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Blockade of Wnt-1 signaling induces apoptosis in human colorectal cancer cells containing downstream mutations

Abstract

Aberrant Wnt signaling, mainly through mutations of APC and in some cases of CTNNB1 or AXIN2, has been found in the majority of colorectal cancers. Recently, frequent promoter hypermethylation was identified to cause silencing of the secreted frizzled-related protein (sFRP) family in colorectal cancer. Restoration of sFRP in colorectal cancer cells attenuates Wnt signaling even in the presence of downstream mutations. Here we show that Wnt inhibitory factor-1 (WIF-1), a different secreted antagonist of Wnt signaling, is also silenced by promoter hypermethylation in colorectal cancer cells. Restoration of WIF-1 function, Wnt-1 siRNA, or a monoclonal anti-Wnt-1 antibody that we developed attenuates Wnt-1 signaling and induces significant apoptosis in these cells containing downstream mutations and expressing Wnt-1. In addition, this monoclonal anti-Wnt-1 antibody showed synergistic effects with docetaxel in treating these colorectal cancer cells and great efficacy in treating primary colorectal cancer cultures freshly prepared from patients. Therefore, our data support the hypothesis that constitutive Wnt signaling may be required to complement downstream mutations in the evolution of colorectal cancer. Furthermore, our results suggest that blockade of the Wnt signal may have a therapeutic role in the treatment of colorectal cancer.

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References

  • Bissery MC, Guenard D, Gueritte-Voegelein F and Lavelle F . (1991). Cancer Res, 51, 4845–4852.

  • Caldwell GM, Jones C, Gensberg K, Jan S, Hardy RG, Byrd P, Chughtai S, Wallis Y, Matthews GM and Morton DG . (2004). Cancer Res., 64, 883–888.

  • Ciani L, Krylova O, Smalley MJ, Dale TC and Salinas PC . (2004). J. Cell Biol., 164, 243–253.

  • Clark TB, Kemeny NE, Conti JA, Huang Y, Andre AM and Stockman J . (1998). Cancer Invest., 16, 314–318.

  • Dimitriadis A, Vincan E, Mohammed IM, Roczo N, Phillips WA and Baindur-Hudson S . (2001). Cancer Lett., 166, 185–191.

  • Dunne AL, Mothersill C, Robson T, Wilson GD and Hirst DG . (2004). Oncol. Res., 14, 447–454.

  • Elbashir SM, Harborth J, Weber K and Tuschl T . (2002). Methods, 26, 199–213.

  • Fodde R, Smits R and Clevers H . (2001). Nat. Rev. Cancer, 1, 55–67.

  • Giles RH, van Es JH and Clevers H . (2003). Biochim. Biophys. Acta, 1653, 1–24.

  • He B, You L, Uematsu K, Xu Z, Lee AY, Matsangou M, McCormick F and Jablons DM . (2004). Neoplasia, 6, 7–14.

  • He B, You L, Uematsu K, Zang K, Xu Z, Lee AY, Costello JF, McCormick F and Jablons DM . (2003). Proc. Natl. Acad. Sci. USA, 100, 14133–14138.

  • Heighway J, Knapp T, Boyce L, Brennand S, Field JK, Betticher DC, Ratschiller D, Gugger M, Donovan M, Lasek A and Rickert P . (2002). Oncogene, 21, 7749–7763.

  • Holcombe RF, Marsh JL, Waterman ML, Lin F, Milovanovic T and Truong T . (2002). Mol. Pathol., 55, 220–226.

  • Hsieh JC, Kodjabachian L, Rebbert ML, Rattner A, Smallwood PM, Samos CH, Nusse R, Dawid IB and Nathans J . (1999). Nature, 398, 431–436.

  • Karantanis E, Nicholson S and Morris DL . (1994). Eur. J. Surg. Oncol., 20, 653–657.

  • Kawano Y and Kypta R . (2003). J. Cell Sci., 116, 2627–2634.

  • Kim PJ, Plescia J, Clevers H, Fearon ER and Altieri DC . (2003). Lancet, 362, 205–209.

  • Korinek V, Barker N, Morin PJ, van Wichen D, de Weger R, Kinzler KW, Vogelstein B and Clevers H . (1997). Science, 275, 1784–1787.

  • Lin K, Wang S, Julius MA, Kitajewski J, Moos Jr M and Luyten FP . (1997). Proc. Natl. Acad. Sci. USA, 94, 11196–11200.

  • Liu W, Dong X, Mai M, Seelan RS, Taniguchi K, Krishnadath KK, Halling KC, Cunningham JM, Boardman LA, Qian C, Christensen E, Schmidt SS, Roche PC, Smith DI and Thibodeau SN . (2000). Nat. Genet., 26, 146–147.

  • Mazieres J, He B, You L, Xu Z, Lee A, Mikami I, Reguart N, Rosell R, McCormick F and Jablons DM . (2004). Cancer Res., 64, 4717–4720.

  • Morin PJ, Sparks AB, Korinek V, Barker N, Clevers H, Vogelstein B and Kinzler KW . (1997). Science, 275, 1787–1790.

  • Smith K, Bui TD, Poulsom R, Kaklamanis L, Williams G and Harris AL . (1999). Br. J. Cancer, 81, 496–502.

  • Sternberg CN, ten Bokkel Huinink WW, Smyth JF, Bruntsch V, Dirix LY, Pavlidis NA, Franklin H, Wanders S, Le Bail N and Kaye SB . (1994). Br. J. Cancer, 70, 376–379.

  • Suzuki H, Gabrielson E, Chen W, Anbazhagan R, van Engeland M, Weijenberg MP, Herman JG and Baylin SB . (2002). Nat. Genet., 31, 141–149.

  • Suzuki H, Watkins DN, Jair KW, Schuebel KE, Markowitz SD, Dong Chen W, Pretlow TP, Yang B, Akiyama Y, Van Engeland M, Toyota M, Tokino T, Hinoda Y, Imai K, Herman JG and Baylin SB . (2004). Nat. Genet., 36, 417–422.

  • Taketo MM . (2004). Nat. Genet., 36, 320–322.

  • Veeman MT, Axelrod JD and Moon RT . (2003). Dev. Cell, 5, 367–377.

  • Wissmann C, Wild PJ, Kaiser S, Roepcke S, Stoehr R, Woenckhaus M, Kristiansen G, Hsieh JC, Hofstaedter F, Hartmann A, Knuechel R, Rosenthal A and Pilarsky C . (2003). J. Pathol., 201, 204–212.

  • You L, He B, Xu Z, Uematsu K, Mazieres J, Fujii N, Mikami I, Reguart N, McIntosh JK, Kashani-Sabet M, McCormick F and Jablons DM . (2004). Cancer Res., 64, 5385–5389.

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Acknowledgements

This work was supported by the Larry Hall memorial trust and the Kazan, McClain, Edises, Abrams, Fernandez, Lyons & Farrise Foundation.

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Correspondence to David M Jablons.

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He, B., Reguart, N., You, L. et al. Blockade of Wnt-1 signaling induces apoptosis in human colorectal cancer cells containing downstream mutations. Oncogene 24, 3054–3058 (2005). https://doi.org/10.1038/sj.onc.1208511

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