ALPHA-METHYLACL-COA RACEMASE (AMACR) EXPRESSION IN PROSTATE CANCER AND ITS ASSOCIATION WITH GLEASON GRADE & OTHER HISTOMORPHOLOGICAL PARAMETERS: AN IMMUNOHISTOCHEMICALLY ANALYSIS

Main Article Content

Bayyanah Batool
Dr. Sadaf Shaheen
Dr. Abdul Sattar Khan
Dr. Nadia Younus
Dr. Masooma Talib
Dr. Iqra Anwar
Dr. Abeerah Zainub

Keywords

Prostate cancer, malignancies, worldwide, morbidity and mortality

Abstract

Prostate cancer remains one of the most prevalent malignancies affecting men worldwide, with a significant impact on morbidity and mortality.


Objectives: The main objective of the study is to find the Alpha-Methylacl-CoA Racemase (AMACR) expression in prostate cancer and its association with Gleason Grade and other histomorphological parameters.


Material and Methods: This retrospective observational study was conducted at Women Medical College, Abbottabad from January 2022 to February 2023. Data was collected from 110 patients diagnosed with prostate cancer. Clinical and pathological data including patient demographics, preoperative serum prostate-specific antigen (PSA) levels, imaging findings, biopsy results, and surgical pathology reports were collected from electronic medical records. Formalin-fixed paraffin-embedded (FFPE) tissue blocks from prostatectomy specimens or biopsy cores was retrieved from the pathology archives. Tissue sections (4-μm thick) were cut and subjected to immunohistochemical staining for AMACR expression using a commercially available antibody according to standard protocols. Positive and negative controls were included in each staining batch to ensure accuracy and reproducibility.


Results: Data were collected from 110 patients according to inclusion and exclusion criteria. Patients with a mean age of 65.4 years (± 7.2), presenting with preoperative PSA levels averaging 9.8 ng/mL (± 4.3). Most patients underwent MRI imaging (70%), while the remaining 30% underwent TRUS imaging. Biopsy results indicated a predominance of positive cases (105), with only 5 cases negative for prostate cancer. Gleason scores varied, with 30 cases classified as 6 (3+3), 50 as 7 (3+4), 20 as 7 (4+3), and 10 as 8-10. Patients with Gleason score 6 had a mean PSA level of 7.5 ng/mL (± 3.1) and a mean AMACR level of 0.45 (± 0.06). In contrast, patients with Gleason score 7 had a higher mean PSA level of 10.2 ng/mL (± 4.7) and a correspondingly higher mean AMACR level of 0.58 (± 0.09). Patients with more aggressive disease, classified as Gleason score 8-10, exhibited the highest mean PSA level of 12.4 ng/mL (± 5.6), accompanied by a higher mean AMACR level of 0.65 (± 0.11).

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References

1. Alinezhad, S., Väänänen, RM., Ochoa, N.T. et al. Global expression of AMACR transcripts predicts risk for prostate cancer – a systematic comparison of AMACR protein and mRNA expression in cancerous and noncancerous prostate. BMC Urol 16, 10 (2016). https://doi.org/10.1186/s12894-016-0128-8
2. Stephen, Norton, and Bhawana A. Badhe. "Diagnostic Utility of Immunohistochemical Markers Alpha Methyl Acyl CoA Racemase (AMACR) and Ets Related Gene (ERG) in Prostate Cancer." International Journal of Clinical and Experimental Pathology, vol. 15, no. 9, 2022, pp. 364-372, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9547992
3. Taheri, Diana, et al. "Diagnostic Utility of A-methylacyl COA Racemase in Prostate Cancer of the Iranian Population." Journal of Research in Medical Sciences : The Official Journal of Isfahan University of Medical Sciences, vol. 26, 2021, https://doi.org/10.4103/jrms.JRMS_311_19.
4. Lin, Po, et al. "Detection of Alpha-Methylacyl-CoA Racemase (AMACR), a Biomarker of Prostate Cancer, in Patient Blood Samples Using a Nanoparticle Electrochemical Biosensor." Biosensors, vol. 2, no. 4, 2012, pp. 377-387, https://doi.org/10.3390/bios2040377.
5. Gülhan, Ö., & Mahi, B. (2020). The role of AMACR, CD10, TMPRSS2-ERG, and p27 protein expression among different Gleason grades of prostatic adenocarcinoma on needle biopsy. Clinical Medicine Insights: Oncology, 14, 1179554920947322.
6. Sayed, R. M. S., El Shorbagy, G., & Shibel, P. E. E. (2023). Immunohistochemical Expression of Alpha-Methyl-Coa (AMACR) and ERG in Prostatic Adenocarcinoma and Prostatic Hyperplasia: A Comparative Study. Asian Pacific Journal of Cancer Prevention: APJCP, 24(8), 2861.
7. Stephen, N., & Badhe, B. A. (2022). Diagnostic utility of immunohistochemical markers alpha methyl acyl coA racemase (AMACR) and Ets related gene (ERG) in prostate cancer. International Journal of Clinical and Experimental Pathology, 15(9), 364.
8. Korček, M., Sekerešová, M., Makarevich, A. V., Gavurova, H., Olexikova, L., Pivko, J., & Barreto, L. (2020). Morphological and functional alterations of the prostate tissue during clinical progression in hormonally naïve, hormonally treated and castration resistant patients with metastatic prostate cancer. Oncology Letters, 20(5), 1-1.
9. Taheri, D., Roohani, E., Izadpanahi, M. H., Dolatkhah, S., Aghaaliakbari, F., Daneshpajouhnejad, P., ... & Rahbar, M. (2021). Diagnostic utility of a-methylacyl COA racemase in prostate cancer of the Iranian population. Journal of Research in Medical Sciences, 26(1), 46.
10. Okonkwo, D. I., Raphael, S., Anunobi, C. C., & Jibrin, P. G. (2021). Diagnostic utility of immunochemical technique using p63 and Alpha Methylacyl Coenzyme A Racemase (AMACR) in the diagnosis of core-needle biopsy of the prostate: Experience in a tertiary academic institution in Nigeria. Annals of Tropical Pathology, 12(1), 19.
11. Kiełb, P., Kowalczyk, K., Gurwin, A., Nowak, Ł., Krajewski, W., Sosnowski, R., ... & Małkiewicz, B. (2023). Novel histopathological biomarkers in prostate cancer: implications and perspectives. Biomedicines, 11(6), 1552.
12. Deepadevi, G. (2020). Immunohistochemical Expression of Estrogen Receptors Alpha and Beta in Prostate–As Proof of Concept for Developing Newer Therapeutic Options (Doctoral dissertation, Tirunelveli Medical College, Tirunelveli).
13. Dawoud, M. M., Aiad, H. A. S., Bahbah, A. M. N. H., & Shaban, M. I. (2021). Comparative study of immunohistochemical expression of ERG and MAGI2 in prostatic carcinoma. Annals of Diagnostic Pathology, 52, 151727.
14. Velickovic, L. J. (2024). Histopathological and Molecular Markers in the Assessment of Prostate Cancer Aggressivity. In Prostate Cancer: Advancements in the Pathogenesis, Diagnosis and Personalized Therapy (pp. 179-206). Cham: Springer Nature Switzerland.
15. Voulgari, O., Goutas, D., Pergaris, A., Belogiannis, K., Thymara, E., Kavantzas, N., & Lazaris, A. C. (2023). Correlations of PTEN and ERG immunoexpression in prostate carcinoma and lesions related to its natural history: Clinical perspectives. Current Issues in Molecular Biology, 45(4), 2767-2780.
16. Nili, F., Sadri, M., & Ameli, F. (2023). Utility of AMACR immunohistochemical staining in differentiating Arias-Stella reaction from clear cell carcinoma of ovary and endometrium. BMC cancer, 23(1), 332.
17. Čamdžić, N., Kuskunović-Vlahovljak, S., Dorić, M., Radović, S., Salčin, E. L., & Babić, M. (2021). Serum total prostate-specific antigen (tPSA): correlation with diagnosis and grading of prostate cancer in core needle biopsy. Medicinski Glasnik, 18(1).
18. Muthusamy, S., & Smith, S. C. (2024). Contemporary Diagnostic Reporting for Prostatic Adenocarcinoma: Morphologic Aspects, Molecular Correlates, and Management Perspectives. Advances in Anatomic Pathology, 10-1097.
19. Spinos, T., Georgiou, A., Voulgari, O., Goutas, D., Lazaris, A. C., Thymara, I., ... & Thomopoulou, G. E. (2023). Association Between ERG/PTEN Genes and Pathologic Parameters of Prostate Cancer With an Emphasis on Gleason Score: A Literature Review. Cancer Diagnosis & Prognosis, 3(3), 291.
20. Vetrone, L., Mei, R., Bianchi, L., Giunchi, F., Farolfi, A., Castellucci, P., ... & Fanti, S. (2023). Histology and PSMA Expression on Immunohistochemistry in High-Risk Prostate Cancer Patients: Comparison with 68Ga-PSMA PET/CT Features in Primary Staging. Cancers, 15(6), 1716.

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