Mukerrem Betul Yerer-Aycan is a pharmacist, physiologist and an Assoc.Prof. in the fi eld of Pharmacology working in the Erciyes University, Faculty of Pharmacy, Dept. of Pharmacology, Turkey. She is the Chair of the Department since 2007 and the Vice-Dean of the Faculty since 2008. She has studied some parts of her PhD thesis in Spain in 2005 and did her post doc in Switzerland in 2007 and visited Colorado University, Denver, US for a while in 2011 to conduct a common research project. She has 14 papers in SCI and more than 15 national papers and more than 50 presentations in around 30 meetings. She has completed nearly 20 national or international projects from 2005 up to date. She has been awarded nationally or internationally 15 times for her several studies. She is the team leader of 2 MSc and 6 PhD students now and they are recentlyworking on the anticancerogen effects of some natural products. She is in the editorial board of Current Pharmacogenomics and Personalized Medicine and she is an offi cial member of 10 scientifi c societies. She says the biggest due of her career is ‘she is the mother of two sons’.


Drug discovery and development is both time and resource-intensive endeavor which is not always guaranteed to result in safe and effi cacious drugs. Th e eff ective concentration of the compound and importantly the time needed for the compound to perturb the target varies from one compound to another. Taking into account those diff erences and limitations, we used a real time cell analyser that reveals the real time eff ects of the compounds over the impedence alterations on the e-plates. We tested extracts of some natural compounds such as Salvia species, Chrisophtalmum species, Zizyphus species etc., and some natural basic compounds such as gallicasid, ferulic acid, apigenin, luteolin, quercetin, curcumin etc. On several cell lines such as HepG2, A549, SHSY5Y, Colo 205 and Beta TC-6. Th e impedence profi le and the time needed for the coumpound to interact with the cells varied from compound to compund and from cell to cell. We found that some natural compounds with similar biological activity produced similar impedance-based time-dependent cell response profi les (TCRP) as similar to results described over around 2000 chemical compounds before. Due to the kinetic nature of the profi ling approach both short term and long term compound activity can be measured, allowing to guess the probable targets of the compounds on diff erent cell lines. For instance, according to the results of this study the similar compounds showing their eff ects over DNA methylation, PPAR antagonism, cycline dependent kinase inhibition, Ca channel inhibition, tubulin polymerisation, apoptosis or cytotxicity have similar TCRPs with the real time cell analyser. In our study, we observed similar results with the natural compound extracts or basic natural compounds. Th ese fi ndings indicate that using impedance-based monitoring and profi ling of cellular response upon exposure to biologically active compounds can provide incisive and quantitative information to novel mechanisms for these natural compounds.