Long noncoding RNA (lncRNA) H19: An essential developmental regulator with expanding roles in cancer, stem cell differentiation, and metabolic diseases

Recent advances in deep sequencing technologies have revealed that, while less than 2% of the human genome is transcribed into mRNA for protein synthesis, over 80% of the genome is transcribed, leading to the production of large amounts of noncoding RNAs (ncRNAs). It has been shown that ncRNAs, espe...

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Published in:Genes & diseases Vol. 10; no. 4; pp. 1351 - 1366
Main Authors: Liao, Junyi, Chen, Bowen, Zhu, Zhenglin, Du, Chengcheng, Gao, Shengqiang, Zhao, Guozhi, Zhao, Piao, Wang, Yonghui, Wang, Annie, Schwartz, Zander, Song, Lily, Hong, Jeffrey, Wagstaff, William, Haydon, Rex C., Luu, Hue H., Fan, Jiaming, Reid, Russell R., He, Tong-Chuan, Shi, Lewis, Hu, Ning, Huang, Wei
Format: Journal Article
Language:English
Published: Netherlands Elsevier B.V 01.07.2023
Chongqing Medical University
KeAi Communications Co., Ltd
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ISSN:2352-3042, 2352-4820, 2352-3042
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Abstract Recent advances in deep sequencing technologies have revealed that, while less than 2% of the human genome is transcribed into mRNA for protein synthesis, over 80% of the genome is transcribed, leading to the production of large amounts of noncoding RNAs (ncRNAs). It has been shown that ncRNAs, especially long non-coding RNAs (lncRNAs), may play crucial regulatory roles in gene expression. As one of the first isolated and reported lncRNAs, H19 has gained much attention due to its essential roles in regulating many physiological and/or pathological processes including embryogenesis, development, tumorigenesis, osteogenesis, and metabolism. Mechanistically, H19 mediates diverse regulatory functions by serving as competing endogenous RNAs (CeRNAs), Igf2/H19 imprinted tandem gene, modular scaffold, cooperating with H19 antisense, and acting directly with other mRNAs or lncRNAs. Here, we summarized the current understanding of H19 in embryogenesis and development, cancer development and progression, mesenchymal stem cell lineage-specific differentiation, and metabolic diseases. We discussed the potential regulatory mechanisms underlying H19's functions in those processes although more in-depth studies are warranted to delineate the exact molecular, cellular, epigenetic, and genomic regulatory mechanisms underlying the physiological and pathological roles of H19. Ultimately, these lines of investigation may lead to the development of novel therapeutics for human diseases by exploiting H19 functions.
AbstractList Recent advances in deep sequencing technologies have revealed that, while less than 2% of the human genome is transcribed into mRNA for protein synthesis, over 80% of the genome is transcribed, leading to the production of large amounts of noncoding RNAs (ncRNAs). It has been shown that ncRNAs, especially long non-coding RNAs (lncRNAs), may play crucial regulatory roles in gene expression. As one of the first isolated and reported lncRNAs, H19 has gained much attention due to its essential roles in regulating many physiological and/or pathological processes including embryogenesis, development, tumorigenesis, osteogenesis, and metabolism. Mechanistically, H19 mediates diverse regulatory functions by serving as competing endogenous RNAs (CeRNAs), Igf2/H19 imprinted tandem gene, modular scaffold, cooperating with H19 antisense, and acting directly with other mRNAs or lncRNAs. Here, we summarized the current understanding of H19 in embryogenesis and development, cancer development and progression, mesenchymal stem cell lineage-specific differentiation, and metabolic diseases. We discussed the potential regulatory mechanisms underlying H19's functions in those processes although more in-depth studies are warranted to delineate the exact molecular, cellular, epigenetic, and genomic regulatory mechanisms underlying the physiological and pathological roles of H19. Ultimately, these lines of investigation may lead to the development of novel therapeutics for human diseases by exploiting H19 functions.
Recent advances in deep sequencing technologies have revealed that, while less than 2% of the human genome is transcribed into mRNA for protein synthesis, over 80% of the genome is transcribed, leading to the production of large amounts of noncoding RNAs (ncRNAs). It has been shown that ncRNAs, especially long non-coding RNAs (lncRNAs), may play crucial regulatory roles in gene expression. As one of the first isolated and reported lncRNAs, H19 has gained much attention due to its essential roles in regulating many physiological and/or pathological processes including embryogenesis, development, tumorigenesis, osteogenesis, and metabolism. Mechanistically, H19 mediates diverse regulatory functions by serving as competing endogenous RNAs (CeRNAs), Igf2/H19 imprinted tandem gene, modular scaffold, cooperating with H19 antisense, and acting directly with other mRNAs or lncRNAs. Here, we summarized the current understanding of H19 in embryogenesis and development, cancer development and progression, mesenchymal stem cell lineage-specific differentiation, and metabolic diseases. We discussed the potential regulatory mechanisms underlying H19's functions in those processes although more in-depth studies are warranted to delineate the exact molecular, cellular, epigenetic, and genomic regulatory mechanisms underlying the physiological and pathological roles of H19. Ultimately, these lines of investigation may lead to the development of novel therapeutics for human diseases by exploiting H19 functions.Recent advances in deep sequencing technologies have revealed that, while less than 2% of the human genome is transcribed into mRNA for protein synthesis, over 80% of the genome is transcribed, leading to the production of large amounts of noncoding RNAs (ncRNAs). It has been shown that ncRNAs, especially long non-coding RNAs (lncRNAs), may play crucial regulatory roles in gene expression. As one of the first isolated and reported lncRNAs, H19 has gained much attention due to its essential roles in regulating many physiological and/or pathological processes including embryogenesis, development, tumorigenesis, osteogenesis, and metabolism. Mechanistically, H19 mediates diverse regulatory functions by serving as competing endogenous RNAs (CeRNAs), Igf2/H19 imprinted tandem gene, modular scaffold, cooperating with H19 antisense, and acting directly with other mRNAs or lncRNAs. Here, we summarized the current understanding of H19 in embryogenesis and development, cancer development and progression, mesenchymal stem cell lineage-specific differentiation, and metabolic diseases. We discussed the potential regulatory mechanisms underlying H19's functions in those processes although more in-depth studies are warranted to delineate the exact molecular, cellular, epigenetic, and genomic regulatory mechanisms underlying the physiological and pathological roles of H19. Ultimately, these lines of investigation may lead to the development of novel therapeutics for human diseases by exploiting H19 functions.
Recent advances in deep sequencing technologies have revealed that, while less than 2% of the human genome is transcribed into mRNA for protein synthesis, over 80% of the genome is transcribed, leading to the production of large amounts of noncoding RNAs (ncRNAs). It has been shown that ncRNAs, especially long non-coding RNAs (lncRNAs), may play crucial regulatory roles in gene expression. As one of the first isolated and reported lncRNAs, 9 has gained much attention due to its essential roles in regulating many physiological and/or pathological processes including embryogenesis, development, tumorigenesis, osteogenesis, and metabolism. Mechanistically, mediates diverse regulatory functions by serving as competing endogenous RNAs (CeRNAs), imprinted tandem gene, modular scaffold, cooperating with antisense, and acting directly with other mRNAs or lncRNAs. Here, we summarized the current understanding of in embryogenesis and development, cancer development and progression, mesenchymal stem cell lineage-specific differentiation, and metabolic diseases. We discussed the potential regulatory mechanisms underlying 's functions in those processes although more in-depth studies are warranted to delineate the exact molecular, cellular, epigenetic, and genomic regulatory mechanisms underlying the physiological and pathological roles of . Ultimately, these lines of investigation may lead to the development of novel therapeutics for human diseases by exploiting functions.
Author Gao, Shengqiang
Chen, Bowen
Zhu, Zhenglin
Wang, Annie
Shi, Lewis
Fan, Jiaming
Song, Lily
Zhao, Guozhi
Reid, Russell R.
He, Tong-Chuan
Zhao, Piao
Wang, Yonghui
Huang, Wei
Schwartz, Zander
Hong, Jeffrey
Haydon, Rex C.
Luu, Hue H.
Du, Chengcheng
Wagstaff, William
Liao, Junyi
Hu, Ning
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  organization: Departments of Orthopedic Surgery and Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China
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  givenname: Piao
  surname: Zhao
  fullname: Zhao, Piao
  organization: Departments of Orthopedic Surgery and Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China
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  givenname: Yonghui
  surname: Wang
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  organization: Molecular Oncology Laboratory, Department of Orthopaedic Surgery and Rehabilitation Medicine, The University of Chicago Medical Center, Chicago, IL 60637, USA
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  givenname: Lily
  surname: Song
  fullname: Song, Lily
  organization: Molecular Oncology Laboratory, Department of Orthopaedic Surgery and Rehabilitation Medicine, The University of Chicago Medical Center, Chicago, IL 60637, USA
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  givenname: Jeffrey
  surname: Hong
  fullname: Hong, Jeffrey
  organization: Molecular Oncology Laboratory, Department of Orthopaedic Surgery and Rehabilitation Medicine, The University of Chicago Medical Center, Chicago, IL 60637, USA
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  surname: Wagstaff
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  surname: Haydon
  fullname: Haydon, Rex C.
  organization: Molecular Oncology Laboratory, Department of Orthopaedic Surgery and Rehabilitation Medicine, The University of Chicago Medical Center, Chicago, IL 60637, USA
– sequence: 15
  givenname: Hue H.
  surname: Luu
  fullname: Luu, Hue H.
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  givenname: Jiaming
  surname: Fan
  fullname: Fan, Jiaming
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  givenname: Tong-Chuan
  surname: He
  fullname: He, Tong-Chuan
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  email: 1276321387@qq.com
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  givenname: Wei
  surname: Huang
  fullname: Huang, Wei
  email: huagnwei68@263.net
  organization: Departments of Orthopedic Surgery and Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China
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Copyright 2023 Chongqing Medical University
2023 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd.
2023 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. 2023 Chongqing Medical University
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Issue 4
Keywords H19
LncRNA
Metabolic diseases
Stem cell differentiation
Epigenetic regulation
Long-noncoding RNA
Cancer
Language English
License This is an open access article under the CC BY-NC-ND license.
2023 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd.
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Snippet Recent advances in deep sequencing technologies have revealed that, while less than 2% of the human genome is transcribed into mRNA for protein synthesis, over...
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SubjectTerms Cancer
Epigenetic regulation
H19
LncRNA
Long-noncoding RNA
Metabolic diseases
Review
Stem cell differentiation
Title Long noncoding RNA (lncRNA) H19: An essential developmental regulator with expanding roles in cancer, stem cell differentiation, and metabolic diseases
URI https://dx.doi.org/10.1016/j.gendis.2023.02.008
https://www.ncbi.nlm.nih.gov/pubmed/37397543
https://www.proquest.com/docview/2832843213
https://pubmed.ncbi.nlm.nih.gov/PMC10311118
https://doaj.org/article/578f419536f7488ab664e00e601ede51
Volume 10
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