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1.

Glushchenko N. M. 
Risk assessment of cancer of the female reproductive system [Електронний ресурс] / N. M. Glushchenko, I. P. Nesina, N. P. Iurchenko, L. A. Proskurnya, L. G. Buchynska // Experimental oncology. - 2014. - Vol. 36, № 3. - С. 207-211. - Режим доступу: http://nbuv.gov.ua/UJRN/EOL_2014_36_3_13
Aim - to create an information resource concerning multifactorial oncological diseases of (he female reproductive system. A comprehensive search of the literature in the PubMcd and Ukrainian scientific sources published from 1995 to 2014 and the results of researches performed in R. E. Kavetsky Institute of Experimental Pathology, Oncology and Radiobiology, National Academy of Sciences of Ukraine. Development environment of information resource "Multifactorial oncological disease" was Borland Delphi. The information content of web page concerning cancers of the female reproductive system was posted in the information resource "Multifactorial oncological disease". The assessment algorithm of genetic contribution to cancers of the female reproductive system and recurrent risk of cancer development in families have been described. These algorithms can be used in assessment of contribution of genetic and environmental factors in the development of malignant tumors.
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2.

Iurchenko N. P. 
Comprehensive analysis of intratumoral lymphocytes and FOXP3 expression in tumor cells of endometrial cancer [Електронний ресурс] / N. P. Iurchenko, N. M. Glushchenko, L. G. Buchynska // Experimental oncology. - 2014. - Vol. 36, № 4. - С. 262-266. - Режим доступу: http://nbuv.gov.ua/UJRN/EOL_2014_36_4_11
Aim - to study the tumor microenvironment (CD4+, CD8+ and FOXP3+ lymphocytes) and FOXP3 expression by tumor cells and correlation of studied parameters with clinical and morphological characteristics of endometrial adenocarcinomas. Tumor samples from 40 patients (mean age 56,9 +- 2,8) with endometrial cancer (EC), who did not receive special treatment before surgery (chemotherapy, radiation therapy and hormontherapy), were investigated. Morphological, immunohis-tochemical methods as well as methods of mathematical statistics were applied in the study. It has been determined that high quantity of FOXP3+ tumor cells and intratumoral CD4+ and CD8+ T-Iymphocytes along with the low content of FOXP3+-lymphocytes is typical for the endometrial adenocarcinomas of high differentiation grade (G1). In poorly differentiated (G3) EC an increase of number of FOXP3+-lymphocytes and decrease of CD4+ and CD8+ lymphocytes in lymphocytic infiltrate have been observed. Moreover, decrease of the content of FOXP3+ tumor ceils has been determined. In EC patients correlation between the following parameters has been detected: proliferative activity and deep invasion of tumor in myometrium (R = 0,74); depth of invasion correlated with the number of the FOXP3+ tumor cells (R = -0,63) and number of CD4+ and CD8+ lymphocytes (R = 0,68 and R = -0,55 respectively) in lymphocytic infiltrate. Thus, results of this study are the evidence of significance of the lymphocytic components of tumor microenvironment and content of FOXP3 expressing tumor cells in EC progression. Conclusion: quantitative changes of tumor microenvironment, such as number of CD4+, CD8+ and FOXP3+ lymphocytes and content of FOXP3+ tumor cells correlate with biological characteristics of EC.
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