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Molecular Landscape of LncRNAs in Prostate Cancer: A focus on pathways and therapeutic targets for intervention

BACKGROUND: One of the most malignant tumors in men is prostate cancer that is still incurable due to its heterogenous and progressive natures. Genetic and epigenetic changes play significant roles in its development. The RNA molecules with more than 200 nucleotides in length are known as lncRNAs an...

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Autores principales: Mirzaei, Sepideh, Paskeh, Mahshid Deldar Abad, Okina, Elena, Gholami, Mohammad Hossein, Hushmandi, Kiavash, Hashemi, Mehrdad, Kalu, Azuma, Zarrabi, Ali, Nabavi, Noushin, Rabiee, Navid, Sharifi, Esmaeel, Karimi-Maleh, Hassan, Ashrafizadeh, Milad, Kumar, Alan Prem, Wang, Yuzhuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248128/
https://www.ncbi.nlm.nih.gov/pubmed/35773731
http://dx.doi.org/10.1186/s13046-022-02406-1
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author Mirzaei, Sepideh
Paskeh, Mahshid Deldar Abad
Okina, Elena
Gholami, Mohammad Hossein
Hushmandi, Kiavash
Hashemi, Mehrdad
Kalu, Azuma
Zarrabi, Ali
Nabavi, Noushin
Rabiee, Navid
Sharifi, Esmaeel
Karimi-Maleh, Hassan
Ashrafizadeh, Milad
Kumar, Alan Prem
Wang, Yuzhuo
author_facet Mirzaei, Sepideh
Paskeh, Mahshid Deldar Abad
Okina, Elena
Gholami, Mohammad Hossein
Hushmandi, Kiavash
Hashemi, Mehrdad
Kalu, Azuma
Zarrabi, Ali
Nabavi, Noushin
Rabiee, Navid
Sharifi, Esmaeel
Karimi-Maleh, Hassan
Ashrafizadeh, Milad
Kumar, Alan Prem
Wang, Yuzhuo
author_sort Mirzaei, Sepideh
collection PubMed
description BACKGROUND: One of the most malignant tumors in men is prostate cancer that is still incurable due to its heterogenous and progressive natures. Genetic and epigenetic changes play significant roles in its development. The RNA molecules with more than 200 nucleotides in length are known as lncRNAs and these epigenetic factors do not encode protein. They regulate gene expression at transcriptional, post-transcriptional and epigenetic levels. LncRNAs play vital biological functions in cells and in pathological events, hence their expression undergoes dysregulation. AIM OF REVIEW: The role of epigenetic alterations in prostate cancer development are emphasized here. Therefore, lncRNAs were chosen for this purpose and their expression level and interaction with other signaling networks in prostate cancer progression were examined. KEY SCIENTIFIC CONCEPTS OF REVIEW: The aberrant expression of lncRNAs in prostate cancer has been well-documented and progression rate of tumor cells are regulated via affecting STAT3, NF-κB, Wnt, PI3K/Akt and PTEN, among other molecular pathways. Furthermore, lncRNAs regulate radio-resistance and chemo-resistance features of prostate tumor cells. Overexpression of tumor-promoting lncRNAs such as HOXD-AS1 and CCAT1 can result in drug resistance. Besides, lncRNAs can induce immune evasion of prostate cancer via upregulating PD-1. Pharmacological compounds such as quercetin and curcumin have been applied for targeting lncRNAs. Furthermore, siRNA tool can reduce expression of lncRNAs thereby suppressing prostate cancer progression. Prognosis and diagnosis of prostate tumor at clinical course can be evaluated by lncRNAs. The expression level of exosomal lncRNAs such as lncRNA-p21 can be investigated in serum of prostate cancer patients as a reliable biomarker.
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spelling pubmed-92481282022-07-02 Molecular Landscape of LncRNAs in Prostate Cancer: A focus on pathways and therapeutic targets for intervention Mirzaei, Sepideh Paskeh, Mahshid Deldar Abad Okina, Elena Gholami, Mohammad Hossein Hushmandi, Kiavash Hashemi, Mehrdad Kalu, Azuma Zarrabi, Ali Nabavi, Noushin Rabiee, Navid Sharifi, Esmaeel Karimi-Maleh, Hassan Ashrafizadeh, Milad Kumar, Alan Prem Wang, Yuzhuo J Exp Clin Cancer Res Review BACKGROUND: One of the most malignant tumors in men is prostate cancer that is still incurable due to its heterogenous and progressive natures. Genetic and epigenetic changes play significant roles in its development. The RNA molecules with more than 200 nucleotides in length are known as lncRNAs and these epigenetic factors do not encode protein. They regulate gene expression at transcriptional, post-transcriptional and epigenetic levels. LncRNAs play vital biological functions in cells and in pathological events, hence their expression undergoes dysregulation. AIM OF REVIEW: The role of epigenetic alterations in prostate cancer development are emphasized here. Therefore, lncRNAs were chosen for this purpose and their expression level and interaction with other signaling networks in prostate cancer progression were examined. KEY SCIENTIFIC CONCEPTS OF REVIEW: The aberrant expression of lncRNAs in prostate cancer has been well-documented and progression rate of tumor cells are regulated via affecting STAT3, NF-κB, Wnt, PI3K/Akt and PTEN, among other molecular pathways. Furthermore, lncRNAs regulate radio-resistance and chemo-resistance features of prostate tumor cells. Overexpression of tumor-promoting lncRNAs such as HOXD-AS1 and CCAT1 can result in drug resistance. Besides, lncRNAs can induce immune evasion of prostate cancer via upregulating PD-1. Pharmacological compounds such as quercetin and curcumin have been applied for targeting lncRNAs. Furthermore, siRNA tool can reduce expression of lncRNAs thereby suppressing prostate cancer progression. Prognosis and diagnosis of prostate tumor at clinical course can be evaluated by lncRNAs. The expression level of exosomal lncRNAs such as lncRNA-p21 can be investigated in serum of prostate cancer patients as a reliable biomarker. BioMed Central 2022-07-01 /pmc/articles/PMC9248128/ /pubmed/35773731 http://dx.doi.org/10.1186/s13046-022-02406-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Mirzaei, Sepideh
Paskeh, Mahshid Deldar Abad
Okina, Elena
Gholami, Mohammad Hossein
Hushmandi, Kiavash
Hashemi, Mehrdad
Kalu, Azuma
Zarrabi, Ali
Nabavi, Noushin
Rabiee, Navid
Sharifi, Esmaeel
Karimi-Maleh, Hassan
Ashrafizadeh, Milad
Kumar, Alan Prem
Wang, Yuzhuo
Molecular Landscape of LncRNAs in Prostate Cancer: A focus on pathways and therapeutic targets for intervention
title Molecular Landscape of LncRNAs in Prostate Cancer: A focus on pathways and therapeutic targets for intervention
title_full Molecular Landscape of LncRNAs in Prostate Cancer: A focus on pathways and therapeutic targets for intervention
title_fullStr Molecular Landscape of LncRNAs in Prostate Cancer: A focus on pathways and therapeutic targets for intervention
title_full_unstemmed Molecular Landscape of LncRNAs in Prostate Cancer: A focus on pathways and therapeutic targets for intervention
title_short Molecular Landscape of LncRNAs in Prostate Cancer: A focus on pathways and therapeutic targets for intervention
title_sort molecular landscape of lncrnas in prostate cancer: a focus on pathways and therapeutic targets for intervention
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248128/
https://www.ncbi.nlm.nih.gov/pubmed/35773731
http://dx.doi.org/10.1186/s13046-022-02406-1
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