New insights into the interplay between long non‐coding RNAs and RNA‐binding proteins in cancer

With the development of proteomics and epigenetics, a large number of RNA‐binding proteins (RBPs) have been discovered in recent years, and the interaction between long non‐coding RNAs (lncRNAs) and RBPs has also received increasing attention. It is extremely important to conduct in‐depth research o...

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Published in:Cancer communications (London, England) Vol. 42; no. 2; pp. 117 - 140
Main Authors: Yao, Zi‐Ting, Yang, Yan‐Ming, Sun, Miao‐Miao, He, Yan, Liao, Long, Chen, Kui‐Sheng, Li, Bin
Format: Journal Article
Language:English
Published: United States John Wiley & Sons, Inc 01.02.2022
John Wiley and Sons Inc
Wiley
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ISSN:2523-3548, 2523-3548
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Abstract With the development of proteomics and epigenetics, a large number of RNA‐binding proteins (RBPs) have been discovered in recent years, and the interaction between long non‐coding RNAs (lncRNAs) and RBPs has also received increasing attention. It is extremely important to conduct in‐depth research on the lncRNA‐RBP interaction network, especially in the context of its role in the occurrence and development of cancer. Increasing evidence has demonstrated that lncRNA‐RBP interactions play a vital role in cancer progression; therefore, targeting these interactions could provide new insights for cancer drug discovery. In this review, we discussed how lncRNAs can interact with RBPs to regulate their localization, modification, stability, and activity and discussed the effects of RBPs on the stability, transport, transcription, and localization of lncRNAs. Moreover, we explored the regulation and influence of these interactions on lncRNAs, RBPs, and downstream pathways that are related to cancer development, such as N6‐methyladenosine (m6A) modification of lncRNAs. In addition, we discussed how the lncRNA‐RBP interaction network regulates cancer cell phenotypes, such as proliferation, apoptosis, metastasis, drug resistance, immunity, tumor environment, and metabolism. Furthermore, we summarized the therapeutic strategies that target the lncRNA‐RBP interaction network. Although these treatments are still in the experimental stage and various theories and processes are still being studied, we believe that these strategies may provide new ideas for cancer treatment.
AbstractList With the development of proteomics and epigenetics, a large number of RNA-binding proteins (RBPs) have been discovered in recent years, and the interaction between long non-coding RNAs (lncRNAs) and RBPs has also received increasing attention. It is extremely important to conduct in-depth research on the lncRNA-RBP interaction network, especially in the context of its role in the occurrence and development of cancer. Increasing evidence has demonstrated that lncRNA-RBP interactions play a vital role in cancer progression; therefore, targeting these interactions could provide new insights for cancer drug discovery. In this review, we discussed how lncRNAs can interact with RBPs to regulate their localization, modification, stability, and activity and discussed the effects of RBPs on the stability, transport, transcription, and localization of lncRNAs. Moreover, we explored the regulation and influence of these interactions on lncRNAs, RBPs, and downstream pathways that are related to cancer development, such as N6-methyladenosine (m6A) modification of lncRNAs. In addition, we discussed how the lncRNA-RBP interaction network regulates cancer cell phenotypes, such as proliferation, apoptosis, metastasis, drug resistance, immunity, tumor environment, and metabolism. Furthermore, we summarized the therapeutic strategies that target the lncRNA-RBP interaction network. Although these treatments are still in the experimental stage and various theories and processes are still being studied, we believe that these strategies may provide new ideas for cancer treatment.
With the development of proteomics and epigenetics, a large number of RNA-binding proteins (RBPs) have been discovered in recent years, and the interaction between long non-coding RNAs (lncRNAs) and RBPs has also received increasing attention. It is extremely important to conduct in-depth research on the lncRNA-RBP interaction network, especially in the context of its role in the occurrence and development of cancer. Increasing evidence has demonstrated that lncRNA-RBP interactions play a vital role in cancer progression; therefore, targeting these interactions could provide new insights for cancer drug discovery. In this review, we discussed how lncRNAs can interact with RBPs to regulate their localization, modification, stability, and activity and discussed the effects of RBPs on the stability, transport, transcription, and localization of lncRNAs. Moreover, we explored the regulation and influence of these interactions on lncRNAs, RBPs, and downstream pathways that are related to cancer development, such as N6-methyladenosine (m6A) modification of lncRNAs. In addition, we discussed how the lncRNA-RBP interaction network regulates cancer cell phenotypes, such as proliferation, apoptosis, metastasis, drug resistance, immunity, tumor environment, and metabolism. Furthermore, we summarized the therapeutic strategies that target the lncRNA-RBP interaction network. Although these treatments are still in the experimental stage and various theories and processes are still being studied, we believe that these strategies may provide new ideas for cancer treatment.With the development of proteomics and epigenetics, a large number of RNA-binding proteins (RBPs) have been discovered in recent years, and the interaction between long non-coding RNAs (lncRNAs) and RBPs has also received increasing attention. It is extremely important to conduct in-depth research on the lncRNA-RBP interaction network, especially in the context of its role in the occurrence and development of cancer. Increasing evidence has demonstrated that lncRNA-RBP interactions play a vital role in cancer progression; therefore, targeting these interactions could provide new insights for cancer drug discovery. In this review, we discussed how lncRNAs can interact with RBPs to regulate their localization, modification, stability, and activity and discussed the effects of RBPs on the stability, transport, transcription, and localization of lncRNAs. Moreover, we explored the regulation and influence of these interactions on lncRNAs, RBPs, and downstream pathways that are related to cancer development, such as N6-methyladenosine (m6A) modification of lncRNAs. In addition, we discussed how the lncRNA-RBP interaction network regulates cancer cell phenotypes, such as proliferation, apoptosis, metastasis, drug resistance, immunity, tumor environment, and metabolism. Furthermore, we summarized the therapeutic strategies that target the lncRNA-RBP interaction network. Although these treatments are still in the experimental stage and various theories and processes are still being studied, we believe that these strategies may provide new ideas for cancer treatment.
Abstract With the development of proteomics and epigenetics, a large number of RNA‐binding proteins (RBPs) have been discovered in recent years, and the interaction between long non‐coding RNAs (lncRNAs) and RBPs has also received increasing attention. It is extremely important to conduct in‐depth research on the lncRNA‐RBP interaction network, especially in the context of its role in the occurrence and development of cancer. Increasing evidence has demonstrated that lncRNA‐RBP interactions play a vital role in cancer progression; therefore, targeting these interactions could provide new insights for cancer drug discovery. In this review, we discussed how lncRNAs can interact with RBPs to regulate their localization, modification, stability, and activity and discussed the effects of RBPs on the stability, transport, transcription, and localization of lncRNAs. Moreover, we explored the regulation and influence of these interactions on lncRNAs, RBPs, and downstream pathways that are related to cancer development, such as N6‐methyladenosine (m6A) modification of lncRNAs. In addition, we discussed how the lncRNA‐RBP interaction network regulates cancer cell phenotypes, such as proliferation, apoptosis, metastasis, drug resistance, immunity, tumor environment, and metabolism. Furthermore, we summarized the therapeutic strategies that target the lncRNA‐RBP interaction network. Although these treatments are still in the experimental stage and various theories and processes are still being studied, we believe that these strategies may provide new ideas for cancer treatment.
Author Yang, Yan‐Ming
He, Yan
Chen, Kui‐Sheng
Li, Bin
Yao, Zi‐Ting
Sun, Miao‐Miao
Liao, Long
AuthorAffiliation 2 Department of Pathology Henan Key Laboratory of Tumor Pathology the First Affiliated Hospital of Zhengzhou University Zhengzhou Henan 450001 P. R. China
3 Ministry of Education Key Laboratory of Tumor Molecular Biology and Guangdong Provincial Key Laboratory of Bioengineering Medicine National Engineering Research Center of Genetic Medicine Institute of Biomedicine College of Life Science and Technology Jinan University Guangzhou Guangdong 510632 P. R. China
4 Key Laboratory of Biological Targeting Diagnosis Therapy and Rehabilitation of Guangdong Higher Education Institutes the Fifth Affiliated Hospital of Guangzhou Medical University Guangzhou Guangdong 510700 P. R. China
1 Ministry of Education Key Laboratory of Tumor Molecular Biology and Key Laboratory of Functional Protein Research of Guangdong Higher Education Institutes Institute of Life and Health Engineering Jinan University Guangzhou Guangdong 510632 P. R. China
AuthorAffiliation_xml – name: 2 Department of Pathology Henan Key Laboratory of Tumor Pathology the First Affiliated Hospital of Zhengzhou University Zhengzhou Henan 450001 P. R. China
– name: 3 Ministry of Education Key Laboratory of Tumor Molecular Biology and Guangdong Provincial Key Laboratory of Bioengineering Medicine National Engineering Research Center of Genetic Medicine Institute of Biomedicine College of Life Science and Technology Jinan University Guangzhou Guangdong 510632 P. R. China
– name: 4 Key Laboratory of Biological Targeting Diagnosis Therapy and Rehabilitation of Guangdong Higher Education Institutes the Fifth Affiliated Hospital of Guangzhou Medical University Guangzhou Guangdong 510700 P. R. China
– name: 1 Ministry of Education Key Laboratory of Tumor Molecular Biology and Key Laboratory of Functional Protein Research of Guangdong Higher Education Institutes Institute of Life and Health Engineering Jinan University Guangzhou Guangdong 510632 P. R. China
Author_xml – sequence: 1
  givenname: Zi‐Ting
  surname: Yao
  fullname: Yao, Zi‐Ting
  organization: Jinan University
– sequence: 2
  givenname: Yan‐Ming
  surname: Yang
  fullname: Yang, Yan‐Ming
  organization: Jinan University
– sequence: 3
  givenname: Miao‐Miao
  surname: Sun
  fullname: Sun, Miao‐Miao
  organization: the First Affiliated Hospital of Zhengzhou University
– sequence: 4
  givenname: Yan
  surname: He
  fullname: He, Yan
  organization: the Fifth Affiliated Hospital of Guangzhou Medical University
– sequence: 5
  givenname: Long
  surname: Liao
  fullname: Liao, Long
  organization: the Fifth Affiliated Hospital of Guangzhou Medical University
– sequence: 6
  givenname: Kui‐Sheng
  surname: Chen
  fullname: Chen, Kui‐Sheng
  email: chenksh2002@163.com
  organization: the First Affiliated Hospital of Zhengzhou University
– sequence: 7
  givenname: Bin
  orcidid: 0000-0002-8979-610X
  surname: Li
  fullname: Li, Bin
  email: lib2128@163.com
  organization: the Fifth Affiliated Hospital of Guangzhou Medical University
BackLink https://www.ncbi.nlm.nih.gov/pubmed/35019235$$D View this record in MEDLINE/PubMed
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Copyright 2022 The Authors. published by John Wiley & Sons Australia, Ltd. on behalf of Sun Yat‐sen University Cancer Center
2022 The Authors. Cancer Communications published by John Wiley & Sons Australia, Ltd. on behalf of Sun Yat-sen University Cancer Center.
2022. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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Issue 2
Keywords RNA-binding protein
interaction network
treatment strategy
cancer
long non-coding RNA
cancer epigenetics
lncRNA-RBP
Language English
License Attribution-NonCommercial-NoDerivs
2022 The Authors. Cancer Communications published by John Wiley & Sons Australia, Ltd. on behalf of Sun Yat-sen University Cancer Center.
This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
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Snippet With the development of proteomics and epigenetics, a large number of RNA‐binding proteins (RBPs) have been discovered in recent years, and the interaction...
With the development of proteomics and epigenetics, a large number of RNA-binding proteins (RBPs) have been discovered in recent years, and the interaction...
Abstract With the development of proteomics and epigenetics, a large number of RNA‐binding proteins (RBPs) have been discovered in recent years, and the...
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StartPage 117
SubjectTerms Binding sites
cancer
cancer epigenetics
Cell cycle
Cyclin-dependent kinases
Dehydrogenases
Epigenesis, Genetic
Epigenetics
Gene expression
Genomes
Growth factors
Humans
interaction network
Kinases
lncRNA‐RBP
long non‐coding RNA
Metastasis
MicroRNAs
Neoplasms - genetics
Neoplasms - metabolism
Prostate cancer
Proteins
Review
Reviews
RNA polymerase
RNA, Long Noncoding - genetics
RNA, Long Noncoding - metabolism
RNA-Binding Proteins - genetics
RNA-Binding Proteins - metabolism
RNA‐binding protein
Signal transduction
Stem cells
treatment strategy
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Title New insights into the interplay between long non‐coding RNAs and RNA‐binding proteins in cancer
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