Parathyroid hormone related-protein (PTHrP) in tissues with poor prognosis in prostate cancer patients

Author:

Zhao Yan123ORCID,Lu Sheng-Ming4,Zhong Bing5,Wang Gong-Cheng5,Jia Rui-Peng6,Wang Qian1,Long Jian-Hua7

Affiliation:

1. Department of Urology, Xuzhou Cancer Hospital, Affiliated Hospital of Jiangsu University, Xuzhou, Jiangsu, China

2. Department of Urology, Xuzhou New Health Geriatric Disease Hospital, Xuzhou, Jiangsu, China

3. Department of Urology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China

4. Department of Urology, Subei People’s Hospital, Yangzhou, Jiangsu, China

5. Department of Urology, The First People’s Hospital of Huaian, Affiliated with Nanjing Medical University, Huaian, Jiangsu, China

6. Department of Urology, Nanjing First Hospital Affiliated to Nanjing Medical University, Nanjing, Jiangsu, China

7. Department of Urology, The Second Affiliated Hospital of the University of South China, Hengyang, Hunan, China.

Abstract

Background: Parathyroid hormone-related peptide (PTHrP) is known to have a pivotal role in the progression of various solid tumors, among which prostate cancer stands out. However, the extent of PTHrP expression and its clinical implications in prostate cancer patients remain shrouded in obscurity. The primary objective of this research endeavor was to shed light on the relevance of PTHrP in the context of prostate cancer patients and to uncover the potential underlying mechanisms. Methods: The expression of PTHrP, E-cadherin, and vimentin in tumor tissues of 88 prostate cancer patients was evaluated by immunohistochemical technique. Subsequently, the associations between PTHrP and clinicopathological parameters and prognosis of patients with prostate cancer were analyzed. Results: Immunohistochemical analysis showed that the expression rates of PTHrP, E-cadherin, and vimentin in prostate cancer tissues were 95.5%, 88.6%, and 84.1%, respectively. Patients with a high level of PTHrP had a decreased expression of E-cadherin (P = .013) and an increased expression of vimentin (P = .010) compared with patients with a low level of PTHrP. Besides, the high expression of PTHrP was significantly correlated with a higher level of initial prostate-specific antigen (P = .026), positive lymph node metastasis (P = .010), osseous metastasis (P = .004), and Gleason score (P = .026). Moreover, patients with a high level of PTHrP had shorter progression-free survival (P = .002) than patients with a low level of PTHrP. Conclusion: The present study indicates that PTHrP is associated with risk factors of poor outcomes in prostate cancer, while epithelial-mesenchymal transition may be involved in this process.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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