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PTEN, ERG, SPINK1, and TFF3 Status and Relationship in a Prostate Cancer Cohort from Jordanian Arab Population.

Samir Al BashirMohammed S AlorjaniKhalid Ahmed KheirallahMohammad Abdelqader Al HamadHusam K HaddadAhmad Al-DwairyBaha A Bani-FawwazNajla AldaoudOmar HalalshehSaddam AmawiIsmail I Matalka
Published in: Medicina (Kaunas, Lithuania) (2024)
Background and Objectives : Prognostic biomarkers in prostate cancer (PCa) include PTEN, ERG, SPINK1, and TFF3. Their relationships and patterns of expression in PCa in developing countries, including Jordan, have not yet been investigated. Materials and Methods : A tissue microarray (TMA) of PCa patients was taken from paraffin-embedded tissue blocks for 130 patients. PTEN, ERG, SPINK1, and TFF3 expression profiles were examined using immunohistochemistry (IHC) and correlated with each other and other clinicopathological factors. Results : PTEN loss of any degree was observed in 42.9% of PCa cases. ERG and TFF3 were expressed in 59.3% and 46.5% of PCa cases, respectively. SPINK1 expression was observed in 6 out of 104 PCa cases (5.4%). Among all PCa cases ( n = 104), 3.8% ( n = 4) showed SPINK1+/ERG+ phenotype, 1.9% ( n = 2) showed SPINK1+/ERG- phenotype, 56.7% ( n = 59) showed SPINK1-/ERG+ phenotype, and 37.5% showed SPINK1-/ERG- phenotype ( n = 39). Among ERG positive cases ( n = 63), 6.3% were SPINK1 positive. Among SPINK1 positive cases ( n = 6), 66.7% were ERG positive. SPINK1 expression was predominantly observed in a subgroup of cancers that expressed TFF3 (6/6). Additionally, a statistically significant loss of PTEN expression was observed from Gleason Score 6 (GS6) (Grade Group 1 (GG1)) to GS9-10 (GG5); ( p -value 0.019). Conclusions : This is the first study to look at the status of the PTEN, ERG, SPINK1, and TFF3 genes in a Jordanian Arab population. Loss of PTEN has been linked to more aggressive prostate cancer with high GSs/GGs. SPINK1 expression was predominantly observed in a subgroup of cancers that expressed TFF3. Our results call for screening these biomarkers for grading and molecular subtyping of the disease.
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