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LTA4H extensively associates with mRNAs and lncRNAs indicative of its novel regulatory targets

The RNA-binding metabolic enzyme LTA4H is a novel target for cancer chemoprevention and chemotherapy. Recent research shows that the increased expression of LTA4H in laryngeal squamous cell carcinoma (LSCC) promotes tumor proliferation, migration, and metastasis. However, its mechanism remains uncle...

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Autores principales: Ren, Tianjiao, Wang, Song, Zhang, Bo, Zhou, Wei, Wang, Cansi, Zhao, Xiaorui, Feng, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010175/
https://www.ncbi.nlm.nih.gov/pubmed/36923505
http://dx.doi.org/10.7717/peerj.14875
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author Ren, Tianjiao
Wang, Song
Zhang, Bo
Zhou, Wei
Wang, Cansi
Zhao, Xiaorui
Feng, Juan
author_facet Ren, Tianjiao
Wang, Song
Zhang, Bo
Zhou, Wei
Wang, Cansi
Zhao, Xiaorui
Feng, Juan
author_sort Ren, Tianjiao
collection PubMed
description The RNA-binding metabolic enzyme LTA4H is a novel target for cancer chemoprevention and chemotherapy. Recent research shows that the increased expression of LTA4H in laryngeal squamous cell carcinoma (LSCC) promotes tumor proliferation, migration, and metastasis. However, its mechanism remains unclear. To investigate the potential role of LTA4H in LSCC, we employed the improved RNA immunoprecipitation and sequencing (iRIP-Seq) experiment to get the expression profile of LTA4H binding RNA in HeLa model cells, a cancer model cell that is frequently used in molecular mechanism research. We found that LTA4H extensively binds with mRNAs/pre-mRNAs and lncRNAs. In the LTA4H binding peak, the frequency of the AAGG motif reported to interact with TRA2β4 was high in both replicates. More notably, LTA4H-binding genes were significantly enriched in the mitotic cell cycle, DNA repair, RNA splicing-related pathways, and RNA metabolism pathways, which means that LTA4H has tumor-related alternative splicing regulatory functions. QRT-PCR validation confirmed that LTA4H specifically binds to mRNAs of carcinogenesis-associated genes, including LTBP3, ROR2, EGFR, HSP90B1, and lncRNAs represented by NEAT1. These results suggest that LTA4H may combine with genes associated with LSCC as an RNA-binding protein to perform a cancer regulatory function. Our study further sheds light on the molecular mechanism of LTA4H as a clinical therapy target for LSCC.
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spelling pubmed-100101752023-03-14 LTA4H extensively associates with mRNAs and lncRNAs indicative of its novel regulatory targets Ren, Tianjiao Wang, Song Zhang, Bo Zhou, Wei Wang, Cansi Zhao, Xiaorui Feng, Juan PeerJ Biochemistry The RNA-binding metabolic enzyme LTA4H is a novel target for cancer chemoprevention and chemotherapy. Recent research shows that the increased expression of LTA4H in laryngeal squamous cell carcinoma (LSCC) promotes tumor proliferation, migration, and metastasis. However, its mechanism remains unclear. To investigate the potential role of LTA4H in LSCC, we employed the improved RNA immunoprecipitation and sequencing (iRIP-Seq) experiment to get the expression profile of LTA4H binding RNA in HeLa model cells, a cancer model cell that is frequently used in molecular mechanism research. We found that LTA4H extensively binds with mRNAs/pre-mRNAs and lncRNAs. In the LTA4H binding peak, the frequency of the AAGG motif reported to interact with TRA2β4 was high in both replicates. More notably, LTA4H-binding genes were significantly enriched in the mitotic cell cycle, DNA repair, RNA splicing-related pathways, and RNA metabolism pathways, which means that LTA4H has tumor-related alternative splicing regulatory functions. QRT-PCR validation confirmed that LTA4H specifically binds to mRNAs of carcinogenesis-associated genes, including LTBP3, ROR2, EGFR, HSP90B1, and lncRNAs represented by NEAT1. These results suggest that LTA4H may combine with genes associated with LSCC as an RNA-binding protein to perform a cancer regulatory function. Our study further sheds light on the molecular mechanism of LTA4H as a clinical therapy target for LSCC. PeerJ Inc. 2023-03-10 /pmc/articles/PMC10010175/ /pubmed/36923505 http://dx.doi.org/10.7717/peerj.14875 Text en ©2023 Ren et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Biochemistry
Ren, Tianjiao
Wang, Song
Zhang, Bo
Zhou, Wei
Wang, Cansi
Zhao, Xiaorui
Feng, Juan
LTA4H extensively associates with mRNAs and lncRNAs indicative of its novel regulatory targets
title LTA4H extensively associates with mRNAs and lncRNAs indicative of its novel regulatory targets
title_full LTA4H extensively associates with mRNAs and lncRNAs indicative of its novel regulatory targets
title_fullStr LTA4H extensively associates with mRNAs and lncRNAs indicative of its novel regulatory targets
title_full_unstemmed LTA4H extensively associates with mRNAs and lncRNAs indicative of its novel regulatory targets
title_short LTA4H extensively associates with mRNAs and lncRNAs indicative of its novel regulatory targets
title_sort lta4h extensively associates with mrnas and lncrnas indicative of its novel regulatory targets
topic Biochemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010175/
https://www.ncbi.nlm.nih.gov/pubmed/36923505
http://dx.doi.org/10.7717/peerj.14875
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