Submitted Successfully!
To reward your contribution, here is a gift for you: A free trial for our video production service.
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Version Summary Created by Modification Content Size Created at Operation
1
Hiroki Kuniyasu
 -- 2242 2023-05-24 12:03:38 |
2 Reference format revised.
Lindsay Dong
 Meta information modification 2242 2023-05-25 02:52:31 |

Video Upload Options

We provide professional Video Production Services to translate complex research into visually appealing presentations. Would you like to try it?
No, upload directly Yes

Confirm

Are you sure to Delete?
Yes No
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Fujiwara-Tani, R.; Mori, S.; Ogata, R.; Sasaki, R.; Ikemoto, A.; Kishi, S.; Kondoh, M.; Kuniyasu, H. Claudin-4 as Molecular Target for Epithelial Cancer Therapy. Encyclopedia. Available online: https://encyclopedia.pub/entry/44768 (accessed on 26 December 2024).
Fujiwara-Tani R, Mori S, Ogata R, Sasaki R, Ikemoto A, Kishi S, et al. Claudin-4 as Molecular Target for Epithelial Cancer Therapy. Encyclopedia. Available at: https://encyclopedia.pub/entry/44768. Accessed December 26, 2024.
Fujiwara-Tani, Rina, Shiori Mori, Ruiko Ogata, Rika Sasaki, Ayaka Ikemoto, Shingo Kishi, Masuo Kondoh, Hiroki Kuniyasu. "Claudin-4 as Molecular Target for Epithelial Cancer Therapy" Encyclopedia, https://encyclopedia.pub/entry/44768 (accessed December 26, 2024).
Fujiwara-Tani, R., Mori, S., Ogata, R., Sasaki, R., Ikemoto, A., Kishi, S., Kondoh, M., & Kuniyasu, H. (2023, May 24). Claudin-4 as Molecular Target for Epithelial Cancer Therapy. In Encyclopedia. https://encyclopedia.pub/entry/44768
Fujiwara-Tani, Rina, et al. "Claudin-4 as Molecular Target for Epithelial Cancer Therapy." Encyclopedia. Web. 24 May, 2023.
Claudin-4 as Molecular Target for Epithelial Cancer Therapy
Edit
This entry is adapted from the peer-reviewed paper 10.3390/ijms24065494

Claudin-4 (CLDN4) is a key component of tight junctions (TJs) in epithelial cells. CLDN4 is overexpressed in many epithelial malignancies and correlates with cancer progression. Changes in CLDN4 expression have been associated with epigenetic factors (such as hypomethylation of promoter DNA), inflammation associated with infection and cytokines, and growth factor signaling. CLDN4 helps to maintain the tumor microenvironment by forming TJs and acts as a barrier to the entry of anticancer drugs into tumors. Decreased expression of CLDN4 is a potential marker of epithelial-mesenchymal transition (EMT), and decreased epithelial differentiation due to reduced CLDN4 activity is involved in EMT induction. Non-TJ CLDN4 also activates integrin beta 1 and YAP to promote proliferation, EMT, and stemness. These roles in cancer have led to investigations of molecular therapies targeting CLDN4 using anti-CLDN4 extracellular domain antibodies, gene knockdown, clostridium perfringens enterotoxin (CPE), and C-terminus domain of CPE (C-CPE), which have demonstrated the experimental efficacy of this approach. 

claudin-4 cancer molecular target tight junction non-tight junction claudin

1. Introduction

Tight junctions (TJs) are multiprotein complexes present at the tip of the lateral membrane of polarized epithelial and endothelial cells [1]. The main function of these structures is to mediate adhesion and polarity between cells. Therefore, it is believed that the impairment of TJs and the concomitant loss of cell-to-cell adhesion are necessary for the early stages of cancer invasion and metastasis. However, it is becoming increasingly clear that TJ proteins such as claudins play important roles not only in adhesion but also in the activation of intracellular signaling, which contributes to tumor progression and metastasis. Claudin (CLDN) is a cell-to-cell adhesion component of the tight junctions and forms a protein family with 27 highly homologous members [2][3]. CLDN4 is the major CLDN involved in TJs in epithelial cells, such as those in the intestines and lungs, and is associated with many epithelial malignancies [4][5].

2. CLDN4 Expression and Regulation in Cancer

Overexpression of CLDN4 has been reported in various cancers, such as gastric cancer [6][7][8], pancreatic cancer [9][10][11], colorectal cancer [12][13], breast cancer [14][15] (especially triple-negative breast cancer [16][17]), oral squamous cell carcinoma [18], ovarian cancer [19], bladder cancer [20][21], non-small cell lung cancer [22], and cholangiocarcinoma [23]. In all of these cases, CLDN4 expression correlated with disease progression and poor prognosis. CLDN4 is also overexpressed in thyroid cancer [24] and prostate cancer [25][26]; however, in these cancers, decreased expression correlated with poor prognosis.

2.1. Epigenetics

Epigenetic alterations play a major role in carcinogenesis and cancer progression in various malignancies [27][28][29]. Changes in DNA methylation, histone modifications, chromatin remodeling, and microRNAs are considered useful indicators of cancer development and progression [27], and epigenetic changes in the regulation of CLDN4 expression have recently been reported. Hypermethylation of CpG islands in the CLDN4 promoter region reduces CLDN4 expression in gastric, bladder, and colon cancers [30][31][32]. In contrast, CLDN4 hypomethylation and CLDN4 overexpression have been reported in gastric, breast, ovarian, and bladder cancers [21][33][34][35].
Epigenetic regulation of CLDN expression has also been reported for CLDN1 [32][36][37], CLDN2 [38], CLDN3 [30][39][40], CLDN6 and CLDN9 [41], CLDN7 [42], and CLDN11 [43]. Several studies have also indicated the involvement of microRNAs in the regulation of CLDN4 expression. CLDN4 is a target gene of miR497-3p and the long non-coding RNA ELFN1-AS1, which promotes CLDN4 expression by sponging miR497-3p [44].

2.2. Inflammatory Processes

In gastric cancer, CLDN4 expression is elevated in Helicobacter pylori-positive cases [8]. Here, CLDN4 expression is upregulated by CDX2, leading to an intestinal phenotype induced by H. pylori infection [45]. CLDN4 is downregulated by inflammatory cytokines such as TNFα and HMGB1 [13][46]. In rheumatoid arthritis, blood IL-4, -5, -6, and -13 levels are elevated, while the levels of CLDN4, 7, 12, and 15, as well as ZO-1, are decreased [47]. IL-18 represses the expression of CLDN1, 3, 4, and 12 [48].

2.3. Growth Factors

Smad signaling triggered by TGF-β induces CLDN4 promoter activity via c-Jun, enhancing CLDN4 expression [49]. In mouse intestinal epithelium, knockdown of smad4 has been shown to reduce the expression of CLDN3 and 4, but increase that of CLDN2 and 8, resulting in increased intestinal permeability [50]. In glioblastoma, TGFβ promotes CLDN4 expression and enhances invasive ability [51]. Other signaling pathways that affect CLDN4 expression include PKCα [52], twist [53], ERK1/2 [54], p38MAPK [55], HIF1α [56], and hedgehog [57].

3. The Function of CLDN4 in Cancer

3.1. Carcinogenesis

CLDN4 overexpression has been detected in several cancers, including lung, gastric, colorectal, endometrial, uterine cervical, and ovarian epithelial cancers. In these cancers, precancerous lesions, atypical adenomatous hyperplasia, gastric dysplasia, sessile serrated adenoma/polyp with dysplasia (SSA/P-D), atypical endometrial hyperplasia, cervical intraepithelial neoplasia (CIN), and borderline malignant lesions display increased expression and/or abnormal distribution of CLDN4 [58][59][60][61][62][63].

3.2. Barrier Function and Maintenance of Intratumoral Microenvironment

CLDN4 is a major structural protein of epithelial TJs in intestines and lungs and is involved in epithelial differentiation, polarity maintenance, and substance trafficking [64][65]. In normal epithelial tissue, TJs act as barriers or gates that separate the outside from the inside of the body and restrict material transport; however, in tumor tissue, the polarity of the cells and tissues is ambiguous. Thus, in CLDN4-overexpressing epithelial malignancies, the barrier function of TJs serves to maintain the tumor microenvironment and retain tumor-secreted growth factors to promote the malignant cancer phenotype (Figure 1) [8][11][13][16][20].
/media/item_content/202305/646eb061405ebijms-24-05494-g001.png
Figure 1. Barrier function of TJs: CLDN4, which is overexpressed in epithelial malignancies, separates the intratumoral microenvironment from the tumor exterior by forming TJs. As a result, growth factors (such as EGF and VEGF) and metabolites (such as lactate) accumulate in the intratumoral microenvironment, resulting in amplification of their effects. This promotes increased tumor grade and suppression of immune cell infiltration into the tumor. TJs also inhibit the penetration of anticancer drugs from the tumor exterior into the microenvironment and enhance resistance to anticancer drugs. CLDN4, claudin-4; TJ, tight junction; EGF, epidermal growth factor; VEGF, vascular endothelial growth factor.
In assessing the barrier action of TJ CLDN4, it is necessary to consider its involvement in transport in normal TJs. TJ controls material transport through the paracellular and transcellular routes. Utilization of these pathways is affected by the ratio of ionized and unionized species (which depends on the pKa of the drug, the size of the molecules, and the pH of the solution), the intrinsic partition coefficient of the drug, and the size of the molecule and its charge [66]. 

3.3. Apoptosis

Several studies have suggested that CLDN4 expression is involved in promoting cancer cell viability. CLDN4 suppresses cell death caused by apoptosis [15][67] and endoplasmic reticulum stress [68]. It is believed that non-TJ CLDN4 activates integrin β1 as a binding partner and suppresses apoptosis via FAK signaling [8][21]. In addition, CLDN1 [69][70] increases resistance to anoikis, whereas CLDN6 decreases it [71]. However, the effect of CLDN4 on anoikis is still unclear.

3.4. Stemness and EMT

In EMT, epithelial cells lose epithelial differentiation and transition to mesenchyme, which involves background dedifferentiation from the epithelium and enhanced stemness [72]. It has become clear that cancer stemness is the basis of tumorigenicity, self-renewal, and differentiation, as well as tumor heterogeneity, metastasis, and treatment resistance [73]. Decreased expression of CLDN4, an epithelial marker in tumors, reflects EMT and is also associated with metastasis [74][75]. EMT correlates with hypermethylation of the CLDN4 promoter, which causes downregulation of CLDN4 [76], while the transcription factor Bach1 directly suppresses the expression of CLDN4 and E-cadherin to induce EMT [77]. Thus, CLDN4 expression is a marker of epithelial traits, and its decrease is thought to be suggestive of EMT. However, Ma et al. reported that repression of CLDN4 expression suppresses invasion and metastasis in breast cancer cell lines [15].

4. Non-TJ Functions of CLDN4

4.1. Non-TJ Plasma Membrane CLDN4

CLDN4 is overexpressed in bladder cancer due to promoter DNA hypomethylation [21]. Further demethylation via aza-2′-deoxycytidine (AZA) treatment induces expression of CLDN4 to levels above that necessary for TJ function. This is accompanied by the formation of CLDN4 monomers that do not incorporate into TJs [21]. This process is considered to be one of the mechanisms responsible for generating non-TJ CLDN4.

4.2. Cytoplasmic CLDN4

CLDN4 can also be taken from TJs to form a non-plasma membrane (cytoplasmic) CLDN4. Studies have demonstrated that the C-terminus domain of Clostridium perfringens enterotoxin (CPE) binds to the second extracellular loop of CLDN4, disrupting homotypic claudin binding, impairing TJs, and leading to diarrhea [78]. As a result, CLDN4 is released from TJs and translocated into the cytoplasm [13][18].

4.3. Function of Non-TJ CLDN4

4.3.1. Integrin β1 Activation

Integrin β1 activates FAK and induces the expression of stem cell-related genes such as Oct4, Sox2, and Nanog through Notch signaling [79][80]. Non-TJ CLDN4 binds to integrin β1 and enhances stemness, anti-apoptotic effects, drug resistance, and metastatic capacity of cancer cells (Figure 2A) [8][21]. In poorly differentiated gastric cancer, TJ formation is reduced, but EMT is mediated by non-TJ CLDN4 [8]. CLDN7, like CLDN4, also binds to integrin β1, leading to downstream FAK phosphorylation [81][82]. CLDN4 exhibits approximately 40% of the affinity of CLDN7 for integrin β1 [8].
Ijms 24 05494 g002 550
Figure 2. The function of non-TJ CLDN4. (A) CLDN4 monomer that does not form TJs is a binding partner for integrin β1 expressed in neighboring tumor cells, activates FAK, and promotes expression of stemness-associated genes. (B) CLDN4 translocates into the cytoplasm from TJs disrupted by CPE and forms a stable complex with TAZ, MST, LATS, and ZO1, but YAP is released from the complex and translocates into the nucleus with ZO2 to induce expression of YAP target genes, leading to proliferation and EMT. (C) EphA2 activated by Ephrin A1 expressed on the surface of neighboring cells phosphorylates CLDN4 and releases it from TJs. The released CLDN4 is translocated into the nucleus with YAP. CLDN4, claudin-4; TJ, tight junction; CPE, Clostridium perfringens enterotoxin; TAZ, tafazzin; YAP, yes-associated protein; ZO, zonula occludens; MST, mammalian Ste20-like kinase; LATS, large tumor suppressor kinase; Eph A2, ephrin type-A receptor 2; FAK, focal adhesion kinase; EMT, epithelial-mesenchymal transition.

4.3.2. YAP Activation

Cytoplasmic CLDN4 is also involved in YAP activation [18][60][83]. CLDN4 translocated to the cytoplasm by C. perfringens CPE in the intestinal flora forms a stable complex involving TAZ, LATS, MST of HIPPO inhibitory system, and ZO-1. This sequestration of the YAP co-activator TAZ leaves YAP free to bind to ZO-2 and translocate to the nucleus, where it promotes the expression of target genes such as cyclin E and snail, stimulating proliferation and inducing EMT (Figure 2B) [60]. As a result, it promotes carcinogenesis of SSA/P-D, a colonic precancerous lesion, and is associated with BRAF mutations in colorectal cancer [60]. As mentioned earlier, in renal cell carcinoma, EphA2/Ephrin A1 and PKCε translocate CLDN4 into the nucleus, with YAP bound and co-translocated alongside CLDN4. As a result, YAP is activated and increases the malignancy of cancer cells (Figure 2C) [83]. YAP activation by CLDN also occurs with CLDN6 and CLDN18. Several factors are involved in YAP nuclear translocation and activation, including the inhibition of YAP phosphorylation by LATS [84], CLDN6-ZO2-YAP interactions [85], and the binding of CLDN18 with YAP [86], which together lead to a poor prognosis in gastric cancer [87].

4.3.3. Activation of AKT

CLDN4 has also been linked to AKT signaling. CLDN4 has been shown to induce PIK3R3 and MAP2K2 mRNA expression and activate AKT and ERK1/2 in acute myeloid leukemia cells [88]. This results in accelerated proliferation and poor prognosis for this disease. Another study indicated that SPTBN2 cooperates with CLDN4 to stimulate PI3K/AKT activation [89]. Conversely, there is also a report that silencing CLDN4 activates AKT [90]. CLDN4 limits the activity of β-catenin and PI3K and inhibits the phosphorylation and activity of EphA2 by AKT [91].

5. Targeting CLDN4

5.1. Antibodies

To target CLDN4 with antibodies, it is essential to generate an antibody against its extracellular domain, but it is difficult to generate a single CLDN-specific antibody due to the high homology among CLDN family members [92]. The antibodies reported to be established thus far include monoclonal antibodies that recognize the extracellular loops of both CLDN3 and CLDN4 and their antitumor effects have been confirmed both in vitro and in vivo [93][94]. Suzuki et al. generated a monoclonal antibody (KM3900) that recognizes CLDN4 extracellular loop 2 and induces antibody-dependent cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC) in vitro and inhibited the growth of pancreatic and ovarian tumors in SCID mice in vivo [95].

5.2. Knockdown

Knocking down CLDN4 in gastric cancer and bladder cancer results in a mild decrease in transepithelial electrical resistance (TER), an indicator of TJ function [8][21]. For this reason, CLDN4 knockdown only provides limited disruption of the microenvironment and the promotion of anticancer drug permeability by impairing TJs. One possible reason for this is that the knockdown of a single CLDN may result in other CLDNs maintaining TJ function in its place. However, CLDN4 knockdown does reduce non-TJ CLDN4 and thus inhibits stemness [21].

5.3. CPE and C-Terminus Domain of CPE (C-CPE)

CPE recognizes specific amino acid sequences in the first and second extracellular loops of CLDN4 and CLDN3 and docks via a pocket of the domain at the C-terminus to disrupt TJs. Furthermore, it perforates the plasma membrane to cause cell death due to the intracellular influx of calcium [78][96]. Therefore, CPE exhibits cytotoxicity against cancer cells expressing CLDN4. The antitumor effect of CPE has been demonstrated by experiments in prostate cancer [97][98], non-small cell lung cancer [22], pancreatic cancer [10], gastric cancer [99], and ovarian cancer [100][101].

5.4. Peptide

Attempts have also been made to produce specific peptides as CLDN binding agents. Hicks et al. showed that a small peptide that mimics the DFYNP sequence in the second extracellular loop of CLDN4 impairs CLDN4, leading to the induction of apoptosis and suppression of tumor growth [67]. In light of these promising data, further progress is expected in peptide drug discovery to target CLDN4.

5.5. Delivery of Anti-CLDN4 Drugs

In many cases, CLDN4-targeting drugs such as those described above reach the tumor through blood administration. At this time, the formation of tumor blood vessels is important for the effective delivery of molecular-targeted drugs. As mentioned above, the barrier action of CLDN4 leads to the accumulation of angiogenic factors within the tumor microenvironment and may promote angiogenesis.

References

  1. Otani, T.; Furuse, M. Tight Junction Structure and Function Revisited. Trends Cell Biol. 2020, 30, 805–817.
  2. Hashimoto, Y.; Fukasawa, M.; Kuniyasu, H.; Yagi, K.; Kondoh, M. Claudin-targeted drug development using anti-claudin monoclonal antibodies to treat hepatitis and cancer. Ann. N. Y. Acad. Sci. 2017, 1397, 5–16.
  3. Osanai, M.; Takasawa, A.; Murata, M.; Sawada, N. Claudins in cancer: Bench to bedside. Pflug. Arch. Eur. J. Physiol. 2017, 469, 55–67.
  4. Morin, P.J. Claudin proteins in human cancer: Promising new targets for diagnosis and therapy. Cancer Res. 2005, 65, 9603–9606.
  5. Neesse, A.; Griesmann, H.; Gress, T.M.; Michl, P. Claudin-4 as therapeutic target in cancer. Arch. Biochem. Biophys. 2012, 524, 64–70.
  6. Zhu, J.L.; Gao, P.; Wang, Z.N.; Song, Y.X.; Li, A.L.; Xu, Y.Y.; Wang, M.X.; Xu, H.M. Clinicopathological significance of claudin-4 in gastric carcinoma. World J. Surg. Oncol. 2013, 11, 150.
  7. Resnick, M.B.; Gavilanez, M.; Newton, E.; Konkin, T.; Bhattacharya, B.; Britt, D.E.; Sabo, E.; Moss, S.F. Claudin expression in gastric adenocarcinomas: A tissue microarray study with prognostic correlation. Hum. Pathol. 2005, 36, 886–892.
  8. Nishiguchi, Y.; Fujiwara-Tani, R.; Sasaki, T.; Luo, Y.; Ohmori, H.; Kishi, S.; Mori, S.; Goto, K.; Yasui, W.; Sho, M.; et al. Targeting claudin-4 enhances CDDP-chemosensitivity in gastric cancer. Oncotarget 2019, 10, 2189–2202.
  9. Nichols, L.S.; Ashfaq, R.; Iacobuzio-Donahue, C.A. Claudin 4 protein expression in primary and metastatic pancreatic cancer: Support for use as a therapeutic target. Am. J. Clin. Pathol. 2004, 121, 226–230.
  10. Michl, P.; Buchholz, M.; Rolke, M.; Kunsch, S.; Lohr, M.; McClane, B.; Tsukita, S.; Leder, G.; Adler, G.; Gress, T.M. Claudin-4: A new target for pancreatic cancer treatment using Clostridium perfringens enterotoxin. Gastroenterology 2001, 121, 678–684.
  11. Sasaki, T.; Fujiwara-Tani, R.; Kishi, S.; Mori, S.; Luo, Y.; Ohmori, H.; Kawahara, I.; Goto, K.; Nishiguchi, Y.; Mori, T.; et al. Targeting claudin-4 enhances chemosensitivity of pancreatic ductal carcinomas. Cancer Med. 2019, 8, 6700–6708.
  12. De Oliveira, S.S.; de Oliveira, I.M.; De Souza, W.; Morgado-Díaz, J.A. Claudins upregulation in human colorectal cancer. FEBS Lett. 2005, 579, 6179–6185.
  13. Fujiwara-Tani, R.; Sasaki, T.; Luo, Y.; Goto, K.; Kawahara, I.; Nishiguchi, Y.; Kishi, S.; Mori, S.; Ohmori, H.; Kondoh, M.; et al. Anti-claudin-4 extracellular domain antibody enhances the antitumoral effects of chemotherapeutic and antibody drugs in colorectal cancer. Oncotarget 2018, 9, 37367–37378.
  14. Kolokytha, P.; Yiannou, P.; Keramopoulos, D.; Kolokythas, A.; Nonni, A.; Patsouris, E.; Pavlakis, K. Claudin-3 and claudin-4: Distinct prognostic significance in triple-negative and luminal breast cancer. Appl. Immunohistochem. Mol. Morphol. AIMM 2014, 22, 125–131.
  15. Ma, X.; Miao, H.; Jing, B.; Pan, Q.; Zhang, H.; Chen, Y.; Zhang, D.; Liang, Z.; Wen, Z.; Li, M. Claudin-4 controls the proliferation, apoptosis, migration and in vivo growth of MCF-7 breast cancer cells. Oncol. Rep. 2015, 34, 681–690.
  16. Luo, Y.; Kishi, S.; Sasaki, T.; Ohmori, H.; Fujiwara-Tani, R.; Mori, S.; Goto, K.; Nishiguchi, Y.; Mori, T.; Kawahara, I.; et al. Targeting claudin-4 enhances chemosensitivity in breast cancer. Cancer Sci. 2020, 111, 1840–1850.
  17. Naimi, A.; Zare, N.; Amjadi, E.; Soltan, M. High claudin-4 antigen expression in triple-negative breast cancer by the immunohistochemistry method. J. Res. Med. Sci. 2022, 27, 20.
  18. Nakashima, C.; Yamamoto, K.; Kishi, S.; Sasaki, T.; Ohmori, H.; Fujiwara-Tani, R.; Mori, S.; Kawahara, I.; Nishiguchi, Y.; Mori, T.; et al. Clostridium perfringens enterotoxin induces claudin-4 to activate YAP in oral squamous cell carcinomas. Oncotarget 2020, 11, 309–321.
  19. Rangel, L.B.; Agarwal, R.; D’Souza, T.; Pizer, E.S.; Alò, P.L.; Lancaster, W.D.; Gregoire, L.; Schwartz, D.R.; Cho, K.R.; Morin, P.J. Tight junction proteins claudin-3 and claudin-4 are frequently overexpressed in ovarian cancer but not in ovarian cystadenomas. Clin. Cancer Res. 2003, 9, 2567–2575.
  20. Kuwada, M.; Chihara, Y.; Luo, Y.; Li, X.; Nishiguchi, Y.; Fujiwara, R.; Sasaki, T.; Fujii, K.; Ohmori, H.; Fujimoto, K.; et al. Pro-chemotherapeutic effects of antibody against extracellular domain of claudin-4 in bladder cancer. Cancer Lett. 2015, 369, 212–221.
  21. Maesaka, F.; Kuwada, M.; Horii, S.; Kishi, S.; Fujiwara-Tani, R.; Mori, S.; Fujii, K.; Mori, T.; Ohmori, H.; Owari, T.; et al. Hypomethylation of CLDN4 Gene Promoter Is Associated with Malignant Phenotype in Urinary Bladder Cancer. Int. J. Mol. Sci. 2022, 23, 6516.
  22. Piontek, A.; Eichner, M.; Zwanziger, D.; Beier, L.S.; Protze, J.; Walther, W.; Theurer, S.; Schmid, K.W.; Führer-Sakel, D.; Piontek, J.; et al. Targeting claudin-overexpressing thyroid and lung cancer by modified Clostridium perfringens enterotoxin. Mol. Oncol. 2020, 14, 261–276.
  23. Bunthot, S.; Obchoei, S.; Kraiklang, R.; Pirojkul, C.; Wongkham, S.; Wongkham, C. Overexpression of claudin-4 in cholangiocarcinoma tissues and its possible role in tumor metastasis. Asian Pac. J. Cancer Prev. 2012, 13, 71–76.
  24. Tzelepi, V.N.; Tsamandas, A.C.; Vlotinou, H.D.; Vagianos, C.E.; Scopa, C.D. Tight junctions in thyroid carcinogenesis: Diverse expression of claudin-1, claudin-4, claudin-7 and occludin in thyroid neoplasms. Mod. Pathol. 2008, 21, 22–30.
  25. Coutinho-Camillo, C.M.; Lourenço, S.V.; da Fonseca, F.P.; Soares, F.A. Claudin expression is dysregulated in prostate adenocarcinomas but does not correlate with main clinicopathological parameters. Pathology 2011, 43, 143–148.
  26. Sheehan, G.M.; Kallakury, B.V.; Sheehan, C.E.; Fisher, H.A.; Kaufman, R.P., Jr.; Ross, J.S. Loss of claudins-1 and -7 and expression of claudins-3 and -4 correlate with prognostic variables in prostatic adenocarcinomas. Hum. Pathol. 2007, 38, 564–569.
  27. Nebbioso, A.; Tambaro, F.P.; Dell’Aversana, C.; Altucci, L. Cancer epigenetics: Moving forward. PLoS Genet. 2018, 14, e1007362.
  28. Feinberg, A.P. The Key Role of Epigenetics in Human Disease Prevention and Mitigation. N. Engl. J. Med. 2018, 378, 1323–1334.
  29. Kanwal, R.; Gupta, K.; Gupta, S. Cancer epigenetics: An introduction. Methods Mol. Biol. 2015, 1238, 3–25.
  30. Kwon, M.J.; Kim, S.S.; Choi, Y.L.; Jung, H.S.; Balch, C.; Kim, S.H.; Song, Y.S.; Marquez, V.E.; Nephew, K.P.; Shin, Y.K. Derepression of CLDN3 and CLDN4 during ovarian tumorigenesis is associated with loss of repressive histone modifications. Carcinogenesis 2010, 31, 974–983.
  31. Boireau, S.; Buchert, M.; Samuel, M.S.; Pannequin, J.; Ryan, J.L.; Choquet, A.; Chapuis, H.; Rebillard, X.; Avances, C.; Ernst, M.; et al. DNA-methylation-dependent alterations of claudin-4 expression in human bladder carcinoma. Carcinogenesis 2007, 28, 246–258.
  32. Hahn-Stromberg, V.; Askari, S.; Ahmad, A.; Befekadu, R.; Nilsson, T.K. Expression of claudin 1, claudin 4, and claudin 7 in colorectal cancer and its relation with CLDN DNA methylation patterns. Tumor Biol. 2017, 39, 1010428317697569.
  33. Kwon, M.J.; Kim, S.H.; Jeong, H.M.; Jung, H.S.; Kim, S.S.; Lee, J.E.; Gye, M.C.; Erkin, O.C.; Koh, S.S.; Choi, Y.L.; et al. Claudin-4 overexpression is associated with epigenetic derepression in gastric carcinoma. Lab. Investig. 2011, 91, 1652–1667.
  34. Ma, M.C.; Qian, H.; Ghassemi, F.; Zhao, P.; Xia, Y. Oxygen-sensitive δ-opioid receptor-regulated survival and death signals: Novel insights into neuronal preconditioning and protection. J. Biol. Chem. 2005, 280, 16208–16218.
  35. Litkouhi, B.; Kwong, J.; Lo, C.M.; Smedley, J.G., 3rd; McClane, B.A.; Aponte, M.; Gao, Z.; Sarno, J.L.; Hinners, J.; Welch, W.R.; et al. Claudin-4 overexpression in epithelial ovarian cancer is associated with hypomethylation and is a potential target for modulation of tight junction barrier function using a C-terminal fragment of Clostridium perfringens enterotoxin. Neoplasia 2007, 9, 304–314.
  36. Hasegawa, K.; Wakino, S.; Simic, P.; Sakamaki, Y.; Minakuchi, H.; Fujimura, K.; Hosoya, K.; Komatsu, M.; Kaneko, Y.; Kanda, T.; et al. Renal tubular Sirt1 attenuates diabetic albuminuria by epigenetically suppressing Claudin-1 overexpression in podocytes. Nat. Med. 2013, 19, 1496–1504.
  37. Di Cello, F.; Cope, L.; Li, H.; Jeschke, J.; Wang, W.; Baylin, S.B.; Zahnow, C.A. Methylation of the claudin 1 promoter is associated with loss of expression in estrogen receptor positive breast cancer. PLoS ONE 2013, 8, e68630.
  38. Hichino, A.; Okamoto, M.; Taga, S.; Akizuki, R.; Endo, S.; Matsunaga, T.; Ikari, A. Down-regulation of Claudin-2 Expression and Proliferation by Epigenetic Inhibitors in Human Lung Adenocarcinoma A549 Cells. J. Biol. Chem. 2017, 292, 2411–2421.
  39. Zhang, Z.; Yu, W.; Chen, S.; Chen, Y.; Chen, L.; Zhang, S. Methylation of the claudin3 promoter predicts the prognosis of advanced gastric adenocarcinoma. Oncol. Rep. 2018, 40, 49–60.
  40. Honda, H.; Pazin, M.J.; D’Souza, T.; Ji, H.; Morin, P.J. Regulation of the CLDN3 gene in ovarian cancer cells. Cancer Biol. Ther. 2007, 6, 1733–1742.
  41. Nishikiori, N.; Sawada, N.; Ohguro, H. Prevention of murine experimental corneal trauma by epigenetic events regulating claudin 6 and claudin 9. Jpn. J. Ophthalmol. 2008, 52, 195–203.
  42. Kudinov, A.E.; Deneka, A.; Nikonova, A.S.; Beck, T.N.; Ahn, Y.H.; Liu, X.; Martinez, C.F.; Schultz, F.A.; Reynolds, S.; Yang, D.H.; et al. Musashi-2 (MSI2) supports TGF-β signaling and inhibits claudins to promote non-small cell lung cancer (NSCLC) metastasis. Proc. Natl. Acad. Sci. USA 2016, 113, 6955–6960.
  43. Li, J.; Zhou, C.; Ni, S.; Wang, S.; Ni, C.; Yang, P.; Ye, M. Methylated claudin-11 associated with metastasis and poor survival of colorectal cancer. Oncotarget 2017, 8, 96249–96262.
  44. Jie, Y.; Ye, L.; Chen, H.; Yu, X.; Cai, L.; He, W.; Fu, Y. ELFN1-AS1 accelerates cell proliferation, invasion and migration via regulating miR-497-3p/CLDN4 axis in ovarian cancer. Bioengineered 2020, 11, 872–882.
  45. Satake, S.; Semba, S.; Matsuda, Y.; Usami, Y.; Chiba, H.; Sawada, N.; Kasuga, M.; Yokozaki, H. Cdx2 transcription factor regulates claudin-3 and claudin-4 expression during intestinal differentiation of gastric carcinoma. Pathol. Int. 2008, 58, 156–163.
  46. Kodera, Y.; Kohno, T.; Konno, T.; Arai, W.; Tsujiwaki, M.; Shindo, Y.; Chiba, H.; Miyakawa, M.; Tanaka, H.; Sakuma, Y.; et al. HMGB1 enhances epithelial permeability via p63/TGF-β signaling in lung and terminal bronchial epithelial cells. Tissue Barriers 2020, 8, 1805997.
  47. Nur Husna, S.M.; Md Shukri, N.; Tuan Sharif, S.E.; Tan, H.T.T.; Mohd Ashari, N.S.; Wong, K.K. IL-4/IL-13 Axis in Allergic Rhinitis: Elevated Serum Cytokines Levels and Inverse Association with Tight Junction Molecules Expression. Front. Mol. Biosci. 2022, 9, 819772.
  48. Yang, Y.; Cheon, S.; Jung, M.K.; Song, S.B.; Kim, D.; Kim, H.J.; Park, H.; Bang, S.I.; Cho, D. Interleukin-18 enhances breast cancer cell migration via down-regulation of claudin-12 and induction of the p38 MAPK pathway. Biochem. Biophys. Res. Commun. 2015, 459, 379–386.
  49. Rachakonda, G.; Vu, T.; Jin, L.; Samanta, D.; Datta, P.K. Role of TGF-β-induced Claudin-4 expression through c-Jun signaling in non-small cell lung cancer. Cell. Signal. 2016, 28, 1537–1544.
  50. Marincola Smith, P.; Choksi, Y.A.; Markham, N.O.; Hanna, D.N.; Zi, J.; Weaver, C.J.; Hamaamen, J.A.; Lewis, K.B.; Yang, J.; Liu, Q.; et al. Colon epithelial cell TGFβ signaling modulates the expression of tight junction proteins and barrier function in mice. Am. J. Physiol. Gastrointest. Liver Physiol. 2021, 320, G936–G957.
  51. Yan, T.; Tan, Y.; Deng, G.; Sun, Z.; Liu, B.; Wang, Y.; Yuan, F.; Sun, Q.; Hu, P.; Gao, L.; et al. TGF-β induces GBM mesenchymal transition through upregulation of CLDN4 and nuclear translocation to activate TNF-α/NF-κB signal pathway. Cell Death Dis. 2022, 13, 339.
  52. Kojima, T.; Kyuno, D.; Sawada, N. Targeting claudin-4 in human pancreatic cancer. Expert Opin. Ther. Targets 2012, 16, 881–887.
  53. Väre, P.; Soini, Y. Twist is inversely associated with claudins in germ cell tumors of the testis. APMIS 2010, 118, 640–647.
  54. Kim, B.; Breton, S. The MAPK/ERK-Signaling Pathway Regulates the Expression and Distribution of Tight Junction Proteins in the Mouse Proximal Epididymis. Biol. Reprod. 2016, 94, 22.
  55. Ishii, Y.; Saeki, K.; Liu, M.; Sasaki, F.; Koga, T.; Kitajima, K.; Meno, C.; Okuno, T.; Yokomizo, T. Leukotriene B4 receptor type 2 (BLT2) enhances skin barrier function by regulating tight junction proteins. FASEB J. 2016, 30, 933–947.
  56. Liu, H.; Zhang, Z.; Zhou, S.; Liu, X.; Li, G.; Song, B.; Xu, W. Claudin-1/4 as directly target gene of HIF-1α can feedback regulating HIF-1α by PI3K-AKT-mTOR and impact the proliferation of esophageal squamous cell though Rho GTPase and p-JNK pathway. Cancer Gene Ther. 2022, 29, 665–682.
  57. Batsaikhan, B.E.; Yoshikawa, K.; Kurita, N.; Iwata, T.; Takasu, C.; Kashihara, H.; Shimada, M. Cyclopamine decreased the expression of Sonic Hedgehog and its downstream genes in colon cancer stem cells. Anticancer Res. 2014, 34, 6339–6344.
  58. Yamada, G.; Murata, M.; Takasawa, A.; Nojima, M.; Mori, Y.; Sawada, N.; Takahashi, H. Increased expressions of claudin 4 and 7 in atypical adenomatous hyperplasia and adenocarcinoma of the lung. Med. Mol. Morphol. 2016, 49, 163–169.
  59. Seckin, Y.; Arici, S.; Harputluoglu, M.; Yonem, O.; Yilmaz, A.; Ozer, H.; Karincaoglu, M.; Demirel, U. Expression of claudin-4 and beta-catenin in gastric premalignant lesions. Acta Gastroenterol. Belg. 2009, 72, 407–412.
  60. Fujiwara-Tani, R.; Fujii, K.; Mori, S.; Kishi, S.; Sasaki, T.; Ohmori, H.; Nakashima, C.; Kawahara, I.; Nishiguchi, Y.; Mori, T.; et al. Role of Clostridium perfringens Enterotoxin on YAP Activation in Colonic Sessile Serrated Adenoma/Polyps with Dysplasia. Int. J. Mol. Sci. 2020, 21, 3840.
  61. Pan, X.Y.; Wang, B.; Che, Y.C.; Weng, Z.P.; Dai, H.Y.; Peng, W. Expression of claudin-3 and claudin-4 in normal, hyperplastic, and malignant endometrial tissue. Int. J. Gynecol. Cancer 2007, 17, 233–241.
  62. Sobel, G.; Páska, C.; Szabó, I.; Kiss, A.; Kádár, A.; Schaff, Z. Increased expression of claudins in cervical squamous intraepithelial neoplasia and invasive carcinoma. Hum. Pathol. 2005, 36, 162–169.
  63. Zhu, Y.; Brännström, M.; Janson, P.O.; Sundfeldt, K. Differences in expression patterns of the tight junction proteins, claudin 1, 3, 4 and 5, in human ovarian surface epithelium as compared to epithelia in inclusion cysts and epithelial ovarian tumours. Int. J. Cancer 2006, 118, 1884–1891.
  64. Turksen, K.; Troy, T.C. Junctions gone bad: Claudins and loss of the barrier in cancer. Biochim. Biophys. Acta 2011, 1816, 73–79.
  65. Escudero-Esparza, A.; Jiang, W.G.; Martin, T.A. The Claudin family and its role in cancer and metastasis. Front. Biosci. 2011, 16, 1069–1083.
  66. Pade, V.; Stavchansky, S. Estimation of the relative contribution of the transcellular and paracellular pathway to the transport of passively absorbed drugs in the Caco-2 cell culture model. Pharm. Res. 1997, 14, 1210–1215.
  67. Hicks, D.A.; Galimanis, C.E.; Webb, P.G.; Spillman, M.A.; Behbakht, K.; Neville, M.C.; Baumgartner, H.K. Claudin-4 activity in ovarian tumor cell apoptosis resistance and migration. BMC Cancer 2016, 16, 788.
  68. Pao, H.P.; Liao, W.I.; Tang, S.E.; Wu, S.Y.; Huang, K.L.; Chu, S.J. Suppression of Endoplasmic Reticulum Stress by 4-PBA Protects Against Hyperoxia-Induced Acute Lung Injury via Up-Regulating Claudin-4 Expression. Front. Immunol. 2021, 12, 674316.
  69. Singh, A.B.; Sharma, A.; Dhawan, P. Claudin-1 expression confers resistance to anoikis in colon cancer cells in a Src-dependent manner. Carcinogenesis 2012, 33, 2538–2547.
  70. Huang, J.; Zhang, L.; He, C.; Qu, Y.; Li, J.; Zhang, J.; Du, T.; Chen, X.; Yu, Y.; Liu, B.; et al. Claudin-1 enhances tumor proliferation and metastasis by regulating cell anoikis in gastric cancer. Oncotarget 2015, 6, 1652–1665.
  71. Osanai, M.; Murata, M.; Chiba, H.; Kojima, T.; Sawada, N. Epigenetic silencing of claudin-6 promotes anchorage-independent growth of breast carcinoma cells. Cancer Sci. 2007, 98, 1557–1562.
  72. Najafi, M.; Mortezaee, K.; Majidpoor, J. Cancer stem cell (CSC) resistance drivers. Life Sci. 2019, 234, 116781.
  73. Ayob, A.Z.; Ramasamy, T.S. Cancer stem cells as key drivers of tumour progression. J. Biomed. Sci. 2018, 25, 20.
  74. Kwon, M.J. Emerging roles of claudins in human cancer. Int. J. Mol. Sci. 2013, 14, 18148–18180.
  75. Kyuno, D.; Yamaguchi, H.; Ito, T.; Kono, T.; Kimura, Y.; Imamura, M.; Konno, T.; Hirata, K.; Sawada, N.; Kojima, T. Targeting tight junctions during epithelial to mesenchymal transition in human pancreatic cancer. World J. Gastroenterol. 2014, 20, 10813–10824.
  76. Papageorgis, P.; Lambert, A.W.; Ozturk, S.; Gao, F.; Pan, H.; Manne, U.; Alekseyev, Y.O.; Thiagalingam, A.; Abdolmaleky, H.M.; Lenburg, M.; et al. Smad signaling is required to maintain epigenetic silencing during breast cancer progression. Cancer Res. 2010, 70, 968–978.
  77. Sato, M.; Matsumoto, M.; Saiki, Y.; Alam, M.; Nishizawa, H.; Rokugo, M.; Brydun, A.; Yamada, S.; Kaneko, M.K.; Funayama, R.; et al. BACH1 Promotes Pancreatic Cancer Metastasis by Repressing Epithelial Genes and Enhancing Epithelial-Mesenchymal Transition. Cancer Res. 2020, 80, 1279–1292.
  78. Shrestha, A.; Uzal, F.A.; McClane, B.A. The interaction of Clostridium perfringens enterotoxin with receptor claudins. Anaerobe 2016, 41, 18–26.
  79. Gardelli, C.; Russo, L.; Cipolla, L.; Moro, M.; Andriani, F.; Rondinone, O.; Nicotra, F.; Sozzi, G.; Bertolini, G.; Roz, L. Differential glycosylation of collagen modulates lung cancer stem cell subsets through β1 integrin-mediated interactions. Cancer Sci. 2021, 112, 217–230.
  80. Moon, J.H.; Rho, Y.S.; Lee, S.H.; Koo, B.S.; Lee, H.J.; Do, S.I.; Cho, J.H.; Eun, Y.G.; Park, M.W.; Shin, H.A.; et al. Role of integrin β1 as a biomarker of stemness in head and neck squamous cell carcinoma. Oral Oncol. 2019, 96, 34–41.
  81. Lu, Z.; Kim, D.H.; Fan, J.; Lu, Q.; Verbanac, K.; Ding, L.; Renegar, R.; Chen, Y.H. A non-tight junction function of claudin-7-Interaction with integrin signaling in suppressing lung cancer cell proliferation and detachment. Mol. Cancer 2015, 14, 120.
  82. Kim, D.H.; Lu, Q.; Chen, Y.H. Claudin-7 modulates cell-matrix adhesion that controls cell migration, invasion and attachment of human HCC827 lung cancer cells. Oncol. Lett. 2019, 17, 2890–2896.
  83. Owari, T.; Sasaki, T.; Fujii, K.; Fujiwara-Tani, R.; Kishi, S.; Mori, S.; Mori, T.; Goto, K.; Kawahara, I.; Nakai, Y.; et al. Role of Nuclear Claudin-4 in Renal Cell Carcinoma. Int. J. Mol. Sci. 2020, 21, 8340.
  84. Yu, S.; Zhang, Y.; Li, Q.; Zhang, Z.; Zhao, G.; Xu, J. CLDN6 promotes tumor progression through the YAP1-snail1 axis in gastric cancer. Cell Death Dis. 2019, 10, 949.
  85. Kong, F.E.; Li, G.M.; Tang, Y.Q.; Xi, S.Y.; Loong, J.H.C.; Li, M.M.; Li, H.L.; Cheng, W.; Zhu, W.J.; Mo, J.Q.; et al. Targeting tumor lineage plasticity in hepatocellular carcinoma using an anti-CLDN6 antibody-drug conjugate. Sci. Transl. Med. 2021, 13, eabb6282.
  86. Zhou, B.; Flodby, P.; Luo, J.; Castillo, D.R.; Liu, Y.; Yu, F.X.; McConnell, A.; Varghese, B.; Li, G.; Chimge, N.O.; et al. Claudin-18-mediated YAP activity regulates lung stem and progenitor cell homeostasis and tumorigenesis. J. Clin. Investig. 2018, 128, 970–984.
  87. Kohmoto, T.; Masuda, K.; Shoda, K.; Takahashi, R.; Ujiro, S.; Tange, S.; Ichikawa, D.; Otsuji, E.; Imoto, I. Claudin-6 is a single prognostic marker and functions as a tumor-promoting gene in a subgroup of intestinal type gastric cancer. Gastric Cancer 2020, 23, 403–417.
  88. Hao, S.; Yang, C.; Song, P.; Shi, H.; Zou, Y.; Chen, M.; Wu, X.; Yin, Y.; Yu, Z.; Zhu, W.; et al. CLDN4 promotes growth of acute myeloid leukemia cells via regulating AKT and ERK1/2 signaling. Biochem. Biophys. Res. Commun. 2022, 619, 137–143.
  89. Wang, P.; Liu, T.; Zhao, Z.; Wang, Z.; Liu, S.; Yang, X. SPTBN2 regulated by miR-424-5p promotes endometrial cancer progression via CLDN4/PI3K/AKT axis. Cell Death Discov. 2021, 7, 382.
  90. Luo, J.; Wang, H.; Chen, H.; Gan, G.; Zheng, Y. CLDN4 silencing promotes proliferation and reduces chemotherapy sensitivity of gastric cancer cells through activation of the PI3K/Akt signalling pathway. Exp. Physiol. 2020, 105, 979–988.
  91. Shang, X.; Lin, X.; Howell, S.B. Claudin-4 controls the receptor tyrosine kinase EphA2 pro-oncogenic switch through β-catenin. Cell Commun. Signal. 2014, 12, 59.
  92. Hashimoto, Y.; Okada, Y.; Shirakura, K.; Tachibana, K.; Sawada, M.; Yagi, K.; Doi, T.; Kondoh, M. Anti-Claudin Antibodies as a Concept for Development of Claudin-Directed Drugs. J. Pharmacol. Exp. Ther. 2019, 368, 179–186.
  93. Kato-Nakano, M.; Suzuki, M.; Kawamoto, S.; Furuya, A.; Ohta, S.; Nakamura, K.; Ando, H. Characterization and evaluation of the antitumour activity of a dual-targeting monoclonal antibody against claudin-3 and claudin-4. Anticancer Res. 2010, 30, 4555–4562.
  94. Li, X.; Iida, M.; Tada, M.; Watari, A.; Kawahigashi, Y.; Kimura, Y.; Yamashita, T.; Ishii-Watabe, A.; Uno, T.; Fukasawa, M.; et al. Development of an anti-claudin-3 and -4 bispecific monoclonal antibody for cancer diagnosis and therapy. J. Pharmacol. Exp. Ther. 2014, 351, 206–213.
  95. Suzuki, M.; Kato-Nakano, M.; Kawamoto, S.; Furuya, A.; Abe, Y.; Misaka, H.; Kimoto, N.; Nakamura, K.; Ohta, S.; Ando, H. Therapeutic antitumor efficacy of monoclonal antibody against Claudin-4 for pancreatic and ovarian cancers. Cancer Sci. 2009, 100, 1623–1630.
  96. Mitchell, L.A.; Koval, M. Specificity of interaction between clostridium perfringens enterotoxin and claudin-family tight junction proteins. Toxins 2010, 2, 1595–1611.
  97. Romanov, V.; Whyard, T.C.; Waltzer, W.C.; Gabig, T.G. A claudin 3 and claudin 4-targeted Clostridium perfringens protoxin is selectively cytotoxic to PSA-producing prostate cancer cells. Cancer Lett. 2014, 351, 260–264.
  98. Landers, K.A.; Samaratunga, H.; Teng, L.; Buck, M.; Burger, M.J.; Scells, B.; Lavin, M.F.; Gardiner, R.A. Identification of claudin-4 as a marker highly overexpressed in both primary and metastatic prostate cancer. Br. J. Cancer 2008, 99, 491–501.
  99. Liang, Z.Y.; Kang, X.; Chen, H.; Wang, M.; Guan, W.X. Effect of Clostridium perfringens enterotoxin on gastric cancer cells SGC7901 which highly expressed claudin-4 protein. World J. Gastrointestig. Oncol. 2017, 9, 153–159.
  100. Tanaka, S.; Aoyama, T.; Ogawa, M.; Takasawa, A.; Murata, M.; Osanai, M.; Saito, T.; Sawada, N. Cytotoxicity of Clostridium perfringens enterotoxin depends on the conditions of claudin-4 in ovarian carcinoma cells. Exp. Cell Res. 2018, 371, 278–286.
  101. English, D.P.; Santin, A.D. Claudins overexpression in ovarian cancer: Potential targets for Clostridium Perfringens Enterotoxin (CPE) based diagnosis and therapy. Int. J. Mol. Sci. 2013, 14, 10412–10437.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license; additional terms may apply. By using this site, you agree to the Terms and Conditions and Privacy Policy.
Upload a video for this entry
Information
Subjects: Oncology
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Rina Fujiwara-Tani
,
Shiori Mori
,
Ruiko Ogata
,
Rika Sasaki
,
Ayaka Ikemoto
,
Shingo Kishi
,
Masuo Kondoh
,
Hiroki Kuniyasu
View Times: 489
Revisions: 2 times (View History)
Update Date: 25 May 2023
Table of Contents
    1000/1000
    Hot Most Recent
    Video Production Service
    Feedback