Page 38 - MI-1-1
P. 38
Microbes & Immunity The feature of bladder cancer stem cells
Figure 2. The signaling pathways driving the self-renewal of bladder cancer stem cells.
Figure 3. Hedgehog pathway in bladder cancer stem cells. GLANT1 mediates O-linked glycosylation of Sonic Hedgehog (SHH), leading to the activation
of SHH. This activation terminates the inhibition of PTCH1 on Smoothened (SMO). Subsequently, SMO activates GLI1, which then translocates to the
nucleus and initiates the transcriptional activation of the SHH target gene.
3.3.2. WNT pathway in tumors, the WNT pathway emerges as an effective target
The WNT signaling pathway, highly conserved throughout for cancer therapy.
evolution, is involved in numerous biological processes. In 2009, researchers led by Xiaobing He at Johns Hopkins
Within stem cells, the WNT signaling pathway plays a University in the United States identified highly expressed
+
crucial role in maintaining the delicate balance between factors related to the WNT signaling pathway in 67LR /
+
-
differentiation and proliferation. WNT ligands bind to CEACAM6 /CK17 BCSCs through Kyoto Encyclopedia
the co-receptor lipoprotein receptor-related protein 5 or of Genes and Genomes (KEGG) analysis. Transcriptomic
6 (LRP5/6) in conjunction with the seven-transmembrane analysis revealed significant overexpression of WNT-4,
receptor Frizzled (FZD) (Figure 4). This interaction WNT-6, WNT-10A, FZD6, β-catenin, and WNT pathway
enhances the stability of WNT effectors and transcriptional target genes such as MYC and matrix metalloproteinase
co-activator β-catenin. Subsequently, β-catenin 7 (MMP7) in 67LR high BCSCs. These results suggest the
41
translocates into the cell nucleus, regulating the expression potential role of the WNT pathway in regulating BC tumor
levels of WNT target genes and thereby conferring self- growth. However, the direct correlation between the self-
-
+
+
renewal capacity to cells. Given its frequent dysregulation renewal ability of 67LR /CEACAM6 /CK17 BCSCs
Volume 1 Issue 1 (2024) 32 doi: 10.36922/mi.2377

