Morgan, Richard ORCID: https://orcid.org/0000-0002-8721-4479, Simpson, Guy, Gray, Sophie, Gillett, Cheryl, Tabi, Zsuzsanna, Spicer, James, Harrington, Kevin and Pandha, Hardev (2016) HOX transcription factors are potential targets and markers in malignant mesothelioma. BMC cancer, 16 (1).

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Abstract

Background The HOX genes are a family of homeodomain-containing transcription factors that determine cellular identity during development and which are dys-regulated in some cancers. In this study we examined the expression and oncogenic function of HOX genes in mesothelioma, a cancer arising from the pleura or peritoneum which is associated with exposure to asbestos.
Methods We tested the sensitivity of the mesothelioma-derived lines MSTO-211H, NCI-H28, NCI-H2052, and NCI-H226 to HXR9, a peptide antagonist of HOX protein binding to its PBX co-factor. Apoptosis was measured using a FACS-based assay with Annexin, and HOX gene expression profiles were established using RT-QPCR on RNA extracted from cell lines and primary mesotheliomas. The in vivo efficacy of HXR9 was tested in a mouse MSTO-211H flank tumor xenograft model.
Results We show that HOX genes are significantly dysregulated in malignant mesothelioma. Targeting HOX genes with HXR9 caused apoptotic cell death in all of the mesothelioma-derived cell lines, and prevented the growth of mesothelioma tumors in a mouse xenograft model. Furthermore, the sensitivity of these lines to HXR9 correlated with the relative expression of HOX genes that have either an oncogenic or tumor suppressive function in cancer. The analysis of HOX expression in primary mesothelioma tumors indicated that these cells could also be sensitive to the disruption of HOX activity by HXR9, and that the expression of HOXB4 is strongly associated with overall survival.
Conclusion HOX genes are a potential therapeutic target in mesothelioma, and HOXB4 expression correlates with overall survival.

Item Type:	Article
Identifier:	10.1186/s12885-016-2106-7
Keywords:	Mesothelioma, HOX genes, HXR9, HOXB4, Overall survival
Subjects:	Natural sciences > Cell and molecular biology
Related URLs:	Organisation Publisher
Depositing User:	Richard Morgan
Date Deposited:	08 Jul 2020 14:26
Last Modified:	06 Feb 2024 16:03
URI:	https://repository.uwl.ac.uk/id/eprint/7107

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