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PAIP1 regulates expression of immune and inflammatory response associated genes at transcript level in liver cancer cell

Poly(A) binding protein interacting protein 1 (PAIP1) is a translation regulator and also regulate the decay of mRNA. PAIP1 has also been reported to be a marker of increased invasive potential of liver cancer. However, the roles and underlying molecular mechanism of PAIP1 in liver cancer is still u...

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Autores principales: Zheng, Jianfeng, Fan, Weiwei, Zhang, Xiaoyu, Quan, Weili, Wu, Yunfei, Shu, Mengni, Chen, Moyang, Liang, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10124545/
https://www.ncbi.nlm.nih.gov/pubmed/37101794
http://dx.doi.org/10.7717/peerj.15070
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author Zheng, Jianfeng
Fan, Weiwei
Zhang, Xiaoyu
Quan, Weili
Wu, Yunfei
Shu, Mengni
Chen, Moyang
Liang, Ming
author_facet Zheng, Jianfeng
Fan, Weiwei
Zhang, Xiaoyu
Quan, Weili
Wu, Yunfei
Shu, Mengni
Chen, Moyang
Liang, Ming
author_sort Zheng, Jianfeng
collection PubMed
description Poly(A) binding protein interacting protein 1 (PAIP1) is a translation regulator and also regulate the decay of mRNA. PAIP1 has also been reported to be a marker of increased invasive potential of liver cancer. However, the roles and underlying molecular mechanism of PAIP1 in liver cancer is still unclear. Here, cell viability and the gene expression profile of liver cancer line HepG2 transfected with PAIP1 siRNA was compared with cells transfected with non-targeting control siRNA. The results showed that PAIP1 knockdown inhibited cell viability, and extensively affects expression of 893 genes at transcriptional level in HepG2 cells. Gene function analysis showed that a large number of PAIP1 up-regulated genes were enriched in term of DNA-dependent transcription and the down-regulated genes were enriched in some pathways including immune response and inflammatory response. qPCR confirmed that PAIP1 knockdown positively regulated the expression of selected immune and inflammatory factor genes in HepG2 cells. Expression analysis of TCGA revealed that PAIP1 had positive correlations with two immune associated genes IL1R2 and PTAFR in liver tumor tissue. Taken together, our results demonstrated that PAIP1 was not only a translation regulator, but also a transcription regulator in liver cancer. Moreover, PAIP1 could function as a regulatory factor of immune and inflammatory genes in liver cancer. Thus, our study provides important cues for further study on the regulatory mechanism of PAIP1 in liver cancer.
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spelling pubmed-101245452023-04-25 PAIP1 regulates expression of immune and inflammatory response associated genes at transcript level in liver cancer cell Zheng, Jianfeng Fan, Weiwei Zhang, Xiaoyu Quan, Weili Wu, Yunfei Shu, Mengni Chen, Moyang Liang, Ming PeerJ Biochemistry Poly(A) binding protein interacting protein 1 (PAIP1) is a translation regulator and also regulate the decay of mRNA. PAIP1 has also been reported to be a marker of increased invasive potential of liver cancer. However, the roles and underlying molecular mechanism of PAIP1 in liver cancer is still unclear. Here, cell viability and the gene expression profile of liver cancer line HepG2 transfected with PAIP1 siRNA was compared with cells transfected with non-targeting control siRNA. The results showed that PAIP1 knockdown inhibited cell viability, and extensively affects expression of 893 genes at transcriptional level in HepG2 cells. Gene function analysis showed that a large number of PAIP1 up-regulated genes were enriched in term of DNA-dependent transcription and the down-regulated genes were enriched in some pathways including immune response and inflammatory response. qPCR confirmed that PAIP1 knockdown positively regulated the expression of selected immune and inflammatory factor genes in HepG2 cells. Expression analysis of TCGA revealed that PAIP1 had positive correlations with two immune associated genes IL1R2 and PTAFR in liver tumor tissue. Taken together, our results demonstrated that PAIP1 was not only a translation regulator, but also a transcription regulator in liver cancer. Moreover, PAIP1 could function as a regulatory factor of immune and inflammatory genes in liver cancer. Thus, our study provides important cues for further study on the regulatory mechanism of PAIP1 in liver cancer. PeerJ Inc. 2023-04-21 /pmc/articles/PMC10124545/ /pubmed/37101794 http://dx.doi.org/10.7717/peerj.15070 Text en ©2023 Zheng 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
Zheng, Jianfeng
Fan, Weiwei
Zhang, Xiaoyu
Quan, Weili
Wu, Yunfei
Shu, Mengni
Chen, Moyang
Liang, Ming
PAIP1 regulates expression of immune and inflammatory response associated genes at transcript level in liver cancer cell
title PAIP1 regulates expression of immune and inflammatory response associated genes at transcript level in liver cancer cell
title_full PAIP1 regulates expression of immune and inflammatory response associated genes at transcript level in liver cancer cell
title_fullStr PAIP1 regulates expression of immune and inflammatory response associated genes at transcript level in liver cancer cell
title_full_unstemmed PAIP1 regulates expression of immune and inflammatory response associated genes at transcript level in liver cancer cell
title_short PAIP1 regulates expression of immune and inflammatory response associated genes at transcript level in liver cancer cell
title_sort paip1 regulates expression of immune and inflammatory response associated genes at transcript level in liver cancer cell
topic Biochemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10124545/
https://www.ncbi.nlm.nih.gov/pubmed/37101794
http://dx.doi.org/10.7717/peerj.15070
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