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Differential effects of WRAP53 transcript variants on non-small cell lung cancer cell behaviors

BACKGROUND: The WD40-encoding RNA antisense to p53 (WRAP53) is an antisense gene of TP53 with three transcriptional start sites producing three transcript variants involved in the progression of non-small cell lung cancer. However, the mechanism by which these different transcript variants regulate...

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Autores principales: Zhu, Yan, Sun, Wenjie, Jiang, Xueping, Bai, Rui, Luo, Yuan, Gao, Yanping, Li, Shuying, Huang, Zhengrong, Gong, Yan, Xie, Conghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9882892/
https://www.ncbi.nlm.nih.gov/pubmed/36706151
http://dx.doi.org/10.1371/journal.pone.0281132
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author Zhu, Yan
Sun, Wenjie
Jiang, Xueping
Bai, Rui
Luo, Yuan
Gao, Yanping
Li, Shuying
Huang, Zhengrong
Gong, Yan
Xie, Conghua
author_facet Zhu, Yan
Sun, Wenjie
Jiang, Xueping
Bai, Rui
Luo, Yuan
Gao, Yanping
Li, Shuying
Huang, Zhengrong
Gong, Yan
Xie, Conghua
author_sort Zhu, Yan
collection PubMed
description BACKGROUND: The WD40-encoding RNA antisense to p53 (WRAP53) is an antisense gene of TP53 with three transcriptional start sites producing three transcript variants involved in the progression of non-small cell lung cancer. However, the mechanism by which these different transcript variants regulate non-small cell lung cancer cell behaviors is to be elucidated. METHODS: Two non-small cell lung cancer cell lines, A549 cells with wild-type p53 and H1975 with mutated p53, were transfected with WRAP53-1α and WRAP53-1β siRNA. The biological effects were assessed via colony formation, cell viability, apoptosis, cell cycle, wound healing and cell invasion assays, as well as immunoblotting. RESULTS: Knockdown of WRAP53-1α increased the mRNA and protein levels of p53; suppressed colony formation and proliferation of A549 cells but promoted them in H1975 cells; increased the proportion of cells in the G0/G1 phase in A549 cells but decreased that in H1975 cells; and suppressed migration and invasion in A549 cells but not in H1975 cells. Conversely, knockdown of WRAP53-1β had no effect on p53 expression; promoted the growth of A549 cells but not of H1975 cells; decreased the proportion of cells in the G0/G1 phase in A549 cells but not in H1975 cells; and promoted migration and invasion in A549 cells but not in H1975 cells. Knockdown of both WRAP53-1α and WRAP53-1β promoted apoptosis in A549 cells but not in H1975 cells. CONCLUSIONS: WRAP53 transcript variants exerted different functions in non-small cell lung cancer cells and regulated non-small cell lung cancer cell behaviors depending on the p53 expression.
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spelling pubmed-98828922023-01-28 Differential effects of WRAP53 transcript variants on non-small cell lung cancer cell behaviors Zhu, Yan Sun, Wenjie Jiang, Xueping Bai, Rui Luo, Yuan Gao, Yanping Li, Shuying Huang, Zhengrong Gong, Yan Xie, Conghua PLoS One Research Article BACKGROUND: The WD40-encoding RNA antisense to p53 (WRAP53) is an antisense gene of TP53 with three transcriptional start sites producing three transcript variants involved in the progression of non-small cell lung cancer. However, the mechanism by which these different transcript variants regulate non-small cell lung cancer cell behaviors is to be elucidated. METHODS: Two non-small cell lung cancer cell lines, A549 cells with wild-type p53 and H1975 with mutated p53, were transfected with WRAP53-1α and WRAP53-1β siRNA. The biological effects were assessed via colony formation, cell viability, apoptosis, cell cycle, wound healing and cell invasion assays, as well as immunoblotting. RESULTS: Knockdown of WRAP53-1α increased the mRNA and protein levels of p53; suppressed colony formation and proliferation of A549 cells but promoted them in H1975 cells; increased the proportion of cells in the G0/G1 phase in A549 cells but decreased that in H1975 cells; and suppressed migration and invasion in A549 cells but not in H1975 cells. Conversely, knockdown of WRAP53-1β had no effect on p53 expression; promoted the growth of A549 cells but not of H1975 cells; decreased the proportion of cells in the G0/G1 phase in A549 cells but not in H1975 cells; and promoted migration and invasion in A549 cells but not in H1975 cells. Knockdown of both WRAP53-1α and WRAP53-1β promoted apoptosis in A549 cells but not in H1975 cells. CONCLUSIONS: WRAP53 transcript variants exerted different functions in non-small cell lung cancer cells and regulated non-small cell lung cancer cell behaviors depending on the p53 expression. Public Library of Science 2023-01-27 /pmc/articles/PMC9882892/ /pubmed/36706151 http://dx.doi.org/10.1371/journal.pone.0281132 Text en © 2023 Zhu 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, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Zhu, Yan
Sun, Wenjie
Jiang, Xueping
Bai, Rui
Luo, Yuan
Gao, Yanping
Li, Shuying
Huang, Zhengrong
Gong, Yan
Xie, Conghua
Differential effects of WRAP53 transcript variants on non-small cell lung cancer cell behaviors
title Differential effects of WRAP53 transcript variants on non-small cell lung cancer cell behaviors
title_full Differential effects of WRAP53 transcript variants on non-small cell lung cancer cell behaviors
title_fullStr Differential effects of WRAP53 transcript variants on non-small cell lung cancer cell behaviors
title_full_unstemmed Differential effects of WRAP53 transcript variants on non-small cell lung cancer cell behaviors
title_short Differential effects of WRAP53 transcript variants on non-small cell lung cancer cell behaviors
title_sort differential effects of wrap53 transcript variants on non-small cell lung cancer cell behaviors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9882892/
https://www.ncbi.nlm.nih.gov/pubmed/36706151
http://dx.doi.org/10.1371/journal.pone.0281132
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