교수진 소개
김철호 Ph.D.
교수 [겸직교수]
2020~현재
일본국 후쿠오카 쥰신 대학교 비상근 교수
2015~2016
미국 오하이오 주립대학 Functional Genomics 객원교수
2010~현재
The Peer Journal, Int J Molec Sci 편집위원
2010~현재
Frontiers in Pharmacology 및 eCAM 부편집위원, Current Pharm. Biotechnol 공동편집위원장
2010~2011
일본국 토카이 대학교 당쇄과학연구소 객원교수
2006~현재
성균관대학교 생명과학과 교수, 삼성융합의과학원 교수, 학과장
1996~2006
동국대학교 한의과대학 생화학교실 조교수, 부교수, 정교수, 주임교수, 한의학과장
1990~1996
한국과학기술연구원 유전공학센터, 현재 한국생명공학연구원 분자생물학실 선임연구원 및 게놈연구담당 실장
1990
동경대학 대학원 석사 및 박사
1987~1989
일본국 동경의약대학 생물공학과 비상근강사
Research interests are the field of glycomics and glycobiology, expecially on sphingolipid, ceramide and sialic acid-containing sphingolipids, ganglioside. Academic findings: Hepatic B Viral hepatocarcinoma and PTEN (Cancer Res 2003), asialo-1 acid glycoprotein in liver cirrhosis and carcinoma (Hepatol Res, 2003), GlcNAc:βMan1,4GlcNAcT-III in hepatitis (Glycoconj J, 2003), MMP-9/2 and α-fetoproteins in HBV hepatitis (J. Gastroent Hepatol 2004), HBV metastatic (FASEB J. 2004), Hepatic GnT-V and GnT-III-ApoB100 (JBC. 2004), Disialo GD3 in VSMC (JBC. 2004), therapeutic hepatocarcinoma cells (FASEB J. 2004), TG-2 in leukemia (FEBS Lett. 2004), N-GlcNAcT-III in HBV (J Gastroent Hepatol, 2004), Monosialyl GM3 in leukemic differentiation (Glycobiology 2005), MMP-9 in IVF (British J Obstetrics and Gynecol. 2005), disialo GD3 Fas-T cells (Glycobiology 2006), GM3 in PTEN (Glycobiology 2006), ROS in sialic GD3-cell (FASEB J 2006), AP-2a in GM3-PTEN (Glycobiology 2008), sialidase in leukemia (BBA 2008), GM3-VEGFR-2 interaction (Glycobiology 2009), GD3 in breast cancer (Biological Chemistry 2009), pig CMAH and N-glycolylneuraminic acid (Biochem J 2010), pST6GalNAc IV for Neu5Aca2-3Galb1-3GalNAc (Glycoconj J 2011), GM3 in TGF-β1-induced EMT (Biochem J. 2013), VEGFR-2 in neovascularization (J Mol Medicine 2013), monosialyl GM3 (Plos One 2014) and TGF-receptor (Int. J. of Biochem. Cell Biol. 2014), Sialyl Le A/X of HBx (Mol Cancer 2014, J Cell Biochem 2015). Housekeeping promoter 5'pcmah-2 of CMP-NeuGc gene (Glycoconj 2016), GD1b Apoptosis of MCF-7 (IJMS 2016), Human ST8Sia VI (α2,8-Sialyltransferase) Gene (IJMS 2016), GD2-ICAMI (IJMS 2017), Sialyllactose VEGFR-2 activation, GD3/a1AR/TG2, AApoB100-GM3, GM3-macrophage (JCB, 2017, 2018), Sirt1-FcεRI- mast cell AMPK (Sci Rep, 2017), ASC/LPS (PloS One 2017), 4-o-cASC (JCB, JSMB 2018), SARS-CoV-2-sialylation. Lectin-Glycan (IJMS, 2020),CMP-NeuGc (Sci Rep 2019), AC (FP), 3-SL-sIGLEC (Glycoconj J 2020), Avc(FP, 2021, IJMS 2021)
분자세포당생물학
1. (2024) Compared Inhibitory Activities of Tamoxifen and Avenanthramide B on Liver Esterase and Correlation Based on the Superimposed Structure Between Porcine and Human Liver Esterase. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 25, 24
2. (2024) Human ST3Gal II and ST6GalNAc IV genes increase human serum-mediated cytotoxicity to xenogeneic cells. XENOTRANSPLANTATION. 31, 12855
3. (2024) Dawn era for revisited cancer therapy by innate immune system and immune checkpoint inhibitors. Biochimica et Biophysica Acta - Molecular Basis of Disease. 1870, 3
4. (2024) A novel Mycobacterium Tuberculosis antigen, MTB48 enhances inflammatory response in LPS-induced RAW264.7 macrophage immune cells. MOLECULAR IMMUNOLOGY. 166, 2
5. (2024) 5-methylthiopentyl Isothiocyanate, a Sulforaphane Analogue, Inhibits Pro-inflammatory Cytokines by Regulating LPS/ATP-mediated NLRP3 Inflammasome Activation. CURRENT PHARMACEUTICAL BIOTECHNOLOGY. 25, 5