Regulatory Role of the RUNX2 Transcription Factor in Lung Cancer Apoptosis

Lung cancer is the leading cause of cancer death globally. Numerous factors intervene in the onset and progression of lung tumors, among which the participation of lineage-specific transcription factors stands out. Several transcription factors important in embryonic development are abnormally expre...

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Main Authors: Camila Bernal, Andrea Otalora, Alejandra Cañas, Alfonso Barreto, Karol Prieto, Martin Montecino, Adriana Rojas
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:International Journal of Cell Biology
Online Access:http://dx.doi.org/10.1155/2022/5198203
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author Camila Bernal
Andrea Otalora
Alejandra Cañas
Alfonso Barreto
Karol Prieto
Martin Montecino
Adriana Rojas
author_facet Camila Bernal
Andrea Otalora
Alejandra Cañas
Alfonso Barreto
Karol Prieto
Martin Montecino
Adriana Rojas
author_sort Camila Bernal
collection DOAJ
description Lung cancer is the leading cause of cancer death globally. Numerous factors intervene in the onset and progression of lung tumors, among which the participation of lineage-specific transcription factors stands out. Several transcription factors important in embryonic development are abnormally expressed in adult tissues and thus participate in the activation of signaling pathways related to the acquisition of the tumor phenotype. RUNX2 is the transcription factor responsible for osteogenic differentiation in mammals. Current studies have confirmed that RUNX2 is closely related to the proliferation, invasion, and bone metastasis of multiple cancer types, such as osteosarcoma, breast cancer (BC), prostate cancer, gastric cancer, colorectal cancer, and lung cancer. Thus, the present study is aimed at evaluating the role of the RUNX2 transcription factor in inhibiting the apoptosis process. Loss-of-function assays using sh-RNA from lentiviral particles and coupled with Annexin/propidium iodide (PI) assays (flow cytometry), immunofluorescence, and quantitative PCR analysis of genes related to cell apoptosis (BAD, BAX, BCL2, BCL-XL, and MCL1) were performed. Silencing assays and Annexin/PI assays demonstrated that when RUNX2 was absent, the percentage of dead cells increased, and the expression levels of the BCL2, BCL-XL, and MCL1 genes were downregulated. Furthermore, to confirm whether the regulatory role of RUNX2 in the expression of these genes is related to its binding to the promoter region, we performed chromatin immunoprecipitation (ChIP) assays. Here, we report that overexpression of the RUNX2 gene in lung cancer may be related to the inhibition of the intrinsic apoptosis pathway, specifically, through direct transcriptional regulation of the antiapoptotic gene BCL2 and indirect regulation of BCL-XL and MCL1.
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spelling doaj-art-84337eacbc56420e910999d93969da272025-02-03T05:57:56ZengWileyInternational Journal of Cell Biology1687-88842022-01-01202210.1155/2022/5198203Regulatory Role of the RUNX2 Transcription Factor in Lung Cancer ApoptosisCamila Bernal0Andrea Otalora1Alejandra Cañas2Alfonso Barreto3Karol Prieto4Martin Montecino5Adriana Rojas6Institute of Human GeneticsInstitute of Human GeneticsInternal Medicine DepartmentImmunology and Cellular Biology Research GroupImmunology and Cellular Biology Research GroupInstitute of Biomedical SciencesInstitute of Human GeneticsLung cancer is the leading cause of cancer death globally. Numerous factors intervene in the onset and progression of lung tumors, among which the participation of lineage-specific transcription factors stands out. Several transcription factors important in embryonic development are abnormally expressed in adult tissues and thus participate in the activation of signaling pathways related to the acquisition of the tumor phenotype. RUNX2 is the transcription factor responsible for osteogenic differentiation in mammals. Current studies have confirmed that RUNX2 is closely related to the proliferation, invasion, and bone metastasis of multiple cancer types, such as osteosarcoma, breast cancer (BC), prostate cancer, gastric cancer, colorectal cancer, and lung cancer. Thus, the present study is aimed at evaluating the role of the RUNX2 transcription factor in inhibiting the apoptosis process. Loss-of-function assays using sh-RNA from lentiviral particles and coupled with Annexin/propidium iodide (PI) assays (flow cytometry), immunofluorescence, and quantitative PCR analysis of genes related to cell apoptosis (BAD, BAX, BCL2, BCL-XL, and MCL1) were performed. Silencing assays and Annexin/PI assays demonstrated that when RUNX2 was absent, the percentage of dead cells increased, and the expression levels of the BCL2, BCL-XL, and MCL1 genes were downregulated. Furthermore, to confirm whether the regulatory role of RUNX2 in the expression of these genes is related to its binding to the promoter region, we performed chromatin immunoprecipitation (ChIP) assays. Here, we report that overexpression of the RUNX2 gene in lung cancer may be related to the inhibition of the intrinsic apoptosis pathway, specifically, through direct transcriptional regulation of the antiapoptotic gene BCL2 and indirect regulation of BCL-XL and MCL1.http://dx.doi.org/10.1155/2022/5198203
spellingShingle Camila Bernal
Andrea Otalora
Alejandra Cañas
Alfonso Barreto
Karol Prieto
Martin Montecino
Adriana Rojas
Regulatory Role of the RUNX2 Transcription Factor in Lung Cancer Apoptosis
International Journal of Cell Biology
title Regulatory Role of the RUNX2 Transcription Factor in Lung Cancer Apoptosis
title_full Regulatory Role of the RUNX2 Transcription Factor in Lung Cancer Apoptosis
title_fullStr Regulatory Role of the RUNX2 Transcription Factor in Lung Cancer Apoptosis
title_full_unstemmed Regulatory Role of the RUNX2 Transcription Factor in Lung Cancer Apoptosis
title_short Regulatory Role of the RUNX2 Transcription Factor in Lung Cancer Apoptosis
title_sort regulatory role of the runx2 transcription factor in lung cancer apoptosis
url http://dx.doi.org/10.1155/2022/5198203
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AT alfonsobarreto regulatoryroleoftherunx2transcriptionfactorinlungcancerapoptosis
AT karolprieto regulatoryroleoftherunx2transcriptionfactorinlungcancerapoptosis
AT martinmontecino regulatoryroleoftherunx2transcriptionfactorinlungcancerapoptosis
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