SOX9 promotes tumor progression through the axis BMI1-p21CIP

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Main Authors: Aldaz, Paula, Otaegi, Maddalen, Saenz-Antoñanzas, Ander, García-Puga, Mikel, Moreno Valladares, Manuel, Flores, Juana M, Gerovska, Daniela, Araúzo-Bravo, Marcos J., Sampron, Nicolas, Matheu, Ander, Carrasco García, Estefanía
Format: Recurso digital
Language:English
Published: Zenodo 2020
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author Aldaz, Paula
Otaegi, Maddalen
Saenz-Antoñanzas, Ander
García-Puga, Mikel
Moreno Valladares, Manuel
Flores, Juana M
Gerovska, Daniela
Araúzo-Bravo, Marcos J.
Sampron, Nicolas
Matheu, Ander
Carrasco García, Estefanía
author_facet Aldaz, Paula
Otaegi, Maddalen
Saenz-Antoñanzas, Ander
García-Puga, Mikel
Moreno Valladares, Manuel
Flores, Juana M
Gerovska, Daniela
Araúzo-Bravo, Marcos J.
Sampron, Nicolas
Matheu, Ander
Carrasco García, Estefanía
contents <div> <div> <p>The developmental regulator SOX9 is linked to cancer progression mainly as a result of its role in the regulation of cancer stem cells (CSCs). However, its activity in the differentiated cells that constitute the heterogeneous tumor bulk has not been extensively studied. In this work, we addressed this aspect in gastric cancer, glioblastoma and pancreatic adenocarcinoma. SOX9 silencing studies revealed that SOX9 is required for cancer cell survival, proliferation and evasion of senescence in vitro and tumor growth in vivo. Gain of-SOX9 function showed that high levels of SOX9 promote tumor cell proliferation in vitro and in vivo. Mechanistically, the modulation of SOX9 changed the expression of the transcriptional repressor BMI1 in the same direction in the three types of cancer, and the expression of the tumor suppressor p21<sup>CIP</sup> in the opposite direction. In agreement with this, SOX9 expression positively correlated with BMI1 levels and inversely with p21<sup>CIP</sup> in clinical samples of the different cancers. Moreover, BMI1 re-establishment in SOX9-silenced tumor cells restored cell viability and proliferation as well as decreased p21<sup>CIP</sup> in vitro and tumor growth in vivo. These results indicate that BMI1 is a critical effector of the pro-tumoral activity of SOX9 in tumor bulk cells through the repression of p21<sup>CIP</sup>. Our results highlight the relevance of the SOX9-BMI1-p21<sup>CIP</sup> axis in tumor progression, shedding novel opportunities for therapeutic development.</p> </div> </div>
format Recurso digital
id zenodo_https___doi_org_10_1038_s41598-019-57047-w
institution Zenodo
language eng
publishDate 2020
publisher Zenodo
record_format zenodo
spellingShingle SOX9 promotes tumor progression through the axis BMI1-p21CIP
Aldaz, Paula
Otaegi, Maddalen
Saenz-Antoñanzas, Ander
García-Puga, Mikel
Moreno Valladares, Manuel
Flores, Juana M
Gerovska, Daniela
Araúzo-Bravo, Marcos J.
Sampron, Nicolas
Matheu, Ander
Carrasco García, Estefanía
SOX9
cancer
biomarkers
<div> <div> <p>The developmental regulator SOX9 is linked to cancer progression mainly as a result of its role in the regulation of cancer stem cells (CSCs). However, its activity in the differentiated cells that constitute the heterogeneous tumor bulk has not been extensively studied. In this work, we addressed this aspect in gastric cancer, glioblastoma and pancreatic adenocarcinoma. SOX9 silencing studies revealed that SOX9 is required for cancer cell survival, proliferation and evasion of senescence in vitro and tumor growth in vivo. Gain of-SOX9 function showed that high levels of SOX9 promote tumor cell proliferation in vitro and in vivo. Mechanistically, the modulation of SOX9 changed the expression of the transcriptional repressor BMI1 in the same direction in the three types of cancer, and the expression of the tumor suppressor p21<sup>CIP</sup> in the opposite direction. In agreement with this, SOX9 expression positively correlated with BMI1 levels and inversely with p21<sup>CIP</sup> in clinical samples of the different cancers. Moreover, BMI1 re-establishment in SOX9-silenced tumor cells restored cell viability and proliferation as well as decreased p21<sup>CIP</sup> in vitro and tumor growth in vivo. These results indicate that BMI1 is a critical effector of the pro-tumoral activity of SOX9 in tumor bulk cells through the repression of p21<sup>CIP</sup>. Our results highlight the relevance of the SOX9-BMI1-p21<sup>CIP</sup> axis in tumor progression, shedding novel opportunities for therapeutic development.</p> </div> </div>
title SOX9 promotes tumor progression through the axis BMI1-p21CIP
topic SOX9
cancer
biomarkers
url https://doi.org/10.1038/s41598-019-57047-w