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. 2023 Mar 7;13:1136227. doi: 10.3389/fonc.2023.1136227

Table 1.

Claudin (CLDN) protein functions, clinical significance, and the associated signaling.

Claudin type Main functions and clinical significance in PCa Signaling molecules involved Citatio-ns
claudin-1 • normal expression maintains the normal function of cells
• decreased expression promotes tumor cell invasion and metastasis
• ZEB1-regulated overexpression of ZIP4 reduces the expression of ZO-1 and claudin-1, leading to the phosphorylation of FAK and Paxillin, thus promoting PCa invasion and migration
• 5-HT1B, 5-HT1D, and eEF2K/MAPK-Erk pathway
(2833)
claudin-2 • decreased expression with an increase in tumor histological grade
• decreased expression in exocrine adenocarcinoma, cystic myxoma, and acinar cell carcinoma
• miR-222-3p and YAP (3336)
claudin-4 • differentially expressed in PCa
• effective inhibitor of the invasive and metastatic phenotype of PCa cells
• Ras/Raf/Erk pathway
• TGF-β and DEC1 siRNA
(3739)
claudin-5 • maintains cell polarity and cell barrier
• vascular endothelium, lymphatic vessels, and tumor interstitial blood vessel
• CD99 (4042)
claudin-6 • expression in embryonic stem cells
• no expression in normal adult tissues
• promotes chemotherapy resistance of MCF-7 cells
• regulates GSTP1
• promotes the chemotherapy resistance of MCF-7 cells via p53
(14, 4346)
claudin-7 • decrease in expression is parallel to the degree of tumor differentiation
• expressed in rapidly proliferating and dominant human PCa cell populations
• promotes tumorigenicity, accelerates tumor growth, and migration, and enhances drug resistance
• CIC-TEX
• EpCAM-CLDN-7 complex
(4749)
claudin-11 • expression is inhibited in the occurrence of nerve invasion
• Increased expression inhibits development of GC
• MALAT
• inhibition of miR-135b with lncRNA PCAT18, promotes the expression of claudin-11
(26, 50, 51)
claudin-12 • poor prognostic factor • SRSF1, LINC00857, and ZNF460 (52, 53)
claudin-18 • no specific staining detected in the normal pancreatic tissue, which was abnormally activated during the malignant transformation of pancreatic cells • PKCd, PKCe, and PKCa
• TPA and T/EBP/NKX2.1
• therapeutic target of Claudiximab (Zolbetuximab)
(5457)
claudin-23 • induced isolation of weakly invasive and migratory PCa cells (PC-1) • addition of a dissociation factor conditioned medium significantly reduced the expression of claudin-23 mRNA and protein in PC-1 cells (7, 58)

ZEB1, zinc finger E-box binding homeobox 1.