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RAGE, carboxylated glycans and S100A8/A9 play essential roles in colitis-associated carcinogenesis.

Turovskaya O, Foell D, Sinha P, Vogl T, Newlin R, Nayak J, Nguyen M, Olsson A, Nawroth PP, Bierhaus A, Varki N, Kronenberg M, Freeze HH, Srikrishna G.

Carcinogenesis. 2008 Oct;29(10):2035-43. doi: 10.1093/carcin/bgn188. Epub 2008 Aug 9.


S100A8/A9 activate key genes and pathways in colon tumor progression.

Ichikawa M, Williams R, Wang L, Vogl T, Srikrishna G.

Mol Cancer Res. 2011 Feb;9(2):133-48. doi: 10.1158/1541-7786.MCR-10-0394. Epub 2011 Jan 12. Erratum in: Mol Cancer Res. 2011 Sep;9(9):1266.


S100A8/A9 aggravates post-ischemic heart failure through activation of RAGE-dependent NF-κB signaling.

Volz HC, Laohachewin D, Seidel C, Lasitschka F, Keilbach K, Wienbrandt AR, Andrassy J, Bierhaus A, Kaya Z, Katus HA, Andrassy M.

Basic Res Cardiol. 2012 Mar;107(2):250. doi: 10.1007/s00395-012-0250-z. Epub 2012 Feb 10.


Proinflammatory S100 proteins regulate the accumulation of myeloid-derived suppressor cells.

Sinha P, Okoro C, Foell D, Freeze HH, Ostrand-Rosenberg S, Srikrishna G.

J Immunol. 2008 Oct 1;181(7):4666-75.


S100A8/A9 at low concentration promotes tumor cell growth via RAGE ligation and MAP kinase-dependent pathway.

Ghavami S, Rashedi I, Dattilo BM, Eshraghi M, Chazin WJ, Hashemi M, Wesselborg S, Kerkhoff C, Los M.

J Leukoc Biol. 2008 Jun;83(6):1484-92. doi: 10.1189/jlb.0607397. Epub 2008 Mar 13.


Carboxylated glycans mediate colitis through activation of NF-kappa B.

Srikrishna G, Turovskaya O, Shaikh R, Newlin R, Foell D, Murch S, Kronenberg M, Freeze HH.

J Immunol. 2005 Oct 15;175(8):5412-22.


RAGE-binding S100A8/A9 promotes the migration and invasion of human breast cancer cells through actin polymerization and epithelial-mesenchymal transition.

Yin C, Li H, Zhang B, Liu Y, Lu G, Lu S, Sun L, Qi Y, Li X, Chen W.

Breast Cancer Res Treat. 2013 Nov;142(2):297-309. doi: 10.1007/s10549-013-2737-1. Epub 2013 Nov 1.


S100A8 and S100A9 promotes invasion and migration through p38 mitogen-activated protein kinase-dependent NF-κB activation in gastric cancer cells.

Kwon CH, Moon HJ, Park HJ, Choi JH, Park do Y.

Mol Cells. 2013 Mar;35(3):226-34. doi: 10.1007/s10059-013-2269-x. Epub 2013 Feb 26.


Carboxylated N-glycans on RAGE promote S100A12 binding and signaling.

Srikrishna G, Nayak J, Weigle B, Temme A, Foell D, Hazelwood L, Olsson A, Volkmann N, Hanein D, Freeze HH.

J Cell Biochem. 2010 Jun 1;110(3):645-59. doi: 10.1002/jcb.22575. Erratum in: J Cell Biochem. 2010 Sep 1;111(1):248.


Proinflammatory Proteins S100A8/S100A9 Activate NK Cells via Interaction with RAGE.

Narumi K, Miyakawa R, Ueda R, Hashimoto H, Yamamoto Y, Yoshida T, Aoki K.

J Immunol. 2015 Jun 1;194(11):5539-48. doi: 10.4049/jimmunol.1402301. Epub 2015 Apr 24.


HaCaT keratinocytes overexpressing the S100 proteins S100A8 and S100A9 show increased NADPH oxidase and NF-kappaB activities.

Benedyk M, Sopalla C, Nacken W, Bode G, Melkonyan H, Banfi B, Kerkhoff C.

J Invest Dermatol. 2007 Aug;127(8):2001-11. Epub 2007 Apr 12.


RAGE-dependent regulation of calcium-binding proteins S100A8 and S100A9 in human THP-1.

Eggers K, Sikora K, Lorenz M, Taubert T, Moobed M, Baumann G, Stangl K, Stangl V.

Exp Clin Endocrinol Diabetes. 2011 Jun;119(6):353-7. doi: 10.1055/s-0030-1268426. Epub 2011 Apr 6.


Two proteins modulating transendothelial migration of leukocytes recognize novel carboxylated glycans on endothelial cells.

Srikrishna G, Panneerselvam K, Westphal V, Abraham V, Varki A, Freeze HH.

J Immunol. 2001 Apr 1;166(7):4678-88.


The role of myofibroblasts in upregulation of S100A8 and S100A9 and the differentiation of myeloid cells in the colorectal cancer microenvironment.

Kim JH, Oh SH, Kim EJ, Park SJ, Hong SP, Cheon JH, Kim TI, Kim WH.

Biochem Biophys Res Commun. 2012 Jun 22;423(1):60-6. doi: 10.1016/j.bbrc.2012.05.081. Epub 2012 May 22.


S100A8 and S100A9 activate MAP kinase and NF-kappaB signaling pathways and trigger translocation of RAGE in human prostate cancer cells.

Hermani A, De Servi B, Medunjanin S, Tessier PA, Mayer D.

Exp Cell Res. 2006 Jan 15;312(2):184-97. Epub 2005 Nov 17.


N -Glycans on the receptor for advanced glycation end products influence amphoterin binding and neurite outgrowth.

Srikrishna G, Huttunen HJ, Johansson L, Weigle B, Yamaguchi Y, Rauvala H, Freeze HH.

J Neurochem. 2002 Mar;80(6):998-1008.


S100A8 and S100A9 mediate endotoxin-induced cardiomyocyte dysfunction via the receptor for advanced glycation end products.

Boyd JH, Kan B, Roberts H, Wang Y, Walley KR.

Circ Res. 2008 May 23;102(10):1239-46. doi: 10.1161/CIRCRESAHA.107.167544. Epub 2008 Apr 10.


S100a8/a9 released by CD11b+Gr1+ neutrophils activates cardiac fibroblasts to initiate angiotensin II-Induced cardiac inflammation and injury.

Wu Y, Li Y, Zhang C, A X, Wang Y, Cui W, Li H, Du J.

Hypertension. 2014 Jun;63(6):1241-50. doi: 10.1161/HYPERTENSIONAHA.113.02843. Epub 2014 Apr 7.


Increased proinflammatory endothelial response to S100A8/A9 after preactivation through advanced glycation end products.

Ehlermann P, Eggers K, Bierhaus A, Most P, Weichenhan D, Greten J, Nawroth PP, Katus HA, Remppis A.

Cardiovasc Diabetol. 2006 Mar 30;5:6.


Smad4 loss is associated with fewer S100A8-positive monocytes in colorectal tumors and attenuated response to S100A8 in colorectal and pancreatic cancer cells.

Ang CW, Nedjadi T, Sheikh AA, Tweedle EM, Tonack S, Honap S, Jenkins RE, Park BK, Schwarte-Waldhoff I, Khattak I, Azadeh B, Dodson A, Kalirai H, Neoptolemos JP, Rooney PS, Costello E.

Carcinogenesis. 2010 Sep;31(9):1541-51. doi: 10.1093/carcin/bgq137. Epub 2010 Jul 9.

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