis: Implications for cancer detection and therapy
Cancer is a complicated illness that spreads indefinitely owing to epigenetic, genetic, and genomic alterations. Cancer cell multidrug susceptibility represents a severe barrier in cancer therapy. As a result, creating effective therapies requires a better knowledge of the mechanisms driving cancer...
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creator | Alharthi, Nahed S. Al-Zahrani, Maryam Hassan Hazazi, Ali Alhuthali, Hayaa Moeed Gharib, Amal F. alzahrani, Shatha Altalhi, Wafa Almalki, Waleed Hassan Khan, Farhan R. |
description | Cancer is a complicated illness that spreads indefinitely owing to epigenetic, genetic, and genomic alterations. Cancer cell multidrug susceptibility represents a severe barrier in cancer therapy. As a result, creating effective therapies requires a better knowledge of the mechanisms driving cancer development, progress, and resistance to medications. The human genome is predominantly made up of long non coding RNAs (lncRNAs), which are currently identified as critical moderators in a variety of biological functions. Recent research has found that changes in lncRNAs are closely related to cancer biology. The vascular endothelial growth factor (VEGF) signalling system is necessary for angiogenesis and vascular growth and has been related to an array of health illnesses, such as cancer. LncRNAs have been identified to alter a variety of cancer-related processes, notably the division of cells, movement, angiogenesis, and treatment sensitivity. Furthermore, lncRNAs may modulate immune suppression and are being investigated as possible indicators for early identification of cancer. Various lncRNAs have been associated with cancer development and advancement, serving as cancer-causing or suppressing genes. Several lncRNAs have been demonstrated through research to impact the VEGF cascade, resulting in changes in angiogenesis and tumor severity. For example, the lncRNA nuclear paraspeckle assembly transcript 1 (NEAT1) has been shown to foster the formation of oral squamous cell carcinoma and the epithelial-mesenchymal transition by stimulating the VEGF-A and Notch systems. Plasmacytoma variant translocation 1 (PVT1) promotes angiogenesis in non-small-cell lung cancer by affecting miR-29c and boosting the VEGF cascade. Furthermore, lncRNAs regulate VEGF production and angiogenesis by interacting with multiple downstream signalling networks, including Wnt, p53, and AKT systems. Identifying how lncRNAs engage with the VEGF cascade in cancer gives beneficial insights into tumor biology and possible treatment strategies. Exploring the complicated interaction between lncRNAs and the VEGF pathway certainly paves avenues for novel ways to detect better accurately, prognosis, and cure cancers. Future studies in this area could open avenues toward the creation of innovative cancer therapy regimens that enhance the lives of patients. |
doi_str_mv | 10.1016/j.prp.2023.154998 |
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Cancer cell multidrug susceptibility represents a severe barrier in cancer therapy. As a result, creating effective therapies requires a better knowledge of the mechanisms driving cancer development, progress, and resistance to medications. The human genome is predominantly made up of long non coding RNAs (lncRNAs), which are currently identified as critical moderators in a variety of biological functions. Recent research has found that changes in lncRNAs are closely related to cancer biology. The vascular endothelial growth factor (VEGF) signalling system is necessary for angiogenesis and vascular growth and has been related to an array of health illnesses, such as cancer. LncRNAs have been identified to alter a variety of cancer-related processes, notably the division of cells, movement, angiogenesis, and treatment sensitivity. Furthermore, lncRNAs may modulate immune suppression and are being investigated as possible indicators for early identification of cancer. Various lncRNAs have been associated with cancer development and advancement, serving as cancer-causing or suppressing genes. Several lncRNAs have been demonstrated through research to impact the VEGF cascade, resulting in changes in angiogenesis and tumor severity. For example, the lncRNA nuclear paraspeckle assembly transcript 1 (NEAT1) has been shown to foster the formation of oral squamous cell carcinoma and the epithelial-mesenchymal transition by stimulating the VEGF-A and Notch systems. Plasmacytoma variant translocation 1 (PVT1) promotes angiogenesis in non-small-cell lung cancer by affecting miR-29c and boosting the VEGF cascade. Furthermore, lncRNAs regulate VEGF production and angiogenesis by interacting with multiple downstream signalling networks, including Wnt, p53, and AKT systems. Identifying how lncRNAs engage with the VEGF cascade in cancer gives beneficial insights into tumor biology and possible treatment strategies. Exploring the complicated interaction between lncRNAs and the VEGF pathway certainly paves avenues for novel ways to detect better accurately, prognosis, and cure cancers. Future studies in this area could open avenues toward the creation of innovative cancer therapy regimens that enhance the lives of patients.</description><identifier>ISSN: 0344-0338</identifier><identifier>EISSN: 1618-0631</identifier><identifier>DOI: 10.1016/j.prp.2023.154998</identifier><identifier>PMID: 38056133</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>Cancer ; LncRNA ; Non-small-cell lung cancer ; PVT1 ; VEGF</subject><ispartof>Pathology, research and practice, 2024-01, Vol.253, p.154998-154998, Article 154998</ispartof><rights>2023 Elsevier GmbH</rights><rights>Copyright © 2023 Elsevier GmbH. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c305t-585d928af1fea85105025bf833197b62d95707c4134e38193fb51ad9b04ce30c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.prp.2023.154998$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27907,27908,45978</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38056133$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alharthi, Nahed S.</creatorcontrib><creatorcontrib>Al-Zahrani, Maryam Hassan</creatorcontrib><creatorcontrib>Hazazi, Ali</creatorcontrib><creatorcontrib>Alhuthali, Hayaa Moeed</creatorcontrib><creatorcontrib>Gharib, Amal F.</creatorcontrib><creatorcontrib>alzahrani, Shatha</creatorcontrib><creatorcontrib>Altalhi, Wafa</creatorcontrib><creatorcontrib>Almalki, Waleed Hassan</creatorcontrib><creatorcontrib>Khan, Farhan R.</creatorcontrib><title>Exploring the lncRNA-VEGF axis: Implications for cancer detection and therapy</title><title>Pathology, research and practice</title><addtitle>Pathol Res Pract</addtitle><description>Cancer is a complicated illness that spreads indefinitely owing to epigenetic, genetic, and genomic alterations. Cancer cell multidrug susceptibility represents a severe barrier in cancer therapy. As a result, creating effective therapies requires a better knowledge of the mechanisms driving cancer development, progress, and resistance to medications. The human genome is predominantly made up of long non coding RNAs (lncRNAs), which are currently identified as critical moderators in a variety of biological functions. Recent research has found that changes in lncRNAs are closely related to cancer biology. The vascular endothelial growth factor (VEGF) signalling system is necessary for angiogenesis and vascular growth and has been related to an array of health illnesses, such as cancer. LncRNAs have been identified to alter a variety of cancer-related processes, notably the division of cells, movement, angiogenesis, and treatment sensitivity. Furthermore, lncRNAs may modulate immune suppression and are being investigated as possible indicators for early identification of cancer. Various lncRNAs have been associated with cancer development and advancement, serving as cancer-causing or suppressing genes. Several lncRNAs have been demonstrated through research to impact the VEGF cascade, resulting in changes in angiogenesis and tumor severity. For example, the lncRNA nuclear paraspeckle assembly transcript 1 (NEAT1) has been shown to foster the formation of oral squamous cell carcinoma and the epithelial-mesenchymal transition by stimulating the VEGF-A and Notch systems. Plasmacytoma variant translocation 1 (PVT1) promotes angiogenesis in non-small-cell lung cancer by affecting miR-29c and boosting the VEGF cascade. Furthermore, lncRNAs regulate VEGF production and angiogenesis by interacting with multiple downstream signalling networks, including Wnt, p53, and AKT systems. Identifying how lncRNAs engage with the VEGF cascade in cancer gives beneficial insights into tumor biology and possible treatment strategies. Exploring the complicated interaction between lncRNAs and the VEGF pathway certainly paves avenues for novel ways to detect better accurately, prognosis, and cure cancers. Future studies in this area could open avenues toward the creation of innovative cancer therapy regimens that enhance the lives of patients.</description><subject>Cancer</subject><subject>LncRNA</subject><subject>Non-small-cell lung cancer</subject><subject>PVT1</subject><subject>VEGF</subject><issn>0344-0338</issn><issn>1618-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kE1Lw0AURQdRtH78ADeSpZvU9_IyyYyuilQtVAVRt8NkMtEpaRJnUtF_b0qrS1cPLudeeIexU4QxAmYXi3Hnu3ECCY2Rp1KKHTbCDEUMGeEuGwGlaQxE4oAdhrAAgBxS3GcHJIBnSDRi99Ovrm69a96i_t1GdWOeHibx6_T2JtJfLlxGs2VXO6N71zYhqlofGd0Y66PS9tas00g35brrdfd9zPYqXQd7sr1H7OVm-nx9F88fb2fXk3lsCHgfc8FLmQhdYWW14AgcEl5UgghlXmRJKXkOuUmRUksCJVUFR13KAlJjCQwdsfPNbufbj5UNvVq6YGxd68a2q6ASISXliFIMKG5Q49sQvK1U591S-2-FoNYW1WJIOrW2qDYWh87Zdn5VLG351_jVNgBXG8AOT34661Uwzg5eSucHK6ps3T_zPzajgMY</recordid><startdate>202401</startdate><enddate>202401</enddate><creator>Alharthi, Nahed S.</creator><creator>Al-Zahrani, Maryam Hassan</creator><creator>Hazazi, Ali</creator><creator>Alhuthali, Hayaa Moeed</creator><creator>Gharib, Amal F.</creator><creator>alzahrani, Shatha</creator><creator>Altalhi, Wafa</creator><creator>Almalki, Waleed Hassan</creator><creator>Khan, Farhan R.</creator><general>Elsevier GmbH</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202401</creationdate><title>Exploring the lncRNA-VEGF axis: Implications for cancer detection and therapy</title><author>Alharthi, Nahed S. ; Al-Zahrani, Maryam Hassan ; Hazazi, Ali ; Alhuthali, Hayaa Moeed ; Gharib, Amal F. ; alzahrani, Shatha ; Altalhi, Wafa ; Almalki, Waleed Hassan ; Khan, Farhan R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c305t-585d928af1fea85105025bf833197b62d95707c4134e38193fb51ad9b04ce30c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Cancer</topic><topic>LncRNA</topic><topic>Non-small-cell lung cancer</topic><topic>PVT1</topic><topic>VEGF</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alharthi, Nahed S.</creatorcontrib><creatorcontrib>Al-Zahrani, Maryam Hassan</creatorcontrib><creatorcontrib>Hazazi, Ali</creatorcontrib><creatorcontrib>Alhuthali, Hayaa Moeed</creatorcontrib><creatorcontrib>Gharib, Amal F.</creatorcontrib><creatorcontrib>alzahrani, Shatha</creatorcontrib><creatorcontrib>Altalhi, Wafa</creatorcontrib><creatorcontrib>Almalki, Waleed Hassan</creatorcontrib><creatorcontrib>Khan, Farhan R.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Pathology, research and practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alharthi, Nahed S.</au><au>Al-Zahrani, Maryam Hassan</au><au>Hazazi, Ali</au><au>Alhuthali, Hayaa Moeed</au><au>Gharib, Amal F.</au><au>alzahrani, Shatha</au><au>Altalhi, Wafa</au><au>Almalki, Waleed Hassan</au><au>Khan, Farhan R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exploring the lncRNA-VEGF axis: Implications for cancer detection and therapy</atitle><jtitle>Pathology, research and practice</jtitle><addtitle>Pathol Res Pract</addtitle><date>2024-01</date><risdate>2024</risdate><volume>253</volume><spage>154998</spage><epage>154998</epage><pages>154998-154998</pages><artnum>154998</artnum><issn>0344-0338</issn><eissn>1618-0631</eissn><abstract>Cancer is a complicated illness that spreads indefinitely owing to epigenetic, genetic, and genomic alterations. Cancer cell multidrug susceptibility represents a severe barrier in cancer therapy. As a result, creating effective therapies requires a better knowledge of the mechanisms driving cancer development, progress, and resistance to medications. The human genome is predominantly made up of long non coding RNAs (lncRNAs), which are currently identified as critical moderators in a variety of biological functions. Recent research has found that changes in lncRNAs are closely related to cancer biology. The vascular endothelial growth factor (VEGF) signalling system is necessary for angiogenesis and vascular growth and has been related to an array of health illnesses, such as cancer. LncRNAs have been identified to alter a variety of cancer-related processes, notably the division of cells, movement, angiogenesis, and treatment sensitivity. Furthermore, lncRNAs may modulate immune suppression and are being investigated as possible indicators for early identification of cancer. Various lncRNAs have been associated with cancer development and advancement, serving as cancer-causing or suppressing genes. Several lncRNAs have been demonstrated through research to impact the VEGF cascade, resulting in changes in angiogenesis and tumor severity. For example, the lncRNA nuclear paraspeckle assembly transcript 1 (NEAT1) has been shown to foster the formation of oral squamous cell carcinoma and the epithelial-mesenchymal transition by stimulating the VEGF-A and Notch systems. Plasmacytoma variant translocation 1 (PVT1) promotes angiogenesis in non-small-cell lung cancer by affecting miR-29c and boosting the VEGF cascade. Furthermore, lncRNAs regulate VEGF production and angiogenesis by interacting with multiple downstream signalling networks, including Wnt, p53, and AKT systems. Identifying how lncRNAs engage with the VEGF cascade in cancer gives beneficial insights into tumor biology and possible treatment strategies. Exploring the complicated interaction between lncRNAs and the VEGF pathway certainly paves avenues for novel ways to detect better accurately, prognosis, and cure cancers. Future studies in this area could open avenues toward the creation of innovative cancer therapy regimens that enhance the lives of patients.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>38056133</pmid><doi>10.1016/j.prp.2023.154998</doi><tpages>1</tpages></addata></record> |
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subjects | Cancer LncRNA Non-small-cell lung cancer PVT1 VEGF |
title | Exploring the lncRNA-VEGF axis: Implications for cancer detection and therapy |
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