Abstract | BACKGROUND/AIM: PATIENTS AND METHODS: In this study, WWC1 immunoreactivity was investigated in 152 non-metastatic UTUC samples. The relationships between WWC1 expression and grade, pT stage, proliferative index (using an antibody to Ki-67), and the immunohistochemical expression of matrix metalloproteinase (MMP)-2 and -9 were evaluated. RESULTS: WWC1 expression was negatively associated with tumor grade and pT stage (p<0.001). Positive expression of WWC1 was a better predictor of the UTUC recurrence and subsequent metastasis, and the multivariate analysis showed that WWC1 expression was a significant predictor of subsequent metastasis (hazard ratio=0.29, p=0.020). WWC1 expression inversely correlated with the proliferative index (odds ratio=2.59, p=0.023) and expression of MMP9 (odds ratio=2.19, p=0.040) but not with MMP2 expression, by multivariate analyses. CONCLUSION: WWC1 expression was negatively associated with malignant aggressiveness via the suppression of cancer cell proliferation and MMP9 expression in patients with UTUC. This suggests WWC1 to be a useful predictor and novel therapeutic target in patients with UTUC.
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Authors | Hiroki Kurata, Kensuke Mitsunari, Tsubasa Kondo, Masahito Masato, Hidenori Ito, Yuta Mukae, Yuichiro Nakamura, Tomohiro Matsuo, Kojiro Ohba, Yasushi Mochizuki, Hideki Sakai, Yasuyoshi Miyata |
Journal | Anticancer research
(Anticancer Res)
Vol. 42
Issue 5
Pg. 2311-2317
(May 2022)
ISSN: 1791-7530 [Electronic] Greece |
PMID | 35489728
(Publication Type: Journal Article)
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Copyright | Copyright © 2022 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved. |
Chemical References |
- Intracellular Signaling Peptides and Proteins
- WWC1 protein, human
- Matrix Metalloproteinase 9
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Topics |
- Carcinoma, Transitional Cell
(pathology)
- Female
- Humans
- Intracellular Signaling Peptides and Proteins
- Kidney Neoplasms
(pathology)
- Kidney Pelvis
(pathology)
- Male
- Matrix Metalloproteinase 9
- Prognosis
- Ureteral Neoplasms
(pathology)
- Urologic Neoplasms
(pathology)
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