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<title>Experimental Oncology, 2016 (том 38)</title>
<link href="http://dspace.nbuv.gov.ua:80/handle/123456789/133168" rel="alternate"/>
<subtitle/>
<id>http://dspace.nbuv.gov.ua:80/handle/123456789/133168</id>
<updated>2026-04-06T23:08:13Z</updated>
<dc:date>2026-04-06T23:08:13Z</dc:date>
<entry>
<title>Inhibition of malignant potential and expression of proteins associated with epithelial-mesenchymal transition in Lewis lung carcinoma cells transduced with murine ifn-β gene in recombinant baculovirus</title>
<link href="http://dspace.nbuv.gov.ua:80/handle/123456789/140132" rel="alternate"/>
<author>
<name>Lykhova, O.</name>
</author>
<author>
<name>Kovalova, O.</name>
</author>
<author>
<name>Bezdenezhnykh, N.</name>
</author>
<author>
<name>Adamenko, I.</name>
</author>
<author>
<name>Vorontsova, A.</name>
</author>
<author>
<name>Strokovska, L.</name>
</author>
<author>
<name>Kudryavets, Yu.</name>
</author>
<id>http://dspace.nbuv.gov.ua:80/handle/123456789/140132</id>
<updated>2018-06-23T00:03:13Z</updated>
<published>2016-01-01T00:00:00Z</published>
<summary type="text">Inhibition of malignant potential and expression of proteins associated with epithelial-mesenchymal transition in Lewis lung carcinoma cells transduced with murine ifn-β gene in recombinant baculovirus
Lykhova, O.; Kovalova, O.; Bezdenezhnykh, N.; Adamenko, I.; Vorontsova, A.; Strokovska, L.; Kudryavets, Yu.
Aim: To analyze biological characteristics. malignant potential and expression of proteins associated with epithelial mesenchynal&#13;
transition in murine lung carclnoma cells transduced with intertcron-beta (ifn-β) gene in baculovirus vector. Materials and Methods: The study was perforated on Lewis lung carcinoma (LL) cells transduced with ifn-β gene in recombinant baculovirus vector.&#13;
Biological characterlstics of the LL cells were studied with the use of standard cell culture method, cytogenetic and immunocytochemical assays. Resutes: Recombinant baculmirus-mediated transduction of LL cells with ifn-β gene resulted in siguﬁcant decrease&#13;
of cell growth rate and density both in complete and serum-foee medium. Also. LL cells transduction with ifn-β gene signiﬁcantly&#13;
inhﬂtited cell migration in vitro. Transduction of LL cells by baculovirus vector with or withoot ifn-β  gene caused signiﬁcant genotoxic effect in these cells. Furthermore. ifn-β gene transfer to lung carcinoma cells resulted in signiﬁcant increase of nuclear expression of p19ARE (p &lt; 0.01). p21WAFI (p &lt; 0.001). cytoplasmic expression of E-cadherin (p &lt; 0.005) and inhibition of transcription&#13;
factors of epithelial-mesenchymal transition (EMT) Tmist (p &lt; 0.005) and Slug (p &lt; 0.00 I) expression. Conclusions; Transduction&#13;
with ifn-β gene of LL cells in recombinant baculovirus resulted in aquirement of less malignant phenotype in vitro and suppressed&#13;
expression ofproteins associated with EMT.
</summary>
<dc:date>2016-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>miR-608 rs4919510 C&gt;G polymorphism decreased the risk of breast cancer in an Iranian subpopulation</title>
<link href="http://dspace.nbuv.gov.ua:80/handle/123456789/140089" rel="alternate"/>
<author>
<name>Hashemi, M.</name>
</author>
<author>
<name>Sanaei, S.</name>
</author>
<author>
<name>Rezaei, M.</name>
</author>
<author>
<name>Bahari, G.</name>
</author>
<author>
<name>Hashemi, S.M.</name>
</author>
<author>
<name>Mashhadi, M.A.</name>
</author>
<author>
<name>Taheri, M.</name>
</author>
<author>
<name>Ghavami, S.</name>
</author>
<id>http://dspace.nbuv.gov.ua:80/handle/123456789/140089</id>
<updated>2018-06-23T00:03:13Z</updated>
<published>2016-01-01T00:00:00Z</published>
<summary type="text">miR-608 rs4919510 C&gt;G polymorphism decreased the risk of breast cancer in an Iranian subpopulation
Hashemi, M.; Sanaei, S.; Rezaei, M.; Bahari, G.; Hashemi, S.M.; Mashhadi, M.A.; Taheri, M.; Ghavami, S.
Aim: MicroRNAs (miRNAs) are small noncoding RNAs that function as oncogene or tumor suppressors. The single nucleotide&#13;
polymorphisms in miRNAs potentially can alter miRNA-binding sites on target genes as well as affecting miRNAs expression. The&#13;
present study aimed to evaluate the impact of miR-608 rs4919510 C&gt;G variant on breast cancer (BC) risk. Materials and Methods:&#13;
This case-control study conducted on 160 women with BC and 192 age-matched healthy women. Genotyping of miR608&#13;
rs4919510 was done using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Results:&#13;
Our findings showed that GC genotype significantly decreased the risk of BC (odds ratio (OR) = 0.49, 95% confidence interval&#13;
(CI) 0.28–0.88, p = 0.018) compared to CC genotype. Furthermore the G allele decreased the risk of BC (OR = 0.53,&#13;
95%CI 0.30–0.92, p = 0.024). No significant association was found between miR-609 genotypes and clinicopathological characteristics&#13;
of BC patients (p &gt; 0.05). Conclusion: Our findings indicate that miR-608 polymorphism might be associated with decreased&#13;
risk of BC in an Iranian subpopulation. Further large-scale studies with different ethnicities are needed to verify our findings.
</summary>
<dc:date>2016-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>The III Swedish-Ukrainian meeting on cancer diseases</title>
<link href="http://dspace.nbuv.gov.ua:80/handle/123456789/140056" rel="alternate"/>
<author>
<name/>
</author>
<id>http://dspace.nbuv.gov.ua:80/handle/123456789/140056</id>
<updated>2018-06-23T00:03:03Z</updated>
<published>2016-01-01T00:00:00Z</published>
<summary type="text">The III Swedish-Ukrainian meeting on cancer diseases
</summary>
<dc:date>2016-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Radioprotective properties of sodium humate in radiation-induced mutagenesis in cultured lymphocytes of thyroid cancer patients</title>
<link href="http://dspace.nbuv.gov.ua:80/handle/123456789/138003" rel="alternate"/>
<author>
<name>Shkarupa, V.M.</name>
</author>
<author>
<name>Klymenko, S.V.</name>
</author>
<id>http://dspace.nbuv.gov.ua:80/handle/123456789/138003</id>
<updated>2018-06-18T00:05:20Z</updated>
<published>2016-01-01T00:00:00Z</published>
<summary type="text">Radioprotective properties of sodium humate in radiation-induced mutagenesis in cultured lymphocytes of thyroid cancer patients
Shkarupa, V.M.; Klymenko, S.V.
Aim: To investigate the effect of sodium humate on the level of cytogenetic damage in culture of lymphocytes of patients with thyroid cancer after γ-irradiation. Materials and Methods: Metaphase analysis of chromosome aberrations in cultured peripheral blood lymphocytes of 10 individuals with thyroid cancer was performed after irradiation of lymphocytes in vitro at a dose of 1 Gy from ¹³⁷Cs source at the early G₀ phase of cell cycle. Sodium humate was added to cell culture for 30 ± 15 min after phytohemagglutinin stimulation at concentrations of 10 and 100 μg/ml. Results: Sodium humate exhibited antimutagenic properties. The preparation at a concentration of 10 μg/ml was more effective than at a concentration of 100 μg/ml, reducing the average incidence of radiation-induced chromosome aberrations by 51.88 and 38.77%, respectively. The most pronounced antimutagenic effect of sodium humate was the reduction of the frequency of chromosomal type aberrations, however, such efficiency varied between individual patients with thyroid cancer. Conclusions: Sodium humate could be considered as a potential therapeutic modifier of radiation damage.
</summary>
<dc:date>2016-01-01T00:00:00Z</dc:date>
</entry>
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