Contact: Charles University, Faculty of Pharmacy in Hradec Kralove, Department of Pharmacology and Toxicology, Czech Republic
Tel: +420 495 067 593
Email: jakub.hofman@faf.cuni.cz
| 2014 - 2015 | a six-month research stay in Institut für Toxikologie und Pharmakologie für Naturwissenschaftler, Kiel, Germany (group of Prof. Dr. Edmund Maser) |
| 2008 - 2012 |
doctoral study (Ph.D. in pharmacology and toxicology; RNDr. in biochemistry) |
| 2005-2007 |
master study (M.Sc. in biochemistry) |
| 2002 - 2005 |
bachelor study (B.Sc. in biochemistry) |
| 2007 - 2008 |
EMPLA s r.o. |
| 2008 - 2012 |
GENERI BIOTECH s r.o. |
| 2012 - 2015 |
Charles University in Prague, Faculty of Pharmacy in Hradec Kralove, Department of Biochemical Sciences |
| 2015 - 2021 |
Charles University in Prague, Faculty of Pharmacy in Hradec Kralove, Department of Pharmacology and Toxicology |
| 2021 - present | Charles University in Prague, Faculty of Pharmacy in Hradec Kralove, Department of Pharmacology and Toxicology position: associate professor |
| 2022 - present | lecturer of Pharmacology |
| 2017 - present | lecturer of Current strategies in pharmacotherapy |
| 2017 - present | lecturer of Pharmacokinetics |
| 2016 - present | lecturer of Pharmacology seminars |
| 2013 - 2015 | lecturer of Practical courses in general biochemistry |
| 2013 - present | supervisor of 24 M.Sc. students during their master thesis |
| 2020 - present | supervisor of 6 Ph.D. students (4 graduated) |
h-index = 16, 585 citations (excluding self-citations; 17th April 2025)
Hofman J., Skarka A., Havrankova J., Wsol V.: Pharmacokinetic interactions of breast cancer chemotherapeutics with human doxorubicin reductases. Biochem Pharmacol 2015; 96 (3): 168 - 78 (IF for 2015 = 5.091)
Hofman J., Kučera R., Neumanova Z., Klimes J., Ceckova M., Staud F.: Placental passage of olomoucine II, but not purvalanol A, is affected by p-glycoprotein (ABCB1), breast cancer resistance protein (ABCG2) and multidrug resistance-associated proteins (ABCCs). Xenobiotica 2016; 46(5): 416-23 (IF for 2016 = 1.932).
Zemanova L., Hofman J., Novotna E., Musilek K., Lundova T., Havrankova J., Hostalkova A., Chlebek J., Cahlikova L., Wsol V.: Flavones Inhibit the Activity of AKR1B10, a Promising Therapeutic Target for Cancer Treatment. J Nat Prod 2015; 78 (11): 2666 - 74 (IF for 2015 = 3.662)
Hintzpeter J., Seliger J.M., Hofman J., Martin H.J., Wsol V., Maser E.: Inhibition of human anthracycline reductases by emodin - a possible remedy for anthracycline resistance. Toxicol Appl Pharmacol 2016; 293: 21-9 (IF for 2016 = 3.791)
Siroka J., Ceckova M., Urbanek L., Krystof V., Gucky T., Hofman J., Strnad M., Staud F.: LC-MS/MS method for determination of cyclin-dependent kinase inhibitors, BP-14 and BP-20, and its application in pharmacokinetic study in rat. J Chromatogr B Analyt Technol Biomed Life Sci 2018; 1089: 24-32 (IF for 2018 = 2.813)
Sorf A., Hofman J, Kucera R., Staud F., Ceckova M.: Ribociclib shows potential for pharmacokinetic drug-drug interactions being a substrate of ABCB1 and potent inhibitor of ABCB1, ABCG2 and CYP450 isoforms in vitro. Biochem Pharmacol 2018; 154: 10-7 (IF for 2018 = 4.825)
Novotna E., Büküm N., Hofman J., Flaxova M., Kouklikova E., Louvarova D., Wsol V.: Aldo-keto reductase 1C3 (AKR1C3): a missing piece of the puzzle in the dinaciclib interaction profile. Arch Toxicol 2018; 92: 2845-2857 (IF for 2018 = 5.741)
Novotna E., Büküm N., Hofman J., Flaxova M., Kouklikova E., Louvarova D., Wsol V.: Roscovitine and purvalanol A effectively reverse anthracycline resistance mediated by the activity of aldo-keto reductase 1C3 (AKR1C3). Biochem Pharmacol 2018; 156: 22-31 (IF for 2018 = 4.825)
Büküm N., Novotna E., Morell A., Hofman J., Wsol V.: Buparlisib is a novel inhibitor of daunorubicin reduction mediated by aldo-keto reductase 1C3. Chem Biol Interact 2019; 302: 101-7 (IF for 2019 = 3.723)
Sorf A., Novotna E., Hofman J., Morell A., Staud F., Wsol V., Ceckova M.: Cyclin-dependent kinase inhibitors AZD5438 and R547 show potential for enhancing efficacy of daunorubicin-based anticancer therapy: Interaction with carbonyl-reducing enzymes and ABC transporters. Biochem Pharmacol 2019; 163: 290-8 (IF for 2019 = 4.960)
Sabet Z., Vagiannis D., Budagaga Y., Zhang Y., Novotná E., Hanke I., Rozkoš T., Hofman J.: Talazoparib Does Not Interact with ABCB1 Transporter or Cytochrome P450s, but Modulates Multidrug Resistance Mediated by ABCC1 and ABCG2: An in Vitro and Ex Vivo Study. Int J Mol Sci 2022; 23(22): 14338 (IF for 2022/2023 = 5.6)
Zhang Y., Vagiannis D., Budagaga Y., Sabet Z., Hanke I., Rozkoš T., Hofman J.: Encorafenib Acts as a Dual-Activity Chemosensitizer through Its Inhibitory Effect on ABCC1 Transporter In Vitro and Ex Vivo. Pharmaceutics 2022; 14(12): 2595 (IF for 2022/2023 = 5.4)
Budagaga Y., Sabet Z., Zhang Y., Novotná E., Hanke I., Rozkoš T., Hofman J.: Tazemetostat synergistically combats multidrug resistance by the unique triple inhibition of ABCB1, ABCC1, and ABCG2 efflux transporters in vitro and ex vivo. Biochem Pharmacol 2023;216:115769 (IF for 2022/2023 = 5.8)