Nataša Tošić
Naučni savetnik
Laboratorija za molekularnu biomedicinu
GRUPA ZA MOLEKULARNU BIOMEDICINU
Institut za molekularnu genetiku i genetičko inženjerstvo (IMGGI),
Univerzitet u Beogradu,
Vojvode Stepe 444a, 11042 Beograd 152, Srbija
Mob: +381 65 397 64 45
Tel: +381 11 397 64 45
Fax: +381 11 397 58 08
E-mail: natasa.tosic@imgge.bg.ac.rs
OBRAZOVANJE
2010 - Doktor bioloških nauka, Biološki fakultet (BF), Univerzitet u Beogradu (UB),
(Interakcija genetičkih markera proliferacije, diferncijacije i apoptoze kod akutnih leukemija)
2002 - Magistar bioloških nauka, BF, UB
1998 - Diplomirani molekularni biolog i fiziolog, BF, UB
ISTRAŽIVAČKO ISKUSTVO
2021 - naučni savetnik, IMGGI, UB
2016 – 2021 viši naučni saradnik, IMGGI, UB
2011 - 2016 - naučni saradnik, IMGGI, UB
2003 - 2011 - istraživač saradnik, IMGGI, UB
1999 - 2000 - istraživač pripravnik, Institut Vinča, Beograd
OSTALE AKTIVNOSTI
2012-2021 - predavač na doktorskim studijama na Biološkom fakultetu, UB, u okviru studijskog programa molekularna biologija (predmeti „Molekularna genetika bolesti čoveka“, „Molekularna hematologija“ i „Personalizovana medicina i farmakogenetika“)
2019 - član Naučnog veća IMGGI, UB
2013 – 2016 - Strengthening the Research Potential of IMGGE through Reinforcement of Biomedical Science of Rare Diseases in Serbia – en route for innovation, SERBORDISinn (EU-FP7-REGPOT, 316088, 2013-2016), rukovodilac WP2c
2011 – 2019 - „Retke bolesti: molekularna patofiziologija, dijagnostički i terapijski modaliteti i socijalni, etički i pravni aspekti“ (MPNTR, III 41004, 2011-2019), rukovodilac projektnih zadataka u okviru potprojekata 3 i 4: „Dijagnostički i prognostički molekularni markeri kod limfoproliferativnih oboljenja“ i „Molekularnogenetički i imunofenotipski markeri klonskog preobražaja matičnih ćelija hematopoeze“
OBLAST NAUČNOG INTERESOVANJA
Istraživanja u oblasti genetike kancera sa fokusom na hematološke malignitete. Detekcija genetičkih promena koji leže u osnovi procesa kancerogeneze. Molekularni markeri značajni za dijagnozu i terapiju kancera.
2017 – 2021 - Leukemia Gene Discovery by data sharing, mining and collaboration - LEGEND (CA16223) – (COST, 2017-2021), učesnik
2013 – 2016 - Strengthening the Research Potential of IMGGE through Reinforcement of Biomedical Science of Rare Diseases in Serbia – en route for innovation, SERBORDISinn (EU-FP7-REGPOT, 316088, 2013-2016), rukovodilac WP2c
2011 – 2019 - „Retke bolesti: molekularna patofiziologija, dijagnostički i terapijski modaliteti i socijalni, etički i pravni aspekti“ (MPNTR, III 41004, 2011-2019), rukovodilac projektnih zadataka u okviru potprojekata 3 i 4: „Dijagnostički i prognostički molekularni markeri kod limfoproliferativnih oboljenja“ i „Molekularnogenetički i imunofenotipski markeri klonskog preobražaja matičnih ćelija hematopoeze“
2006 – 2010 - Strukturalni elementi genoma u modulaciji fenotipa (MNTRS, 143051, 2006-2010), učesnik
2006 – 2009 - Health Improvement in Serbia through Reinforcement of Biomedical Science and Technology -HISERBS (EU FP6 SSA INCO-026357, 2006-2009), učesnik
2003 – 2005 - Mutirani gen u kontekstu drugih gena (MNZŽS, 1417, 2002-2005), učesnik
2000 - 2003 - volonter u Laboratoriji za imunologiju, Zavod za transfuziju Srbije, Beograd
1999 – 2000 - istraživač u Laboratoriji za antioksidativne enzime, Institut Vinča, Beograd
OSTALE AKTIVNOSTI
2012-2021 - predavač na doktorskim studijama na Biološkom fakultetu, UB, u okviru studijskog programa molekularna biologija (predmeti „Molekularna genetika bolesti čoveka“, „Molekularna hematologija“ i „Personalizovana medicina i farmakogenetika“)
2019 - član Naučnog veća IMGGI, UB
OBLAST NAUČNOG INTERESOVANJA
Istraživanja u oblasti genetike kancera sa fokusom na hematološke malignitete. Detekcija genetičkih promena koji leže u osnovi procesa kancerogeneze. Molekularni markeri značajni za dijagnozu i terapiju kancera.
ODABRANI NAUČNI RADOVI
Celokupna lista radova je dostupna na linku https://scholar.google.com/citations?user=k921DjoAAAAJ&hl=sr
Marjanovic I, Karan-Djurasevic T, Kostic T, Virijevic M, Vukovic NS, Pavlovic S, Tosic N. Prognostic significance of combined BAALC and MN1 gene expression level in acute myeloid leukemia with normal karyotype. Int J Lab Hematol. 2021 Jun;43(3):433-440. doi: 10.1111/ijlh.13405
Vesovic N, Tosic N, Karan Djurasevic T, Andric Z, Zdravkovic D, Pavlovic S, Jovanovic D. Expression pattern of circulating long non-coding RNA GAS5 as a novel biomarker in non-small cell lung cancer patients. Arch Med Sci. 2020 https://doi.org/10.5114/aoms.2020.98815
Mitrovic M, Kostic T, Virijevic M, Karan-Djurasevic T, Suvajdzic Vukovic N, Pavlovic S, Tosic N. The influence of Wilms' tumor 1 gene expression level on prognosis and risk stratification of acute promyelocytic leukemia patients. Int J Lab Hematol, 2020;42(1):82-87. doi: 10.1111/ijlh.13144
Tosic N, Petrovic I, Grujicic NK, Davidovic S, Virijevic M, Vukovic NS, Pavlovic S, Stevanovic M. Prognostic significance of SOX2, SOX3, SOX11, SOX14 and SOX18 gene expression in adult de novo acute myeloid leukemia. Leuk Res. 2018 Apr;67:32-38. doi:10.1016/j.leukres.2018.02.001
Todorovic Balint M, Jelicic J, Mihaljevic B, Kostic J, Stanic B, Balint B, Pejanovic N, Lucic B, Tosic N, Marjanovic I, Stojiljkovic M, Karan-Djurasevic T, Perisic O, Rakocevic G, Popovic M, Raicevic S, Bila J, Antic D, Andjelic B, Pavlovic S. Gene Mutation Profiles in Primary Diffuse Large B Cell Lymphoma of Central Nervous System: Next Generation Sequencing Analyses. Int J Mol Sci. 2016 May 6;17(5):683. doi: 10.3390/ijms17050683
Marjanovic I, Kostic J, Stanic B, Pejanovic N, Lucic B, Karan-Djurasevic T, Janic D, Dokmanovic L, Jankovic S, Vukovic NS, Tomin D, Perisic O, Rakocevic G, Popovic M, Pavlovic S, Tosic N. Parallel targeted next generation sequencing of childhood and adult acute myeloid leukemia patients reveals uniform genomic profile of the disease. Tumour Biol. 2016 Oct;37(10):13391-13401. doi: 10.1007/s13277-016-5142-7
Hackl H, Steinleitner K, Lind K, Hofer S, Tosic N, Pavlovic S, Suvajdzic N, Sill H, Wieser R. A gene expression profile associated with relapse of cytogenetically normal acute myeloid leukemia is enriched for leukemia stem cell genes. Leuk Lymphoma. 2015;56(4):1126-1128. doi: 10.3109/10428194.2014.944523
Puda A, Milosevic JD, Berg T, Klampfl T, Harutyunyan AS, Gisslinger B, Rumi E, Pietra D, Malcovati L, Elena C, Doubek M, Steurer M, Tosic N, Pavlovic S, Guglielmelli P, Pieri L, Vannucchi AM, Gisslinger H, Cazzola M, Kralovics R. Frequent deletions of JARID2 in leukemic transformation of chronic myeloid malignancies. Am J Hematol, 2012;87(3):245-250. doi: 10.1002/ajh.22257
Milosevic JD, Puda A, Malcovati L, Berg T, Hofbauer M, Stukalov A, Klampfl T, Harutyunyan AS, Gisslinger H, Gisslinger B, Burjanivova T, Rumi E, Pietra D, Elena C, Vannucchi AM, Doubek M, Dvorakova D, Robesova B, Wieser R, Koller E, Suvajdzic N, Tomin D, Tosic N, Colinge J, Racil Z, Steurer M, Pavlovic S, Cazzola M, Kralovics R. Clinical significance of genetic aberrations in secondary acute myeloid leukemia. Am J Hematol. 2012;87(11):1010-1016. doi: 10.1002/ajh.23309
Thomadaki H, Floros KV, Pavlovic S, Tosic N, Gourgiotis D, Colovic M, Scorilas A. Overexpression of the novel member of the BCL2 gene family, BCL2L12, is associated with the disease outcome in patients with acute myeloid leukemia. Clin Biochem. 2012;45(16-17):1362-1367. doi: 10.1016/j.clinbiochem.2012.06.012
Krstovski N, Tosic N, Janic D, Dokmanovic L, Kuzmanovic M, Spasovski V, Pavlovic S. Incidence of FLT3 and nucleophosmin gene mutations in childhood acute myeloid leukemia: Serbian experience and the review of the literature. Med Oncol. 2010 Sep;27(3):640-5. doi: 10.1007/s12032-009-9261-5
Lazić J, Tošić N, Dokmanović L, Krstovski N, Rodić P, Pavlović S, Janić D. Clinical features of the most common fusion genes in childhood acute lymphoblastic leukemia. Med Oncol. 2010;27(2):449-453. doi: 10.1007/s12032-009-9232-x
Tošić N, Stojiljković M, Čolović N, Čolović M, Pavlović S. Acute myeloid leukemia with NUP98-HOXC13 fusion and FLT3-ITD mutation: case report and review of the literature. Cancer Genet Cytogenet. 2009;193(2):98-103. doi: 10.1016/j.cancergencyto.2009.03.007
Čolović N, Tošić N, Aveić S, Djurić M, Milić N, Bumbaširević V, Čolović M, Pavlović S. Importance of early detection and follow-up of FLT3 mutations in patients with acute myeloid leukemia. Ann Hematol. 2007;86(10):741-7. doi: 10.1007/s00277-007-0325-3