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corticosterone and Urinary Bladder Neoplasms

corticosterone has been researched along with Urinary Bladder Neoplasms in 1 studies

Urinary Bladder Neoplasms: Tumors or cancer of the URINARY BLADDER.

Research Excerpts

ExcerptRelevanceReference
"Corticosterone and prednisone are suggested to have the potential of being harmless, in contrast to dexamethasone, without promoting cell proliferation or inhibiting cytotoxic activity of cisplatin, yet beneficial to bladder cancer patients via suppressing tumor invasion."7.80Differential regulation of bladder cancer growth by various glucocorticoids: corticosterone and prednisone inhibit cell invasion without promoting cell proliferation or reducing cisplatin cytotoxicity. ( Ishiguro, H; Kashiwagi, E; Kawahara, T; Li, Y; Miyamoto, H; Zheng, Y, 2014)
"Corticosterone and prednisone are suggested to have the potential of being harmless, in contrast to dexamethasone, without promoting cell proliferation or inhibiting cytotoxic activity of cisplatin, yet beneficial to bladder cancer patients via suppressing tumor invasion."3.80Differential regulation of bladder cancer growth by various glucocorticoids: corticosterone and prednisone inhibit cell invasion without promoting cell proliferation or reducing cisplatin cytotoxicity. ( Ishiguro, H; Kashiwagi, E; Kawahara, T; Li, Y; Miyamoto, H; Zheng, Y, 2014)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ishiguro, H1
Kawahara, T1
Zheng, Y1
Kashiwagi, E1
Li, Y1
Miyamoto, H1

Other Studies

1 other study available for corticosterone and Urinary Bladder Neoplasms

ArticleYear
Differential regulation of bladder cancer growth by various glucocorticoids: corticosterone and prednisone inhibit cell invasion without promoting cell proliferation or reducing cisplatin cytotoxicity.
    Cancer chemotherapy and pharmacology, 2014, Volume: 74, Issue:2

    Topics: Anti-Inflammatory Agents; Antineoplastic Agents; Apoptosis; Cell Movement; Cell Proliferation; Cispl

2014