Tissue Profile of CDK4 and STAT3 as Possible Innovative Therapeutic Targets in Urinary Bladder Cancer

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorAboushousha, T
dc.contributor.authorHammam, O
dc.contributor.authorAref, A
dc.contributor.authorKamel, A
dc.contributor.authorBadawy, M
dc.contributor.authorAbdel Hamid, A
dc.date.accessioned2020-03-08T08:04:29Z
dc.date.available2020-03-08T08:04:29Z
dc.date.issued02/01/2020
dc.description.abstractBladder cancer represents a global health problem. It ranks ninth in worldwide cancer incidence. In Egypt, carcinoma of the bladder is the most prevalent cancer, Bladder cancer has the highest recurrence rate of any malignancy. Certainly, suitable molecular diagnostic markers are required to improve the early detection of bladder cancer and then to prolong survival of patients. The present study was aimed to explore the expression of CDk4 and STAT3 in bladder cancer tissues as prospective for target therapy. Our studied groups showed higher values of CDK4 and STAT3 expression in malignant tissues (SCC andUC collectively) compared to cystitis, however, significantly higher values of CDK4 and STAT3 expression were detected in UC group compared to SCC group. Urothelial carcinomas with papillary patterns showed lower parameters of CDK4 and STAT3 expression compared to the non-papillary variant, with significant differences. Higher grades of UC showed significantly higher parameters of CDK4 and STAT3 expression compared to low grade ones. Muscle invasion increases the level of CDK4 and STAT3 expression parameters, compared to non-muscle invasive UC. Conclusion: Our results showed a good correlation of the expression patterns of both the cell cycle (CDK4) and inflammatory (STAT3) markers studied and might be helpful for suggesting more selective agents in the therapeutic scenario of bladder cancer in the near future. Potential biomarkers such as CDK4 andSTAT3 may be targets for molecular based therapeutic strategies in the prevention or management of bladder cancer. Future studies should explore molecular mechanisms of these proteins to define their roles in tumorigenesisen_US
dc.identifier.doihttps://doi.org/10.31557/APJCP.2020.21.2.547
dc.identifier.issn2476762X
dc.identifier.otherhttps://doi.org/10.31557/APJCP.2020.21.2.547
dc.identifier.urihttps://t.ly/1k0B8
dc.language.isoen_USen_US
dc.publisherNLM (Medline)en_US
dc.relation.ispartofseriesAsian Pacific journal of cancer prevention : APJCP;Volume 21, Issue 2, 1 February 2020, Pages 547-554
dc.subjectuniversity of STAT3en_US
dc.subjectCDK4en_US
dc.subjectbladder canceren_US
dc.titleTissue Profile of CDK4 and STAT3 as Possible Innovative Therapeutic Targets in Urinary Bladder Canceren_US
dc.typeArticleen_US

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