Cancer cells response on the microtubuler-inhibiting drugs

dc.contributor.authorBalabiyev, A.
dc.contributor.authorKakpenova, A.
dc.contributor.authorKauanova, S.
dc.contributor.authorVorobjev, I.A.
dc.date.accessioned2016-05-30T08:21:42Z
dc.date.available2016-05-30T08:21:42Z
dc.date.issued2016-05
dc.description.abstractCancer is one of the age-related diseases with detrimental impact on people survival. Improvement of cancer therapies is a major focus of many scientists around the world. Anticancer drugs based on the microtubules inhibition are successfully used to treat widerange of cancers. Anti-microtubules drugs directly bind to colchicine, vinca and taxol binding sites on beta-tubulin, resulting in the impairment of spindle formation, vesicle transport, cell structure and migration. One of the modes of action anti-tubulin drugs is through causing faults in mitotic spindle function, which lead to the prolonged mitotic block and consequently to cell death. Although, drugs' high toxicity and development of resistance in patients lead to the idea of revisiting the dosage and combination therapies of anti-tubulin drugs, some sources reported that cell migration is more sensitive to microtubule inhibiting drugs than to cell proliferation in endothelial cells. Previously, we reported observations on NIH/3T3 (normal fibroblasts) cell proliferative activity, cell migration and direct test of microtubule dynamics. Thus, we aimed to identify effect of microtubule inhibitors on cancer cell lines. In addition, we compare normal cell lines with human cancer cell lines such as A549 (lung carcinoma), HT1080 (fibrosarcoma) and U118 (glioma).ru_RU
dc.identifier.citationBalabiyev A., Kakpenova A., Kauanova S., and Vorobjev I.A. 2016. Cancer cells response on the microtubuler-inhibiting drugs. Abstract book. 4 th International Scientific Conference “Regenerative medicine & healthy aging”. National Laboratory Astana, Nazarbayev University. http://nur.nu.edu.kz/handle/123456789/1512ru_RU
dc.identifier.urihttp://nur.nu.edu.kz/handle/123456789/1512
dc.language.isoenru_RU
dc.rightsAttribution-NonCommercial-ShareAlike 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/us/*
dc.subjectCancerru_RU
dc.subjectcancer therapiesru_RU
dc.subjectAnticancer drugsru_RU
dc.subjectmicrotubules inhibiting drugsru_RU
dc.titleCancer cells response on the microtubuler-inhibiting drugsru_RU
dc.typeAbstractru_RU

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