Abstract
The protease-activated receptor-2 (PAR-2) is a G protein-coupled receptor that is cleaved and activated by trypsin. We investigated the expression of PAR-2 and the role of trypsin in cell proliferation in human colon cancer cell lines. A total of 10 cell lines were tested for expression of PAR-2 mRNA by Northern blot and RT-PCR. PAR-2 protein was detected by immunofluorescence. Trypsin and the peptide agonist SLIGKV (AP2) were tested for their ability to induce calcium mobilization and to promote cell proliferation on serum-deprived cells. PAR-2 mRNA was detected by Northern blot analysis in 6 out of 10 cell lines [HT-29, Cl.19A, Caco-2, SW480, HCT-8 and T84]. Other cell lines expressed low levels of transcripts, which were detected only by RT-PCR. Further results were obtained with HT-29 cells: (1) PAR-2 protein is expressed at the cell surface; (2) an increase in intracellular calcium concentration was observed upon trypsin (1–100 nM) or AP2 (10–100 μM) challenges; (3) cells grown in serum-deprived media supplemented with trypsin (0.1–1 nM) or AP2 (1–300 μM) exhibited important mitogenic responses (3-fold increase of cell number). Proliferative effects of trypsin or AP2 were also observed in other cell lines expressing PAR-2. These data show that subnanomolar concentrations of trypsin, acting at PAR-2, promoted the proliferation of human colon cancer cells. The results of this study indicate that trypsin could be considered as a growth factor and unravel a new mechanism whereby serine proteases control colon tumours. © 2001 Cancer Research Campaign www.bjcancer.com
Similar content being viewed by others
Article PDF
Change history
16 November 2011
This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication
References
Akers, IA, Parsons, M, Hill, MR, Hollenberg, MD, Sanjar, S, Laurent, GJ & McAnulty, RJ (2000). Mast cell tryptase stimulates human lung fibroblast proliferation via protease-activated receptor-2. Am J Physiol Lung Cell Mol Physiol, 278, L193–201.
Aldenborg, F & Enerback, L (1994). The immunohistochemical demonstration of chymase and tryptase in human intestinal mast cells. Histochem J, 26, 587–596.
Augeron, C & Laboisse, CL (1984). Emergence of permanently differentiated cell clones in a human colonic cancer cell line in culture after treatment with sodium butyrate. Cancer Res, 44, 3961–3969.
Belham, CM, Tate, RJ, Scott, PH, Pemberton, AD, Miller, HR, Wadsworth, RM, Gould, GW & Plevin, R (1996). Trypsin stimulates proteinase-activated receptor-2-dependent and -independent activation of mitogen-activated protein kinases. Biochem J, 320, 939–946.
Bernard-Perrone, F, Carrere, J, Renaud, W, Moriscot, C, Thoreux, K, Bernard, P, Servin, A, Balas, D & Senegas-Balas, F (1998). Pancreatic trypsinogen I expression during cell growth and differentiation of two human colon carcinoma cells. Am J Physiol, 274, G1077–1086.
Blackhart, BD, Emilsson, K, Nguyen, D, Teng, W, Martelli, AJ, Nystedt, S, Sundelin, J & Scarborough, RM (1996). Ligand cross-reactivity within the protease-activated receptor family. J Biol Chem, 271, 16466–16471.
Blasi, F & Stoppelli, MP (1999). Proteases and cancer invasion: from belief to certainty. AACR meeting on proteases and protease inhibitors in cancer, Nyborg, Denmark, 14–18 June 1998. Biochim Biophys Acta, 1423, R35–R44.
Blumberg, PM & Robbins, PW (1975). Effect of proteases on activation of resting chick embryo fibroblasts and on cell surface proteins. Cell, 6, 137–147.
Bohm, SK, Khitin, LM, Grady, EF, Aponte, G, Payan, DG & Bunnett, NW (1996a). Mechanisms of desensitization and resensitization of proteinase-activated receptor-2. J Biol Chem, 271, 22003–22016.
Bohm, SK, Kong, W, Bromme, D, Smeekens, SP, Anderson, DC, Connolly, A, Kahn, M, Nelken, NA, Coughlin, SR, Payan, DG & Bunnett, NW (1996b). Molecular cloning, expression and potential functions of the human proteinase-activated receptor-2. Biochem J, 314, 1009–1016.
Bustos, D, Tiscornia, O, Caldarini, MI, Negri, G, Pons, S, Ogawa, K & De Paula, JA (1994). Colonic proteolysis following pancreatic duct ligation in the rat. Int J Pancreatol, 16, 45–49.
Carney, DH & Cunningham, DD (1977). Initiation of check cell division by trypsin action at the cell surface. Nature, 268, 602–606.
Chirgwin, JM, Przybyla, AE, MacDonald, RJ & Rutter, WJ (1979). Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry, 18, 5294–5299.
D’Andrea, MR, Derian, CK, Leturcq, D, Baker, SM, Brunmark, A, Ling, P, Darrow, AL, Santulli, RJ, Brass, LF & Andrade-Gordon, P (1998). Characterization of protease-activated receptor-2 immunoreactivity in normal human tissues. J Histochem Cytochem, 46, 157–164.
Darmoul, D, Lacasa, M, Baricault, L, Marguet, D, Sapin, C, Trotot, P, Barbat, A & Trugnan, G (1992). Dipeptidyl peptidase IV (CD 26) gene expression in enterocyte-like colon cancer cell lines HT-29 and Caco-2. Cloning of the complete human coding sequence and changes of dipeptidyl peptidase IV mRNA levels during cell differentiation. J Biol Chem, 267, 4824–4833.
DeFea, KA, Zalevsky, J, Thoma, MS, Dery, O, Mullins, RD & Bunnett, NW (2000). beta-arrestin-dependent endocytosis of proteinase-activated receptor 2 is required for intracellular targeting of activated ERK1/2. J Cell Biol, 148, 1267–1281.
Dery, O, Corvera, CU, Steinhoff, M & Bunnett, NW (1998). Proteinase-activated receptors: novel mechanisms of signaling by serine proteases. Am J Physiol, 274, C1429–1452.
Green, GM & Nasset, ES (1980). Importance of bile in regulation of intraluminal proteolytic enzyme activities in the rat. Gastroenterology, 79, 695–702.
Hedstrom, J, Haglund, C, Haapiainen, R & Stenman, UH (1996). Serum trypsinogen-2 and trypsin-2-alpha(1)-antitrypsin complex in malignant and benign digestive-tract diseases. Preferential elevation in patients with cholangiocarcinomas. Int J Cancer, 66, 326–331.
Hirahara, F, Miyagi, Y, Miyagi, E, Yasumitsu, H, Koshikawa, N, Nagashima, Y, Kitamura, H, Minaguchi, H, Umeda, M & Miyazaki, K (1995). Trypsinogen expression in human ovarian carcinomas. Int J Cancer, 63, 176–181.
Hollenberg, MD (1996). Protease-mediated signalling: new paradigms for cell regulation and drug development. Trends Pharmacol Sci, 17, 3–6.
Hollenberg, MD, Saifeddine, M, al-Ani, B & Kawabata, A (1997). Proteinase-activated receptors: structural requirements for activity, receptor cross-reactivity, and receptor selectivity of receptor-activating peptides. Can J Physiol Pharmacol, 75, 832–841.
Ichikawa, Y, Koshikawa, N, Hasegawa, S, Ishikawa, T, Momiyama, N, Kunizaki, C, Takahashi, M, Moriwaki, Y, Akiyama, H, Yamaoka, H, Yanoma, S, Tsuburaya, A, Nagashima, Y, Shimada, H & Miyazaki, K (2000). Marked increase of trypsin(ogen) in serum of linitis plastica (gastric cancer, borrmann 4) patients [In Process Citation]. Clin Cancer Res, 6, 1385–1388.
Ishihara, H, Connolly, AJ, Zeng, D, Kahn, ML, Zheng, YW, Timmons, C, Tram, T & Coughlin, SR (1997). Protease-activated receptor 3 is a second thrombin receptor in humans. Nature, 386, 502–506.
Kawano, N, Osawa, H, Ito, T, Nagashima, Y, Hirahara, F, Inayama, Y, Nakatani, Y, Kimura, S, Kitajima, H, Koshikawa, N, Miyazaki, K & Kitamura, H (1997). Expression of gelatinase A, tissue inhibitor of metalloproteinases-2, matrilysin, and trypsin(ogen) in lung neoplasms: an immunohistochemical study. Hum Pathol, 28, 613–622.
Kennedy, AR (1994). Prevention of carcinogenesis by protease inhibitors. Cancer Res, 54, 1999s–2005s.
Kennedy, AR (1998). The Bowman-Birk inhibitor from soybeans as an anticarcinogenic agent. Am J Clin Nutr, 68, 1406s–1412s.
Kong, W, McConalogue, K, Khitin, LM, Hollenberg, MD, Payan, DG, Bohm, SK & Bunnett, NW (1997). Luminal trypsin may regulate enterocytes through proteinase-activated receptor 2. Proc Natl Acad Sci USA, 94, 8884–8889.
Koshikawa, N, Hasegawa, S, Nagashima, Y, Mitsuhashi, K, Tsubota, Y, Miyata, S, Miyagi, Y, Yasumitsu, H & Miyazaki, K (1998). Expression of trypsin by epithelial cells of various tissues, leukocytes, and neurons in human and mouse. Am J Pathol, 153, 937–944.
Koshikawa, N, Nagashima, Y, Miyagi, Y, Mizushima, H, Yanoma, S, Yasumitsu, H & Miyazaki, K (1997). Expression of trypsin in vascular endothelial cells. FEBS Lett, 409, 442–448.
Koshikawa, N, Yasumitsu, H, Umeda, M & Miyazaki, K (1992). Multiple secretion of matrix serine proteinases by human gastric carcinoma cell lines. Cancer Res, 52, 5046–5053.
Laburthe, M, Rousset, M, Rouyer-Fessard, C, Couvineau, A, Chantret, I, Chevalier, G & Zweibaum, A (1987). Development of vasoactive intestinal peptide-responsive adenylate cyclase during enterocytic differentiation of Caco-2 cells in culture. Evidence for an increased receptor level. J Biol Chem, 262, 10180–10184.
Maoret, JJ, Anini, Y, Rouyer-Fessard, C, Gully, D & Laburthe, M (1999). Neurotensin and a non-peptide neurotensin receptor antagonist control human colon cancer cell growth in cell culture and in cells xenografted into nude mice. Int J Cancer, 80, 448–454.
Mazzieri, R, Masiero, L, Zanetta, L, Monea, S, Onisto, M, Garbisa, S & Mignatti, P (1997). Control of type IV collagenase activity by components of the urokinase-plasmin system: a regulatory mechanism with cell-bound reactants. EMBO J, 16, 2319–2332.
McCawley, LJ & Matrisian, LM (2000). Matrix metalloproteinases: multifunctional contributors to tumor progression. Mol Med Today, 6, 149–156.
Mignatti, P & Rifkin, DB (1993). Biology and biochemistry of proteinases in tumor invasion. Physiol Rev, 73, 161–195.
Mirza, H, Schmidt, VA, Derian, CK, Jesty, J & Bahou, WF (1997). Mitogenic responses mediated through the proteinase-activated receptor-2 are induced by expressed forms of mast cell alpha-or beta-tryptases. Blood, 90, 3914–3922.
Miyata, S, Koshikawa, N, Higashi, S, Miyagi, Y, Nagashima, Y, Yanoma, S, Kato, Y, Yasumitsu, H & Miyazaki, K (1999). Expression of trypsin in human cancer cell lines and cancer tissues and its tight binding to soluble form of Alzheimer amyloid precursor protein in culture. J Biochem (Tokyo), 125, 1067–1076.
Miyata, S, Miyagi, Y, Koshikawa, N, Nagashima, Y, Kato, Y, Yasumitsu, H, Hirahara, F, Misugi, K & Miyazaki, K (1998). Stimulation of cellular growth and adhesion to fibronectin and vitronectin in culture and tumorigenicity in nude mice by overexpression of trypsinogen in human gastric cancer cells. Clin Exp Metastasis, 16, 613–622.
Molino, M, Barnathan, ES, Numerof, R, Clark, J, Dreyer, M, Cumashi, A, Hoxie, JA, Schechter, N, Woolkalis, M & Brass, LF (1997a). Interactions of mast cell tryptase with thrombin receptors and PAR-2. J Biol Chem, 272, 4043–4049.
Molino, M, Raghunath, PN, Kuo, A, Ahuja, M, Hoxie, JA, Brass, LF & Barnathan, ES (1998). Differential expression of functional protease-activated receptor-2 (PAR-2) in human vascular smooth muscle cells. Arterioscler Thromb Vasc Biol, 18, 825–832.
Molino, M, Woolkalis, MJ, Reavey-Cantwell, J, Pratico, D, Andrade-Gordon, P, Barnathan, ES & Brass, LF (1997b). Endothelial cell thrombin receptors and PAR-2. Two protease-activated receptors located in a single cellular environment. J Biol Chem, 272, 11133–11141.
Nguyen, TD, Moody, MW, Steinhoff, M, Okolo, C, Koh, DS & Bunnett, NW (1999). Trypsin activates pancreatic duct epithelial cell ion channels through proteinase-activated receptor-2. J Clin Invest, 103, 261–269.
Normanno, N, De Luca, A, Salomon, DS & Ciardiello, F (1998). Epidermal growth factor-related peptides as targets for experimental therapy of human colon carcinoma. Cancer Detect Prev, 22, 62–67.
Nystedt, S, Emilsson, K, Larsson, AK, Strombeck, B & Sundelin, J (1995). Molecular cloning and functional expression of the gene encoding the human proteinase-activated receptor 2. Eur J Biochem, 232, 84–89.
Nystedt, S, Emilsson, K, Wahlestedt, C & Sundelin, J (1994). Molecular cloning of a potential proteinase activated receptor. Proc Natl Acad Sci USA, 91, 9208–9212.
O’Brien, PJ, Molino, M, Kahn, M & Brass, LF (2001). Protease activated receptors: theme and variations. Oncogene, 20, 1570–1581.
Ramos-DeSimone, N, Hahn-Dantona, E, Sipley, J, Nagase, H, French, DL & Quigley, JP (1999). Activation of matrix metalloproteinase-9 (MMP-9) via a converging plasmin/stromelysin-1 cascade enhances tumor cell invasion. J Biol Chem, 274, 13066–13076.
Saifeddine, M, al-Ani, B, Cheng, CH, Wang, L & Hollenberg, MD (1996). Rat proteinase-activated receptor-2 (PAR-2): cDNA sequence and activity of receptor-derived peptides in gastric and vascular tissue. Br J Pharmacol, 118, 521–530.
Singh, P & Rubin, N (1993). Insulinlike growth factors and binding proteins in colon cancer. Gastroenterology, 105, 1218–1237.
Singh, P, Velasco, M, Given, R, Wargovich, M, Varro, A & Wang, TC (2000). Mice overexpressing progastrin are predisposed for developing aberrant colonic crypt foci in response to AOM. Am J Physiol Gastrointest Liver Physiol, 278, G390–G399.
Smith, R, Jenkins, A, Lourbakos, A, Thompson, P, Ramakrishnan, V, Tomlinson, J, Deshpande, U, Johnson, DA, Jones, R, Mackie, EJ & Pike, RN (2000). Evidence for the activation of PAR-2 by the sperm protease, acrosin: expression of the receptor on oocytes. FEBS Lett, 484, 285–290.
Sorsa, T, Salo, T, Koivunen, E, Tyynela, J, Konttinen, YT, Bergmann, U, Tuuttila, A, Niemi, E, Teronen, O, Heikkila, P, Tschesche, H, Leinonen, J, Osman, S & Stenman, UH (1997). Activation of type IV procollagenases by human tumor-associated trypsin-2. J Biol Chem, 272, 21067–21074.
Vergnolle, N (2000). Review article: proteinase-activated receptors – novel signals for gastrointestinal pathophysiology. Aliment Pharmacol Ther, 14, 257–266.
Vergnolle, N, Macnaughton, WK, Al-Ani, B, Saifeddine, M, Wallace, JL & Hollenberg, MD (1998). Proteinase-activated receptor 2 (PAR2)-activating peptides: identification of a receptor distinct from PAR2 that regulates intestinal transport. Proc Natl Acad Sci USA, 95, 7766–7771.
Vu, TK, Hung, DT, Wheaton, VI & Coughlin, SR (1991). Molecular cloning of a functional thrombin receptor reveals a novel proteolytic mechanism of receptor activation. Cell, 64, 1057–1068.
Xu, WF, Andersen, H, Whitmore, TE, Presnell, SR, Yee, DP, Ching, A, Gilbert, T, Davie, EW & Foster, DC (1998). Cloning and characterization of human protease-activated receptor 4. Proc Natl Acad Sci USA, 95, 6642–6646.
Yu, Z, Ahmad, S, Schwartz, JL, Banville, D & Shen, SH (1997). Protein-tyrosine phosphatase SHP2 is positively linked to proteinase-activated receptor 2-mediated mitogenic pathway. J Biol Chem, 272, 7519–7524.
Zweibaum, A, Laburthe, M, Grasset, E & Louvard, D (1991). The gastrointestinal system: Intestinal absorption and secretion. Field M, Frizzell RA (eds) Vol IV, 223–255, American Physiological Society: Bethesda, MD, USA
Author information
Authors and Affiliations
Rights and permissions
From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
About this article
Cite this article
Darmoul, D., Marie, JC., Devaud, H. et al. Initiation of human colon cancer cell proliferation by trypsin acting at protease-activated receptor-2. Br J Cancer 85, 772–779 (2001). https://doi.org/10.1054/bjoc.2001.1976
Received:
Revised:
Accepted:
Published:
Issue date:
DOI: https://doi.org/10.1054/bjoc.2001.1976
Keywords
This article is cited by
-
Natural bio-based monomers for biomedical applications: a review
Biomaterials Research (2021)
-
Best practices for naming, receiving, and managing cells in culture
In Vitro Cellular & Developmental Biology - Animal (2017)
-
ARNTL2 and SERPINE1: potential biomarkers for tumor aggressiveness in colorectal cancer
Journal of Cancer Research and Clinical Oncology (2012)
-
Protease-activated receptor-2 regulates cyclooxygenase-2 expression in human bile duct cancer via the pathways of mitogen-activated protein kinases and nuclear factor kappa B
Journal of Hepato-Biliary-Pancreatic Sciences (2011)
-
Expression of Protease Activated Receptor-2 in Human Colorectal Cancer and Its Association With Tumor Progression
Diseases of the Colon & Rectum (2010)


