Literature DB >> 18480628

Clinical value of PTEN in patients with superficial bladder cancer.

Kyung Seok Han1, In Gab Jeong, Jae Young Joung, Seung Ok Yang, Jinsoo Chung, Ho Kyung Seo, Kyung Suk Kwon, Weon Seo Park, Kang Hyun Lee.   

Abstract

INTRODUCTION: Frequent mutations or deletions of PTEN (phosphatase and tensin homolog deleted on chromosome 10) are reported in bladder cancer, while there are few studies which evaluated PTEN as a clinical prognostic parameter of superficial bladder cancer. We prospectively evaluated PTEN expression in patients with superficial bladder cancer by immunohistochemical staining and defined the value of PTEN mutations in predicting tumor behavior of superficial bladder cancer.
MATERIALS AND METHODS: A total of 190 patients were enrolled in this study. All of the patients underwent transurethral resection of bladder tumor and had superficial tumors. All pathologic materials used in this study were obtained from transurethral resection of bladder tumor. Immunohistochemical stainings were performed. The immunohistochemical staining intensity was judged to be either normal or reduced compared with the PTEN protein expression of positive and negative controls. Disappearance of more than 50% stained cytoplasmic granules was defined as reduced PTEN expression.
RESULTS: The alteration of PTEN expression was significantly different according to tumor stage and grade (p = 0.03, p = 0.048), especially high in carcinoma in situ. However, PTEN expression was not significantly correlated with disease recurrence, progression and recurrence- or progression-free survival.
CONCLUSIONS: Reduced PTEN expression relates to aggressiveness of bladder tumors but seems not to have enough specificity for clinical use in the management of superficial bladder cancer. 2008 S. Karger AG, Basel

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Year:  2008        PMID: 18480628     DOI: 10.1159/000127338

Source DB:  PubMed          Journal:  Urol Int        ISSN: 0042-1138            Impact factor:   2.089


  5 in total

1.  The role of PTEN tumor suppressor pathway staining in carcinoma in situ of the bladder.

Authors:  John P Sfakianos; Lan Lin Gellert; Alexandra Maschino; Geoffrey T Gotto; Philip H Kim; Hikmat Al-Ahmadie; Bernard H Bochner
Journal:  Urol Oncol       Date:  2014-05-16       Impact factor: 3.498

2.  Single-Cell Analyses of a Novel Mouse Urothelial Carcinoma Model Reveal a Role of Tumor-Associated Macrophages in Response to Anti-PD-1 Therapy.

Authors:  Dongbo Xu; Li Wang; Kyle Wieczorek; Yali Zhang; Zinian Wang; Jianmin Wang; Bo Xu; Prashant K Singh; Yanqing Wang; Xiaojing Zhang; Yue Wu; Gary J Smith; Kristopher Attwood; Yuesheng Zhang; David W Goodrich; Qiang Li
Journal:  Cancers (Basel)       Date:  2022-05-19       Impact factor: 6.575

3.  Phosphatidylinositol 3'-kinase, mTOR, and glycogen synthase kinase-3β mediated regulation of p21 in human urothelial carcinoma cells.

Authors:  Nicole L Yohn; Caitlyn N Bingaman; Ashley L DuMont; Lina I Yoo
Journal:  BMC Urol       Date:  2011-08-24       Impact factor: 2.264

4.  Effect of PTEN Gene Mutations and Environmental Risk Factors on the Progression and Prognosis of Bladder Cancer.

Authors:  Rahil Mashhadi; Gholamreza Pourmand; Abdolrasou Mehrsai; Saeed Pakdel; Hossein Dialameh; Ayat Ahmadi; Sepehr Salem; Elaheh Salimi; Ramina Mahboubi
Journal:  Iran J Public Health       Date:  2014-01       Impact factor: 1.429

Review 5.  Predictive Markers for the Recurrence of Nonmuscle Invasive Bladder Cancer Treated with Intravesical Therapy.

Authors:  Yasuyoshi Miyata; Hideki Sakai
Journal:  Dis Markers       Date:  2015-11-23       Impact factor: 3.434

  5 in total

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