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circCIMT Silencing Promotes Cadmium‐Induced Malignant Transformation of Lung Epithelial Cells Through the DNA Base Excision Repair Pathway

Changes in gene expression in lung epithelial cells are detected in cancer tissues during exposure to pollutants, highlighting the importance of gene‐environmental interactions in disease. Here, a Cd‐induced malignant transformation model in mouse lungs and bronchial epithelial cell lines is constru...

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Autores principales: Li, Meizhen, Chen, Wei, Cui, Jinjin, Lin, Qiuyi, Liu, Yufei, Zeng, Huixian, Hua, Qiuhan, Ling, Yihui, Qin, Xiaodi, Zhang, Yindai, Li, Xueqi, Lin, Tianshu, Huang, Lihua, Jiang, Yiguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10190647/
https://www.ncbi.nlm.nih.gov/pubmed/36814305
http://dx.doi.org/10.1002/advs.202206896
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author Li, Meizhen
Chen, Wei
Cui, Jinjin
Lin, Qiuyi
Liu, Yufei
Zeng, Huixian
Hua, Qiuhan
Ling, Yihui
Qin, Xiaodi
Zhang, Yindai
Li, Xueqi
Lin, Tianshu
Huang, Lihua
Jiang, Yiguo
author_facet Li, Meizhen
Chen, Wei
Cui, Jinjin
Lin, Qiuyi
Liu, Yufei
Zeng, Huixian
Hua, Qiuhan
Ling, Yihui
Qin, Xiaodi
Zhang, Yindai
Li, Xueqi
Lin, Tianshu
Huang, Lihua
Jiang, Yiguo
author_sort Li, Meizhen
collection PubMed
description Changes in gene expression in lung epithelial cells are detected in cancer tissues during exposure to pollutants, highlighting the importance of gene‐environmental interactions in disease. Here, a Cd‐induced malignant transformation model in mouse lungs and bronchial epithelial cell lines is constructed, and differences in the expression of non‐coding circRNAs are analyzed. The migratory and invasive abilities of Cd‐transformed cells are suppressed by circCIMT. A significant DNA damage response is observed after exposure to Cd, which increased further following circCIMT‐interference. It is found that APEX1 is significantly down‐regulated following Cd exposure. Furthermore, it is demonstrated that circCIMT bound to APEX1 during Cd exposure to mediate the DNA base excision repair (BER) pathway, thereby reducing DNA damage. In addition, simultaneous knockdown of both circCIMT and APEX1 promotes the expression of cancer‐related genes and malignant transformation after long‐term Cd exposure. Overall, these findings emphasis the importance of genetic‐epigenetic interactions in chemical‐induced cancer transformation.
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spelling pubmed-101906472023-05-18 circCIMT Silencing Promotes Cadmium‐Induced Malignant Transformation of Lung Epithelial Cells Through the DNA Base Excision Repair Pathway Li, Meizhen Chen, Wei Cui, Jinjin Lin, Qiuyi Liu, Yufei Zeng, Huixian Hua, Qiuhan Ling, Yihui Qin, Xiaodi Zhang, Yindai Li, Xueqi Lin, Tianshu Huang, Lihua Jiang, Yiguo Adv Sci (Weinh) Research Articles Changes in gene expression in lung epithelial cells are detected in cancer tissues during exposure to pollutants, highlighting the importance of gene‐environmental interactions in disease. Here, a Cd‐induced malignant transformation model in mouse lungs and bronchial epithelial cell lines is constructed, and differences in the expression of non‐coding circRNAs are analyzed. The migratory and invasive abilities of Cd‐transformed cells are suppressed by circCIMT. A significant DNA damage response is observed after exposure to Cd, which increased further following circCIMT‐interference. It is found that APEX1 is significantly down‐regulated following Cd exposure. Furthermore, it is demonstrated that circCIMT bound to APEX1 during Cd exposure to mediate the DNA base excision repair (BER) pathway, thereby reducing DNA damage. In addition, simultaneous knockdown of both circCIMT and APEX1 promotes the expression of cancer‐related genes and malignant transformation after long‐term Cd exposure. Overall, these findings emphasis the importance of genetic‐epigenetic interactions in chemical‐induced cancer transformation. John Wiley and Sons Inc. 2023-02-22 /pmc/articles/PMC10190647/ /pubmed/36814305 http://dx.doi.org/10.1002/advs.202206896 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Li, Meizhen
Chen, Wei
Cui, Jinjin
Lin, Qiuyi
Liu, Yufei
Zeng, Huixian
Hua, Qiuhan
Ling, Yihui
Qin, Xiaodi
Zhang, Yindai
Li, Xueqi
Lin, Tianshu
Huang, Lihua
Jiang, Yiguo
circCIMT Silencing Promotes Cadmium‐Induced Malignant Transformation of Lung Epithelial Cells Through the DNA Base Excision Repair Pathway
title circCIMT Silencing Promotes Cadmium‐Induced Malignant Transformation of Lung Epithelial Cells Through the DNA Base Excision Repair Pathway
title_full circCIMT Silencing Promotes Cadmium‐Induced Malignant Transformation of Lung Epithelial Cells Through the DNA Base Excision Repair Pathway
title_fullStr circCIMT Silencing Promotes Cadmium‐Induced Malignant Transformation of Lung Epithelial Cells Through the DNA Base Excision Repair Pathway
title_full_unstemmed circCIMT Silencing Promotes Cadmium‐Induced Malignant Transformation of Lung Epithelial Cells Through the DNA Base Excision Repair Pathway
title_short circCIMT Silencing Promotes Cadmium‐Induced Malignant Transformation of Lung Epithelial Cells Through the DNA Base Excision Repair Pathway
title_sort circcimt silencing promotes cadmium‐induced malignant transformation of lung epithelial cells through the dna base excision repair pathway
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10190647/
https://www.ncbi.nlm.nih.gov/pubmed/36814305
http://dx.doi.org/10.1002/advs.202206896
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