Figures & data
Table 1 Clinicopathological characteristics of the studied population (n=60)
Table 2 Correlation of CD133 and CD24 expression with clinicopathological parameters
Figure 1 Frequency of CD133+ and CD24+ tumor cells in bladder cancer. (A) Both CD133+ and CD24+ tumor cells were absent in low grade urothelial carcinoma, and (B) CD133+ and (C) CD24+ tumor cells were more frequent in non-papillary high grade urothelial carcinoma. (D) In non-urothelial bladder cancer, both CD133+ and CD24+ tumor cells were absent in well-differentiated squamous cell carcinomas. (E) CD133+ and (F) CD24+ tumor cells were more frequent as tumors grew less differentiated. (IHC, A, B, and D; ×200, C and E; ×400, F; ×100).
![Figure 1 Frequency of CD133+ and CD24+ tumor cells in bladder cancer. (A) Both CD133+ and CD24+ tumor cells were absent in low grade urothelial carcinoma, and (B) CD133+ and (C) CD24+ tumor cells were more frequent in non-papillary high grade urothelial carcinoma. (D) In non-urothelial bladder cancer, both CD133+ and CD24+ tumor cells were absent in well-differentiated squamous cell carcinomas. (E) CD133+ and (F) CD24+ tumor cells were more frequent as tumors grew less differentiated. (IHC, A, B, and D; ×200, C and E; ×400, F; ×100).](/cms/asset/803fe933-23c1-451d-9b80-002fe4c0e57b/dcmr_a_12186370_f0001_c.jpg)
Figure 2 Frequency of CD133+ and CD24+ tumor cells in muscle invasive bladder cancer. (A) In muscle invasive bladder cancers, (B) CD133+ cancer stem cells and (C) CD24+ cancer stem cells were frequent within the tumor cell population. (A, hematoxylin and eosin; ×200, B and C; IHC ×200; ×100, respectively).
![Figure 2 Frequency of CD133+ and CD24+ tumor cells in muscle invasive bladder cancer. (A) In muscle invasive bladder cancers, (B) CD133+ cancer stem cells and (C) CD24+ cancer stem cells were frequent within the tumor cell population. (A, hematoxylin and eosin; ×200, B and C; IHC ×200; ×100, respectively).](/cms/asset/52932400-03a7-4253-b80e-3b160d1aae5a/dcmr_a_12186370_f0002_c.jpg)
Figure 3 Expression of CD24 and CD133 in tumors with lymphovascular invasion. (A) The presence of CD24+ tumor stem cells exclusively correlated with lymphovascular invasion, regardless of (B) the presence of CD133+ tumor stem cells or (C) the absence of CD133+ tumor stem cells (IHC, A; ×200, B and C; ×400).
![Figure 3 Expression of CD24 and CD133 in tumors with lymphovascular invasion. (A) The presence of CD24+ tumor stem cells exclusively correlated with lymphovascular invasion, regardless of (B) the presence of CD133+ tumor stem cells or (C) the absence of CD133+ tumor stem cells (IHC, A; ×200, B and C; ×400).](/cms/asset/8e747d51-9787-48c3-8f2f-3ba764995f3d/dcmr_a_12186370_f0003_c.jpg)
Table 3 Correlation between CD133 and CD24 expression
Table 4 Association between CD133/CD24 phenotypes and other clinical characteristics
Data availability
Dataset reference: Farid, Rola M; Sammour, Sanaa; Shehab El-Din, Zeinab; Salman, Manal; Omran, Tag (2018), “Evaluation of CD133 and CD24 cancer stem cells and their different phenotypes in bladder carcinoma.”, Mendeley Data, v1http://dx.doi.org/10.17632/xj82cmj29g.1DOI