Georgian Scientists/ . 6 N 2, 2024 178 Georgian Scientists Vol. 6 Issue 2, 2024 https://doi.org/10.52340/gs.2024.06.02.17 1; 2; 3; 4; 5 1 Phd ; Email: teonaturashvili87@yahoo.com; 2 ; , Emai: g.tevdorashvili@tsmu.edu;3 ; E-mail: niniatevzadze1@gmail.com; 4 Phd ; ; E-mail: shota.kepuladze@gmail.com; https://orcid.org/0000-0002-5919-5581; 5 , ; E-mail: burkadze@yahoo.com; g.burkadze@tsmu.edu https://orcid.org/0000-0002-5028-4537 , . . , , . , , . , . , . . , - . Georgian Scientists/ . 6 N 2, 2024 179 , (FFPE) 315 . E- , , , , . Beta-catenin- , . , . P53- , , P53- . : ; ; EMT ; ; , . . , .1,2 , . . .3 , , , , . , , , . , , . , Georgian Scientists/ . 6 N 2, 2024 180 , , .4 , , . p53 . , , . , , . , . ( ), . , , . , . p53- . 5 , , p53- , . . , Ki67- , ( ) .6,7 . , , 5%- , Ki67 . . , . Georgian Scientists/ . 6 N 2, 2024 181 . , .8 , , . 5 80%- ), . 9 . , . , . , Wnt- . Axin-2, Wnt , .10 Axin-2- in vivo in vitro . Axin-2 p . , Axin-2 , .10 , Musashi-1- ( ) . in vitro , Musashi-1- .11 in vivo Musashi-1- , 40%- .11 . , . , , , , . Georgian Scientists/ . 6 N 2, 2024 182 , , , , . . . , . , , , . , . , , . , , , . , , , . , , , , . , .12– 14 , . , . , , , , , , . , . . , , , Georgian Scientists/ . 6 N 2, 2024 183 , . 12,15 . , E- . , , . , E- . , , , , 15. , . , E- , . E- , E- . , . , Wnt/ - .16 , , E - . , E - . 17,18 . , E- . , 2019-2023 . , (FFPE) 315 . 45 - ; 45 - ; 45 - ; Georgian Scientists/ . 6 N 2, 2024 184 45 - ; 45 - ; 45 - 45 - (H&E) , QuPath- . . . NovolinkTM Max Polymer Detection System. H&E ( ; .). : Spearman rank test- Mann-Whitney Kruskal-Wallis . 95%- . P <0.05 . SPSS statistical software V29.0- . E-cadherin- , (16,4±0,7) (14,8±1,0), (14,8±1,0). Beta-catenin- (21,4±1,2), (41,4±1,3), (16,4±0,9). Vimentin- (36,7±1,2), (41,5±0,9). E-cadherin- , (18,4±1,2). , (18,1±1,2). Beta-catenin- (26,5±0,8), (36,4±1,3). , (18,2±1,3). Vimentin- (24,8±1,2). Georgian Scientists/ . 6 N 2, 2024 185 , (36,8±1,4). 1. A. E-cadherin- , IHC, X100; B. E- cadherin- , IHC, X200; C. Beta-catenin- , IHC, X200; D. Beta-catenin- , IHC, X200; E. , IHC, X200; F. , IHC, X200; E-cadherin (21,4±1,6). (13,4±0,8). Beta-catenin- (9,8±1,1), (56,7±1,5). Beta-catenin- (9,7±0,2). Vimentin- (19,4±1,5) (17,3±1,0), (60,4±1,6). Vimentin- (28,7±0,6). Georgian Scientists/ . 6 N 2, 2024 186 E-cadherin Beta- catenin Vimentin 16,4±0,7 21,4±1,2 30,5±1,3 14,1±1,3 18,9±0,6 26,7±0,9 21,8±1,0 28,3±0,5 34,4±1,3 21±1,0 32,8±0,6 44,3±1,1 14,8±1,0 41,4±1,3 36,7±1,2 28,1±0,9 16,4±0,9 41,5±0,9 12,5±0,2 30,5±1,2 16,7±1,1 8,5±0,3 25,3±0,5 18,4±1,2 16.0±0,8 26,5±0,8 20,5±1,0 18,4±1,2 36,4±1,3 24,8±1,2 0 0 0 18,1±1,2 18,2±1,3 36,8±1,4 35,4±0,6 12,3±6,9 19,4±1,5 43,2±0,7 9,8±1,1 17,3±1,0 32,5±1,0 11,7±0,6 44,5±1,6 28,3±1,6 38,4±0,4 42,7±0,2 21,4±1,6 56,7±1,5 60,4±1,6 13,4±0,8 9,7±0,2 28,7±0,6 1. E-cadherin- , Beta-catenin- Vimentin- Georgian Scientists/ . 6 N 2, 2024 187 P53- ) , P53- 15,3±0,7. CD44 (44,1±0,9), (36,4±1,5) (42,5±2,1). P53 , (12,4±0,8), (15,6±1,7). . P53 (15,7±1,2). CD44 (34,5±1,2), , (48,3±1,8). 2. A. CD44- , IHC, X200; B. CD44- , IHC, X200; C. P53- , IHC, X200; D. P53- , IHC, X200. Georgian Scientists/ . 6 N 2, 2024 188 P53 . (16,1±0,4) (10,3±1,1). (62,8±2,2). CD44- (42,2±0,7), (32,4±1,7), (56,2±1,8) (62,7±1,7). P53 CD44 neg 38,7±1,3 neg 44,9±1,1 neg 43,1±1,1 neg 44,1±0,9 15,3±0,7 36,4±1,5 neg 42,5±2,1 neg 32,7±1,1 neg 36,2±0,7 12,4±0,8 34,2±1,5 15,6±1,7 34,5±1,2 0 0 15,7±1,2 48,3±1,8 neg 42,2±0,7 neg 32,5±0,9 neg 26,4±0,4 16,1±0,4 32,4±1,7 10,3±1,1 56,2±1,8 62,8±2,2 62,7±1,7 2. P53- CD44- Georgian Scientists/ . 6 N 2, 2024 189 E-cadherin- 19- , 22,9- . 29,1- , 34,7- , . 10,7- , 16,5- . 7,3- , 9,9- , . , 6,6- . E-cadherin- 14,7- , 4,7- , . Beta-catenin- 9,1- , 18,2- . 9,1- , 15,5- , . 16,6- , 14,8- . , 5.6- , 2- . 15,3- , . 6,7- , 8,5- . 11,1- , 2,7- , . Georgian Scientists/ . 6 N 2, 2024 190 9,4- , 1,1- . 10,1- , 24,- . 1,7- , 20,9- , . 23,7- . , 12,8- , 8,1- . 1. E-cadherin- , Beta-catenin- Vimentin- CD44- 3,5- , 9,5- . 12,4- , 3,7- , . 14,9- Georgian Scientists/ . 6 N 2, 2024 191 7,8- . 11,7- , 2,1- , . 19,8- . , 20,2- , 14,4- CD44- . P53- . . , , 0,5- . P53- 5- . . , , P53- 47,1- . Georgian Scientists/ . 6 N 2, 2024 192 2. P53- CD44- E- , , , , . , E- . Beta-catenin- , . , Beta- . , , . . , . Georgian Scientists/ . 6 N 2, 2024 193 CD44- , . P53- , , , . P53- , , P53- . : 1.D’Angelo, E. et al. Atypical Endometrial Hyperplasia, Low-grade: ‘much ADO about Nothing’. American Journal of Surgical Pathology 45, 988–996 (2021). 2. Lax, S. F. [Precursor lesions of endometrial carcinoma]. Pathologe 40, 13–20 (2019). 3. Stringfellow, H. F. & Elliot, V. J. Endometrial metaplasia. Diagn Histopathol 23, 303–310 (2017). 4.Travaglino, A. et al. 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Features of epithelial-mesenchymal transformation and distribution of stem cells during Endometrial ciliary/tubal metaplasia Teona Turashvili1; George Tevdorashvili2; Nino Tevzadze3; Shota Kepuladze4; George Burkadze5 1MD, Phd Student at Tbilisi State medical University; 2Professor at Tbilisi State Medical University, Gynecology and Obstetrics; 3Resident in Clinical Pathology at Tbilisi State medical University; 4Phd Student at Tbilisi State medical University; AP/CP pathologist; MD; 5Professor at Tbilisi State Medical University, Head of the Department of Molecular pathology; Abstract Metaplasia is an adaptive process in which one tissue is transformed into another tissue that is functionally and morphologically different. The most common type of metaplasia in the endometrium is ciliary/tubal metaplasia. Although the immunophenotype of ciliary/tubal metaplasia in the cervix is well studied, there are very few studies related to endometrial metaplasia. There is no reliable clinical evidence that tubal metaplasia is a precursor to serous carcinoma. It is highly likely that the precursor may be a highly differentiated endometrioid carcinoma with extensive ciliary changes. In the progression of endometrial pathologies, the role of epithelial-mesenchymal transformation is not completely clear. Epithelial-mesenchymal transformation is also a probable cause of endometrioid-type carcinomas. Within the framework of our research, a cohort retrograde study was carried out, for which archival material of the teaching-scientific and diagnostic laboratory of Tbilisi State Medical University was used. Overall, the study included a total of 315 non-fixed formalin-fixed and paraffin-embedded (FFPE) cases. Our study showed that the expression analysis of E-cadherin showed that its expression was significantly decreased in the study groups, in contrast to the study groups without metaplasia, indicating the independent behavior and importance of ciliary as well as atypical ciliary metaplasia in endometrial carcinogenesis. Beta-catenin expression in ciliary metaplasia, as well as in atypical ciliary metaplasia, increases progressively with the development of atypical processes in the endometrium. Accordingly, vimentin can be used as an independent molecular marker for monitoring tubal metaplasia. A lower significance of P53-dependent carcinogenesis was observed in endometrial neoplastic processes, in contrast to serous carcinoma, where P53 expression is significantly higher. Key words: endometrial metaplasia; Ciliary metaplasia; EMT transformation; stem cells;