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Cystatin C Antagonizes Transforming Growth Factor β Signaling in Normal and Cancer Cells
Abstract
Cystatin C (CystC) is a secreted cysteine protease inhibitor that regulates bone resorption, neutrophil chemotaxis, and tissue inflammation, as well as resistance to bacterial and viral infections. CystC is ubiquitously expressed and present in most bodily fluids where it inhibits the activities of cathepsins, a family of cysteine proteases that can promote cancer cell invasion and metastasis. Transforming growth factor β (TGF-β) is a multifunctional cytokine endowed with both tumor-suppressing and tumor-promoting activities. We show herein that TGF-β treatment up-regulated CystC transcript and protein in murine 3T3-L1 fibroblasts. Moreover, CystC mRNA expression was down-regulated in ∼50% of human malignancies, particularly cancers of the stomach, uterus, colon, and kidney. Overexpression of CystC in human HT1080 fibrosarcoma cells antagonized their invasion through synthetic basement membranes in part via a cathepsin-dependent pathway. Independent of effects on cathepsin activity, CystC also reduced HT1080 cell gene expression stimulated by TGF-β. Invasion of 3T3-L1 cells occurred through both cathepsin- and TGF-β-dependent pathways. Both pathways were blocked by CystC, but only the TGF-β-dependent pathway was blocked by a CystC mutant (i.e., Δ14CystC) that is impaired in its ability to inhibit cathepsin activity. Moreover, CystC and Δ14CystC both inhibited 3T3-L1 cell gene expression stimulated by TGF-β. We further show that CystC antagonized TGF-β binding to its cell surface receptors, doing so by interacting physically with the TGF-β type II receptor and antagonizing its binding of TGF-β. Collectively, our findings have identified CystC as a novel TGF-β receptor antagonist, as well as a novel CystC-mediated feedback loop that inhibits TGF-β signaling.
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“Cystatin C has been reported to antagonize TGF-β signaling through interaction with TGF-βRII49.”
From Oligomeric cystatin C supports the immunosuppressive activity of myeloid cells through interaction with inhibitory receptors (2025) · cites this paper as [49]
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Cites
Role of Transforming Growth Factor β in Human Disease
Blobe, G. C., Schiemann, W. P., & Lodish, H. F. (2000) · New England Journal of Medicine · doi:10.1056/nejm200005043421807 · Cited by 2,453
Self-citationTGFβ Signaling in Growth Control, Cancer, and Heritable Disorders
Massagué, J., Blain, S. W., & Lo, R. S. (2000) · Cell · doi:10.1016/s0092-8674(00)00121-5 · Cited by 2,391
The microenvironment of the tumour–host interface
Liotta, L. A., & Kohn, E. C. (2001) · Nature · doi:10.1038/35077241 · Cited by 2,330
TGF-β Signaling in Tumor Suppression and Cancer Progression
Derynck, R., Akhurst, R. J., & Balmain, A. (2001) · Nature Genetics · doi:10.1038/ng1001-117 · Cited by 2,275
Massagué, J. (2000) · Nature Reviews Molecular Cell Biology · doi:10.1038/35043051 · Cited by 1,925
TGFβ signals through a heteromeric protein kinase receptor complex
Wrana, J. L., Attisano, L., Cárcamo, J. M., Zentella‐Dehesa, A., Doody, J. F., Laiho, M., Wang, X.-F., & Massagué, J. (1992) · Cell · doi:10.1016/0092-8674(92)90395-s · Cited by 1,528
Lysosomal cysteine proteases: more than scavengers
Turk, B., Turk, D., & Türk, V. (2000) · Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology · doi:10.1016/s0167-4838(99)00263-0 · Cited by 844
Cystatin C: An Improved Estimator of Glomerular Filtration Rate?
Laterza, O., Price, C. P., & Scott, M. G. (2002) · Clinical Chemistry · doi:10.1093/clinchem/48.5.699 · Cited by 658
Bode, W., Engh, R. A., Müsil, D., Thiele, U., Huber, R., Karshikov, A., Brzin, J., Kos, J., & Türk, V. (1988) · The EMBO Journal · doi:10.1002/j.1460-2075.1988.tb03109.x · Cited by 594
Heterotypic Signaling between Epithelial Tumor Cells and Fibroblasts in Carcinoma Formation
Elenbaas, B., & Weinberg, R. A. (2001) · Experimental Cell Research · doi:10.1006/excr.2000.5133 · Cited by 572
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Research works printed but not linked: 4
- Kos J, Krasovec M, Cimerman N, Nielsen HJ, Christensen IJ, Brunner N. Cysteine proteinase inhibitors stefin A, stefin B, and cystatin C in sera from patients with colorectal cancer: relation to prognosis. Clin Cancer Res, 2000;6:505–11.
- Szpaderska AM, Frankfater A. An intracellular form of cathepsin B contributes to invasiveness in cancer. Cancer Res, 2001;61:3493–500.
- Rowland-Goldsmith MA, Maruyama H, Kusama T, Ralli S, Korc M. Soluble type II transforming growth factor-β (TGF-β) receptor inhibits TGF-β signaling in COLO-357 pancreatic cancer cells in vitro and attenuates tumor formation. Clin Cancer Res, 2001;7:2931–40.
- Won J, Kim H, Park EJ, Hong Y, Kim SJ, Yun Y. Tumorigenicity of mouse thymoma is suppressed by soluble type II transforming growth factor β receptor therapy. Cancer Res, 1999;59:1273–7.
Cited by
Sorted by citations
Items 101–163 of 163
Differential Analysis of the Secretome of WRL68 Cells Infected with the Chikungunya Virus
Thio, C. L., Yusof, R., Ashrafzadeh, A., Bahari, S., Abdul‐Rahman, P. S., & Karsani, S. A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0129033 · Cited by 14
Cystatin C expression is increased in the hippocampus following photothrombotic stroke in rat
Pirttilä, T. J., & Pitkänen, A. (2005) · Neuroscience Letters · doi:10.1016/j.neulet.2005.10.091 · Cited by 14
Casey, T., Mulvey, T. M., Patnode, T. A., Dean, A., Zakrzewska, E. I., & Plaut, K. I. (2007) · Experimental Biology and Medicine · doi:10.3181/0609-rm-218 · Cited by 13
Expression of Cystatin C in human stomach neoplasms
Li, L. (2010) · Molecular Medicine Reports · doi:10.3892/mmr_00000304 · Cited by 13
Expression of Cystatin C in Human Esophageal Cancer
Zeng, Q., Zhao, Y., Yang, Y., Zheng, G., Wang, G., Zhang, P., Cui, Y., Su, S., & Li, K. (2011) · Tumori Journal · doi:10.1177/030089161109700212 · Cited by 13
Yuan, J., Xu, M., Li, J., Li, N., Chen, L.-Z., Feng, Q.-S., & Zeng, Y.-X. (2016) · Clinics · doi:10.6061/clinics/2016(06)09 · Cited by 13
Yang, L., Wei, Q., Tan, P., Shi, M., Chen, J., Xu, H., Xie, N., Xu, H., Jiang, Y. H., Ai, J., et al. (2019) · Asian Journal of Andrology · doi:10.4103/aja.aja_84_18 · Cited by 13
Rieswijk, L., Brauers, K. J. J., Coonen, M. L. J., Jennen, D. G. J., Breda, S. G. J. V., & Kleinjans, J. C. S. (2016) · Mutagenesis · doi:10.1093/mutage/gew027 · Cited by 11
Shen, Y., Zhang, X., Li, C., Wang, X., Ye, Y., Yuan, J., Gong, H., Zou, Y., & Ge, J. (2020) · Annals of Translational Medicine · doi:10.21037/atm-20-7041 · Cited by 11
Association of cystatin C with prostasomes in human seminal plasma
Carlsson, L., Ronquist, G. K., Ronquist, G. K., ELIASSON, R., Egberg, N., & Larsson, A. O. (2010) · International Journal of Andrology · doi:10.1111/j.1365-2605.2010.01090.x · Cited by 11
Suppressed dendritic cell functions by cystatin C lead to compromised immunity in vivo
Chen, S., Liu, L., Zhang, W., Sun, L. J., Wang, F., Zhao, Y., Liu, S., Zhao, L., & Xu, Y. (2020) · Cellular Immunology · doi:10.1016/j.cellimm.2020.104049 · Cited by 10
Expression of cystatin C and its effect on EC9706 cells in esophageal carcinoma.
Yan, Y., Zhou, K., Wang, L., Zhou, Y., Chen, X., & Fan, Q. (2015) · PubMed Central · Cited by 10
Cao, Z., Xiao, G., Zhang, W., Ji, J., Ye, C., Liu, D., Tian, Q., & Sun, Y. (2019) · Journal of Cancer · doi:10.7150/jca.31725 · Cited by 11
Cystatin C as a predictor factor in patients with renal cell carcinoma treated by everolimus
Bodnar, L., Stec, R., Dzierżanowska, M., Synowiec, A., Cierniak, S., Kade, G., & Szczylik, C. A. (2016) · Cancer Chemotherapy and Pharmacology · doi:10.1007/s00280-016-3084-9 · Cited by 10
Snorradóttir, Á. Ó., Ísaksson, H. J., Ingþórsson, S., Ólafsson, E., Pálsdóttir, Á., & Bragason, B. Þ. (2017) · Laboratory Investigation · doi:10.1038/labinvest.2016.133 · Cited by 10
Cystatin C as a potential biomarker to evaluate migraine
Akdağ, T., & Uca, A. U. (2020) · Arquivos de Neuro-Psiquiatria · doi:10.1590/0004-282x20200005 · Cited by 9
Orimoto, A., Kurokawa, M., Handa, K., Ishikawa, M., Nishida, E., Aino, M., Mitani, A., Ogawa, M., Tsuji, T., & Saito, M. (2017) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2017.02.019 · Cited by 9
Snorradottir, A. O., Hakonarson, H., & Palsdottir, A. (2024) · Brain Pathology · doi:10.1111/bpa.13291 · Cited by 7
Human cystatin C in fibrotic diseases
Lalmanach, G., Rigoux, B., David, A., Tahri-Joutey, M., Lecaille, F., Marchand-Adam, S., & Saidi, A. (2024) · Clinica Chimica Acta · doi:10.1016/j.cca.2024.120016 · Cited by 8
Majewska, E., Wittek, N., Rysz, J., & Baj, Z. (2012) · Medical Science Monitor · doi:10.12659/msm.883545 · Cited by 8
Lu, S., & Li, S. (2022) · Cancer Medicine · doi:10.1002/cam4.4731 · Cited by 7
Externally added cystatin C reduces growth of A375 melanoma cells by increasing cell cycle time
Wallin, H., Hunaiti, S., & Abrahamson, M. (2021) · FEBS Open Bio · doi:10.1002/2211-5463.13162 · Cited by 6
Frygelius, J., Arvestad, L., Wedell, A., & Töhönen, V. (2010) · Evolution & Development · doi:10.1111/j.1525-142x.2010.00418.x · Cited by 6
Current Thoughts on the Therapeutic Potential of Stem Cell
Rameshwar, P. (2012) · Methods in molecular biology · doi:10.1007/978-1-61779-815-3_1 · Cited by 6
Chemotherapeutic targeting of the TGF-β pathway in breast cancers
Lee, Y., & Schiemann, W. P. (2013) · Breast Cancer Management · doi:10.2217/bmt.13.74 · Cited by 6
Self-citationEgg white cystatin isolation and its medical application.
Trziszka, T., Polanowski, A., Saleh, Y., & Kopeć, W. (2006) · EPC 2006 - 12th European Poultry Conference, Verona, Italy, 10-14 September, 2006 · Cited by 4
An Update on the Therapeutic Potential of Stem Cells
Rameshwar, P., Moore, C. A., Shah, N. N., & Smith, C. P. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-8697-2_1 · Cited by 4
Role of Cystatins in Tumor Neovascularization
Keppler, D., & Sierra, F. (2005) · Future Oncology · doi:10.2217/14796694.1.5.661 · Cited by 4
Tholen, S., Koczorowska, M. M., Lai, Z. W., Dengjel, J., & Schilling, O. (2013) · Springer eBooks · doi:10.1007/978-3-7091-0885-7_5 · Cited by 3
Tian, X., Zhang, X., Yu, M., Lü, Y., Ding, Z., Huang, M., Peng, F., Ren, L., Wang, J., Wang, Y., et al. (2017) · International Journal of Clinical Oncology · doi:10.1007/s10147-017-1206-y · Cited by 3
Xie, Q., Wan, R., Xu, L., & Lin, J. (2008) · PubMed · Cited by 3
Zhang, C., He, Y., Liu, X., Xie, J., Fang, M., Yang, X., Huang, R., Lou, Q., Li, B., Gupta, A., et al. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02462-x · Cited by 2
Tan, X.-R., Huang, S., Gong, S., Chen, Y., Yang, X., He, Q., He, S., Liu, N., & Li, Y.-Q. (2021) · OncoTargets and Therapy · doi:10.2147/ott.s286009 · Cited by 2
Pálsdóttir, Á., Snorradóttir, Á. Ó., & Hakonarson, H. H. (2022) · Læknablaðið · doi:10.17992/lbl.2022.12.721 · Cited by 2
Niche Induces Dedifferentiation
Kapoor, P. S. A. (2013) · Journal of Bioanalysis & Biomedicine · doi:10.4172/1948-593x.1000089 · Cited by 2
Ratna, A., & Das, S. K. (2017) · Springer eBooks · doi:10.1007/978-981-10-6141-7_8 · Cited by 2
Lu, S., Wang, Y., Zhou, Z., Zhang, Y., Yang, L., & Yang, X. (2025) · Updates in Surgery · doi:10.1007/s13304-025-02208-y · Cited by 1
Snorradóttir, Á. Ó., Hafsteinsson, H. K., Hansdottir, K., Ingþórsson, S., Gudmundsson, S. R., Skodras, A., Ísaksson, H. J., & Hakonarson, H. H. (2026) · Acta Neuropathologica Communications · doi:10.1186/s40478-026-02233-x · Cited by 1
Cystatin C Decreases The Body Temperature And Pain Perception In Rats
Navarro, L., & Tit, P. (2012) · Cited by 1
The Homology Modeling and Docking Investigation of Human Cathepsin B
Khara, A., Jahangirian, E., & Tarrahimofrad, H. (2020) · International Journal of Medical Toxicology and Forensic Medicine · doi:10.32598/ijmtfm.v10i1.26687 · Cited by 1
McKelvey, M. C., Bradbury, I., McDowell, C., Calfee, C. S., Weldon, S., O’Kane, C. M., McAuley, D. F., & Taggart, C. C. (2022) · Critical Care and Resuscitation · doi:10.51893/2022.3.oa4 · Cited by 1
Veillard, F. (2009) · theses.fr (ABES) · doi:10.70675/4b336dc1z1a12z4417za2f3z202b8f929d2b · Cited by 1
Rodent malaria parasites : genome organization & comparative genomics
Kooij, T. W. A. (2006) · Leiden Repository (Leiden University)
The Testatin/Cres subgroup of family 2 cystatins in sexual development
Frygelius, J. (2009) · Figshare
Role of TGF-β in Osteolytic Bone Metastases
Bartholin, L., & Guise, T. A. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-293-9_7
Rakvaag, H. (2007) · NORA - Norwegian Open Research Archives
EXTRACTION OF CYSTATIN (ENZYME INHIBITORS) FROM ANIMAL SLAUGHTERHOUSE WASTES
Somasundaram, H. N. (2013) · Library and Archives Canada (Government of Canada)
Wallin, H. (2013) · Lund University Publications (Lund University)
The structure of carbon monoxide myoglobin: real-space refinement.
Norvell, J. C., & SCHOENBORN, B. P. (1976) · PubMed
Uptake of Cystatin by Melanoma Cells in Culture
Deady, L. E., & Cox, J. L. (2013) · CellBio · doi:10.4236/cellbio.2013.22008
Sebzda, T., Gburek, J., Pfanhauser, M., Pilecki, W., & Warwas, M. (2009)
King, C., Patel, S. A., Arinzeh, T. L., & Rameshwar, P. (2009) · Springer eBooks · doi:10.1007/978-90-481-3375-8_17
Cystatine C : point d'étape et perspectives Cystatin C: current step and future prospects
Delanaye, P., Piéroni, L., Mariat, C., & Froissart, M. (2008)
Dalgleish, R. W. M., Francis, T., Beckman, M. J., Murray, S. S., Brochmann, E. J., & Behnam, K. (2006) · Journal of Orthopaedic Research® · doi:10.1002/jor.20072
Role of Shear Stress in the Differential Regulation of Endothelial Cathepsins and Cystatin C
Platt, M. O. (2006) · UPT. Syiah Kuala University Library (Syiah Kuala University)
MicroRNAs and epigenetics in chemical carcinogenesis : an integrative toxicogenomics-based approach
Rieswijk, L. (2016) · Research Publications (Maastricht University) · doi:10.26481/dis.20160120lr
In memory of Michael Heyd (1943-2014)
Peset, J. L. (2016) · Culture & History Digital Journal · doi:10.3989/chdj.2016.021
Distribution of cathepsin L in human umbilical cord tissues
Gogiel, T., Wolańska, M., Galewska, Z., Kinalski, P., Sobolewski, K., & Romanowicz, L. (2017) · Acta Biochimica Polonica · doi:10.18388/abp.2017_1513
Antonio Muñoz Molina "No tengo nostalgia porque es lo contrario de la memoria"
Blanco, N. (2006) · Cambio 16
Akbulut, E. D., Erdoğan, S., Akbulut, S., & Yılmaz, F. M. (2020) · Harran Üniversitesi Tıp Fakültesi Dergisi · doi:10.35440/hutfd.689952
The role of peptidases and their endogenous inhibitors in the regulation of NK cell cytotoxicity
Kos, J., Jewett, A., Pišlar, A. H., Jakoš, T., Senjor, E., & Nanut, M. P. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-824375-6.00004-7
(2004) · Clinical Chemistry and Laboratory Medicine (CCLM) · doi:10.1515/cclm.2004.240
Metadata
- Authors
- Sokol, J. P., & Schiemann, W. P.
- Affiliations
- National Jewish Health (US)
- Venue
- Molecular Cancer Research
- Published
- 2004-03-01
- Volume
- 2
- Issue
- 3
- Pages
- 183-195
- ISSN
- 1541-7786 (ISSN-L)
- 1557-3125
- OpenAlex
- W4292964442
- Cited by
- 121
- References
- 60
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 2 · 2023: 4 · 2022: 3 · 2021: 5 · 2020: 5 · 2019: 1 · 2018: 10 · 2017: 10 · 2016: 8 · 2015: 3 · 2014: 4 · 2013: 5 · 2012: 2
- FWCI
- 3.08
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Molecular Cancer Research (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Protease and Inhibitor Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mechanisms of cancer metastasis
- Keywords
- cystatin C, TGF-beta, TGF-beta signaling, cathepsins, cysteine protease inhibitors, TGFBR2, cell invasion, fibroblasts, fibrosarcoma, cancer gene expression, tumor suppression
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