Differential Protein Expression Patterns of HOXA13 and HOXB13 Are Associated with Bladder Cancer Progression

Author:

Chin Fee-Wai1ORCID,Hussin Huzlinda2ORCID,Chau De-Ming1,Ong Teng-Aik3,Yunus Rosna4,Abdul Razack Azad Hassan3,Yusoff Khatijah56,Chan Soon-Choy67ORCID,Veerakumarasivam Abhi168

Affiliation:

1. Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia (UPM), Serdang 43400, Selangor, Malaysia

2. Department of Pathology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia (UPM), Serdang 43400, Selangor, Malaysia

3. Department of Surgery, Faculty of Medicine, Universiti Malaya, Kuala Lumpur 50603, Malaysia

4. Department of Pathology, Hospital Kuala Lumpur, Kuala Lumpur 50586, Malaysia

5. Department of Microbiology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia (UPM), Serdang 43400, Selangor, Malaysia

6. Malaysia Genome and Vaccine Institute, National Institutes of Biotechnology Malaysia, Kajang 43000, Selangor, Malaysia

7. School of Liberal Arts, Science and Technology, Perdana University, Kuala Lumpur 50490, Malaysia

8. School of Medical and Life Sciences, Sunway University, Bandar Sunway 47500, Selangor, Malaysia

Abstract

Bladder cancer is a common urological cancer and has the highest recurrence rate of any cancer. The aim of our study was to profile and characterize the protein expression of homeobox A13 (HOXA13) and homeobox B13 (HOXB13) genes in Malaysian bladder cancer patients. The protein expression of HOXA13 and HOXB13 in formalin-fixed paraffin-embedded (FFPE) bladder cancer tissues was determined by immunohistochemistry (IHC) analysis. The association between HOXA13/HOXB13 protein expression and demographic/clinicopathological characteristics of the bladder cancer patients was determined by chi-square analysis. Approximately 63.6% of the bladder cancer tissues harbored high HOXA13 expression. High HOXA13 expression was significantly associated with non-muscle invasive bladder cancer, lower tumor grade, higher number of lymph node metastases, and recurrence risk. In contrast, low HOXB13 expression (including those with negative expression) was observed in 71.6% of the bladder cancer tissues analyzed. Low HOXB13 expression was significantly associated with muscle-invasive bladder cancer, higher tumor stage, tumor grade, and metastatic risk. Both HOXA13 and HOXB13 protein expression were found to be associated with bladder tumorigenesis. The putative oncogenic and tumor suppressive roles of HOXA13 and HOXB13, respectively, suggest their potential utility as biomarkers in bladder cancer.

Funder

Ministry of Higher Education, Malaysia

the Ministry of Energy, Science, Technology, Environmental and Climate Change, Malaysia

MyBrain15 scholarship awarded by the Ministry of Higher Education, Malaysia

Publisher

MDPI AG

Subject

Clinical Biochemistry

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