Major histocompatibility complex molecules (HLA), the co-stimulatory molecule B7 and the intercellular adhesion molecule 1 (ICAM-1) are key molecules involved in T cell-mediated immune surveillance. We aimed at assessing the expression pattern of these immunoregulatory molecules on primary esophagea
Prognostic significance of β-microseminoprotein mRNA expression in prostate cancer
✍ Scribed by Hideki Sakai; Toshifumi Tsurusaki; Shigeru Kanda; Takehiko Koji; Jim W. Xuan; Yutaka Saito
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 220 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0270-4137
No coin nor oath required. For personal study only.
✦ Synopsis
BACKGROUND. Human -microseminoprotein (-MSP or PSP94) is a small protein secreted by prostatic epithelial cells. We recently reported the presence of low levels of -MSP mRNA expression and protein in most prostate cancer tissues. METHODS. -MSP and mRNA expression was examined by in situ hybridization in biopsy specimens obtained from 92 patients with prostate cancer. All tissue specimens were obtained by needle biopsies prior to treatment. All patients subsequently received endocrine therapy. To estimate the influence of -MSP mRNA expression and three possible prognostic factors, i.e., patient age, clinical stage, and Gleason score, on time to progression under endocrine therapy, univariate and multivariate analyses were performed using Cox's proportional hazards regression model. RESULTS. Multivariate survival analysis showed that clinical stage was the strongest prognostic factor (P =0.006) and that -MSP mRNA expression was the second strongest factor (P = 0.038) in 92 patients with stage B-D disease. Analysis of only 51 patients with stage D disease showed that -MSP mRNA expression was the only significant prognostic indicator for progression under endocrine therapy (P = 0.003). CONCLUSIONS. The presence of cells that express the -MSP transcript may be a novel indicator of potentially aggressive prostate cancer.
📜 SIMILAR VOLUMES
This study has evaluated the expression of the cyclin-dependent kinase inhibitor p27 Kip1 in 89 colorectal cancers (CRCs) using immunohistochemistry and has related p27 levels to clinico-pathological characteristics, tumour cell proliferation, and the expression of other G1-S transition regulatory p
BACKGROUND. p21(waf1/cip1) protein is a cyclin-dependent kinase inhibitor able to arrest the cell cycle at the G1 phase by inhibiting DNA replication. The expression of p21(waf1/cip1) and its prognostic value in prostate cancer are largely unexplored. METHODS. We used immunohistochemistry to analyze
It is well established that the activation of proto-oncogenes could trigger uncontrolled cell growth and cancer development. Although this correlation has already been evidenced in several human tumors, no conclusive studies have related oncogene activation with the development of prostatic neoplasi