Relationship Between LSD1 Expression and E-cadherin Expression in Prostate Cancer
Overview
Affiliations
Purpose: To investigate the relationship between the expression of LSD1 and E-cadherin in prostate cancer and their prognostic significance.
Methods: The expression of LSD1 and E-cadherin in prostate cancer was detected using immunohistochemistry, and the relationship between the expressions of these two molecules was analyzed by correlation analysis. Furthermore, LNCap cell line was treated with Pargyline (an inhibitor of LSD1), and Western blot was used to analyze LSD1 and E-cadherin expression.
Results: LSD1 expression increased significantly in prostate cancer specimens compared with benign prostatic hyperplasia (P < 0.05). Further analysis testified that LSD1 expression was positively correlated with higher Gleason Score, distant metastases, and poor prognosis (P < 0.05). Nevertheless, E-cadherin expression decreased significantly in prostate cancer specimens compared with benign prostatic hyperplasia (P < 0.05) and was negatively correlated with higher Gleason Score, distant metastases (P < 0.05). Correlation analysis revealed that LSD1 expression was negatively correlated with E-cadherin expression in prostate cancer (rs = -0.486, P = 0.001). Positive LSD1 expression and negative E-cadherin expression were significantly correlated with high 2-year progression (occurrence of castration-resistant prostate cancer) rate and low 5-year survival rate (P < 0.05). Moreover, Pargyline inhibited activity of LSD1 and up-regulated E-cadherin expression.
Conclusion: High LSD1 expression combined with low E-cadherin expression might be predictors of prostate cancer progression and metastasis. Inhibition of LSD1 may be a potential therapeutic target for prevention of prostate cancer.
Ahmed K, Sheikh A, Fatima S, Ghulam T, Haider G, Abbas F Sci Rep. 2024; 14(1):10315.
PMID: 38705879 PMC: 11070424. DOI: 10.1038/s41598-024-60538-0.
LSD1-Based Reversible Inhibitors Virtual Screening and Binding Mechanism Computational Study.
Yin Z, Liu S, Yang X, Chen M, Du J, Liu H Molecules. 2023; 28(14).
PMID: 37513188 PMC: 10383809. DOI: 10.3390/molecules28145315.
Yan G, Zhang H, Li Y, Miao G, Liu X, Lv Q Invest New Drugs. 2023; 41(1):134-141.
PMID: 36692618 DOI: 10.1007/s10637-023-01330-1.
Xu Y, Fan B, Gao Y, Chen Y, Han D, Lu J Molecules. 2022; 27(23).
PMID: 36500451 PMC: 9739212. DOI: 10.3390/molecules27238358.
Heterocycle-containing tranylcypromine derivatives endowed with high anti-LSD1 activity.
Fioravanti R, Rodriguez V, Caroli J, Chianese U, Benedetti R, Di Bello E J Enzyme Inhib Med Chem. 2022; 37(1):973-985.
PMID: 35317680 PMC: 8942502. DOI: 10.1080/14756366.2022.2052869.