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A functional approach for searching biomarkers of glioma
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Cancer Science & Therapy

ISSN: 1948-5956

Open Access

A functional approach for searching biomarkers of glioma


Cancer Diagnostics Conference & Expo

June 13-15, 2016 Rome, Italy

Kopylov A, Pasynkova K, Pustogarov N, Revishchin A and Pavlova G

Lomonosov Moscow State University, Russia
Institute of Gene Biology-RAS, Russia
Apto-Pharm Ltd, Russia

Posters & Accepted Abstracts: J Cancer Sci Ther

Abstract :

Trends in developing biomarker for tumors, including gliomas are bifurcated into following directions. Firstly, studying differential expression of genes in tumors versus corresponding normal tissues is done. Secondly, expert studying of expression of particular genes selected according to presumed function in glioblastoma multiform (GBM) development and malignancy. Neural cancer stem cells (CSCs) or neural/glial cancer progenitor cells (CPCs) are developing into different glioma grades: Diffuse astrocytoma (II), anaplastic astrocytoma (III), primary and secondary glioblastomas (IV). Series of surgical specimens with different clinical cases were analyzed by RT-qPCR. GBM is built by hierarchies developed by tumorigenic GSCs, which are controlled by Notch, Wnt, BMP, TGFb, RTK pathways. We have studied expression of some of these genes in progression of astrocytomas and GBM; in particular, growth factor receptors EGFR, PDGFR, FGFR, Notch; members of signaling pathways, including cytoplasmic and nuclear intermediates (MELK, MAP, TUBB3, GFAP and CDK4, CDK6, MDM2,GAPDH); and transcription factors (OLIG2, SOX2, OCT4, NANOG). Some marker of SCs and neural differentiation were also included (CD133). The level of expression of EGFR was increased in the majority of GBM compared to other grades. The rate of expression of PDGFR was fairly similar; though PDGFR expression level was lower. Both genes could be developed to diagnostic markers. Expression level of transcription factors (sox2, oct4, nanog) involved in maintenance of stemness was increased in all samples, suggesting relationship between stemness and GBM progression.

Biography :

Kopylov A has completed his PhD from Chemistry Department, Lomonosov Moscow State University and Doctor of Chemistry from the same University. He was Post-Doc at University of California Santa Cruz and Invited Professor at University of Massachusetts, USA. He is the Lecturer and the Group Leader at the University and Science Director of Apto-Pharm start-up. He has published about 70 papers in reputed journals.

Email: kopylov.alex@gmail.com

Google Scholar citation report
Citations: 3968

Cancer Science & Therapy received 3968 citations as per Google Scholar report

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