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Abstract 6432: Co-expression of HERV-R, CCND1, BRAF, FOXA1, TMPRSS2, ATF4 and low expression of BAZ1B and KMT2D is associated with early detection and poor prognosis of prostate cancer in African Black men from Nigeria

Mohammed, Faruk, Stawiski, Konrad, Musa, Halimatu Sadiya, Owolabi, Sani Kamarudeen, Abubakar, Sani, Rotimi, Solomon O., Umar, Adoke Kasimu, Iliyasu, Yawale, Bello, Ahmad, Odedina, Folakemi T., Yates, Clayton C., Petrie, Kevin, Huang, Franklin W. and Ibrahim, Sani (2024) Abstract 6432: Co-expression of HERV-R, CCND1, BRAF, FOXA1, TMPRSS2, ATF4 and low expression of BAZ1B and KMT2D is associated with early detection and poor prognosis of prostate cancer in African Black men from Nigeria. Cancer Research, 84 (6_Supp). p. 6432. ISSN 1538-7445

Item Type: Article

Abstract

Prostate cancer (CaP) is a heterogeneous disease characterized by features of non-aggressive, slow-growing disorders to fast-growing disease. Men of African ancestry have disproportionately higher incidence and mortality rates for CaP than men of European ancestry. While there is evidence for a higher genetic predisposition for incidence of CaP in men of African ancestry compared to men of European ancestry, there is paucity of molecular biology and transcriptomic studies on the role of Human endogenous retroviruses (HERVs) in relation to CaP-associated genes in CaP pathogenesis and prognosis. In this study, we performed bulk RNA sequencing (RNA‐seq) on formalin‐fixed paraffin‐embeded (FFPE) CaP samples from Nigerian CaP patients to investigate the expression significance of HERV-R in relation to FOXA1, TMPRSS2, BAZ1B, KMT2D, ATF4 and BRAF genes. Based on this findings, we used immunohistochemistry (IHC), enzyme-linked immunosorbent assay (ELISA) and immunofluorescence (IF) to confirm the expression pattern of the HERV-R and FOXA1, TMPRSS2, BAZ1B, KMT2D, ATF4 and BRAF proteins on 45 FFPE CaP and blood plasma samples, and 5 CaP-free samples from patients in Zaria, Nigeria. Most of these patients were longitudinally followed from 2017 to date. The DESeq2 procedure was used for data processing, analysis, and differential expression analysis of the aforementioned genes. We found a significant expression of HERV-R in relation with FOXA1, TMPRSS2, BAZ1B, KMT2D, ATF4, CCND1 and BRAF in the CaP from rural Africans in Nigeria. HERV-R expression was found to be associated with increased PSA level, higher Gleason grade and poor prognosis of CaP. A CaP sample from an 80-year-old patient that was histologically diagnosed to have no malignancy seen despite high PSA level of >100 and poor disease outcomes shows a significant cytoplasmic expression of HERV-R, indicating that HERV-R may serve as an important biomarker for early detection. Unfortunately, we lost the 80-year-old patient to late detection before revisiting his case for proper histological diagnosis and management. In addition, some histologically diagnosed BPH samples that are apparently reported to be CaP-free show stromal cells expression of HERV-R and in some cases show expression of HERV-R in the prostatic glandular areas. In contrast, stromal cells of the CaP samples show no expression of HERV-R, but strong expression in the glandular areas. This may implicate a gradual transition from benign prostatic lesion to malignant prostatic disease. HERV-R expression in CaP may have a relationship with BRAF, CCND1, FOXA1, TMPRSS2 and ATF4 genes. These findings combined together, underscore the importance of the expanded concept of HERV-R expression and CaP associated genes in early detection of CaP and prognosis.

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More Information

Depositing User: Kevin Petrie

Identifiers

Item ID: 17903
Identification Number: https://doi.org/10.1158/1538-7445.AM2024-6432
ISSN: 1538-7445
URI: http://sure.sunderland.ac.uk/id/eprint/17903
Official URL: http://dx.doi.org/10.1158/1538-7445.AM2024-6432

Users with ORCIDS

ORCID for Faruk Mohammed: ORCID iD orcid.org/0000-0003-2319-8948
ORCID for Kevin Petrie: ORCID iD orcid.org/0000-0002-9805-9152

Catalogue record

Date Deposited: 23 Jul 2024 15:02
Last Modified: 23 Jul 2024 15:02

Contributors

Author: Faruk Mohammed ORCID iD
Author: Kevin Petrie ORCID iD
Author: Konrad Stawiski
Author: Halimatu Sadiya Musa
Author: Sani Kamarudeen Owolabi
Author: Sani Abubakar
Author: Solomon O. Rotimi
Author: Adoke Kasimu Umar
Author: Yawale Iliyasu
Author: Ahmad Bello
Author: Folakemi T. Odedina
Author: Clayton C. Yates
Author: Franklin W. Huang
Author: Sani Ibrahim

University Divisions

Faculty of Health Sciences and Wellbeing > School of Medicine

Subjects

Sciences > Biomedical Sciences
Sciences > Health Sciences

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