DETERMINATION OF EXPRESSION RATE OF MOLECULAR BIOLOGICAL MARKERS IN TUMOR OF PATIENTS WITH STAGE I-IV ENDOMETRIAL CANCER TO PREDICT THE DISEASE RELAPSE

2020 ◽  
pp. 54-58
Author(s):  
Marina Anatolevna Teplova ◽  
Irina Nikolaevna Krugova ◽  
Yuliia Anatolevna Moiseyenko ◽  
Natalia Nikolaevna Shchyt

In order to study the molecular biological markers of the tumor in patients with endometrial cancer stages I−IV, the patients who received a combined treatment at the Department of Oncological Gynecology at the State Institution "Grigoriev Institute for Medical Radiology" were surveyed. The study has demonstrated that in the patients with advanced endometrial cancer, the expression rate of molecular biological markers and ER and PR receptors depends on the histological shape of the tumor. In adenocarcinomas with a high degree of differentiation, the value of both positive and negative VEGF was observed in equal percentages, against the background of high Bcl−2 expression, negative mt p53 expression, and negative or moderate proliferative activity. In patients with adenocarcinoma with moderate degree of differentiation, the value of positive VEGF was observed three times more often than negative one, against the background of a high Bcl−2 expression, negative mt p53 expression and moderate proliferative activity (Ki67). In the patients with low−grade adenocarcinoma endometrium, both positive and negative VEGF were equal in percentage, against the background of high Bcl−2 expression, negative mt p53 expression, and positive proliferative activity. In adenocarcinomas with high and moderate degree of differentiation, the positive status of ER and PR is more often observed, and, conversely, in the patients with low−differentiated adenocarcinoma their negative status was found. It has been revealed that the level of expression of the investigated molecular biological markers and ER and PR receptors in tumors of the patients with endometrial cancer differed depending on the occurrence of relapse. This fact can be used to determine the risk of endometrial cancer recurrence. Key words: endometrial cancer, molecular biological markers, relapse, expression.

2002 ◽  
Vol 12 (1) ◽  
pp. 110-118 ◽  
Author(s):  
C Lundgren ◽  
G Auer ◽  
B Frankendal ◽  
B Moberger ◽  
B Nilsson ◽  
...  

Abstract.Lundgren C, Auer G, Frankendal B, Moberger B, Nilsson B, Nordström B. Nuclear DNA content, proliferative activity, and p53 expression related to clinical and histopathologic features in endometrial carcinoma.The purpose of this study was to evaluate the prognostic impact of image cytometry DNA ploidy, MIB-1, and p53 in relation to clinicopathologic variables in 376 consecutive patients with endometrial carcinoma stages I–IV. Following primary treatment 358 patients were considered tumor-free. Relapses and tumor-specific deaths of these patients were noted. Image cytometry DNA ploidy (n = 340) and expression of MIB-1 (n = 318) and p53 (n = 323) were studied. In univariate analysis, stage (P < 0.001), histopathologic subtype (P < 0.001), degree of differentiation (P < 0.001), HRT (P = 0.034), DNA ploidy (P < 0.001), and p53 (P < 0.001) were significant predictors of relapse. Patient age showed that the estimated mean risk of relapse increases with nearly 64% per decade in life (P 0.003), and the MIB-1 expression with 21% per 10-unit increment (P 0.004). In multivariate analysis, degree of differentiation, MIB-1, and p53 lost their prognostic capability. However, after stage and histopathologic subtype, image cytometry DNA ploidy was the strongest predictor of outcome and was of value in predicting the risk for relapse. The combination of DNA ploidy, MIB-1, and p53 expression was an even stronger predictor of relapse-free survival than the individual prognostic factors.


2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Xiao Li ◽  
Yiping Gao ◽  
Mingzi Tan ◽  
Huiyu Zhuang ◽  
Jian Gao ◽  
...  

The main aims of this study were to determine the expression of human epididymis protein 4 (HE4) in endometrial cancer and to explore the relationships between HE4 expression, clinicopathological parameters, and prognosis. Immunohistochemistry was used to detect HE4 expression in 102 cases of endometrial cancer, 30 cases of endometrial atypical hyperplasia, and 20 cases of normal endometrium. The positive expression rate of HE4 in endometrial carcinoma was 84.62%, significantly higher than 66.67% in atypical hyperplasia (P<0.05) and 15.00% in normal endometrium (P<0.0.01). With the exception of stage II, HE4 expression in endometrial cancer showed an increasing tendency with increased clinical stage (P<0.05). The positive expression rate of HE4 increased with a decrease in the degree of differentiation. A statistically significant difference was observed between the highly differentiated group and the poorly differentiated group (P<0.05). Mortality in endometrial cancer patients with high HE4 expression was significantly higher than that in patients with low HE4 expression (P<0.05). Endometrial cancer patients with high HE4 expression have a poor prognosis.


2015 ◽  
Vol 33 (15_suppl) ◽  
pp. e16510-e16510
Author(s):  
Woojin Chong ◽  
Bryan Harmon ◽  
Anne R. Van Arsdale ◽  
Nicole Nevadunsky ◽  
Kathleen Whitney ◽  
...  

2003 ◽  
Vol 111 (06) ◽  
Author(s):  
C Tanase ◽  
E Codorean ◽  
C Ardeleanu ◽  
D Terzea ◽  
G Butur ◽  
...  

Author(s):  
Koji Matsuo ◽  
Rachel S. Mandelbaum ◽  
Shinya Matsuzaki ◽  
Maximilian Klar ◽  
Lynda D. Roman ◽  
...  

1993 ◽  
Vol 3 (6) ◽  
pp. 363-368 ◽  
Author(s):  
T. Hachisuga ◽  
K. Fukuda ◽  
M. Uchiyama ◽  
N. Matsuo ◽  
T. Iwasaka ◽  
...  

Using anti-p53 (PAb1801 and PAb240), anti-DNA polymerase α and Ki-67 monoclonal antibodies, the expression of p53 was studied in 11 normal endometria, 14 endometrial hyperplasias and 27 endometrial carcinomas and its relationship to the proliferative activity of the tumors was examined. Normal endometria and simple hyperplasias were completely negative for p53. The PAb1801 indices of complex hyperplasias and complex atypical hyperplasias were 2.5±1.8% and 5.0±3.2%, respectively. The PAb1801 indices of grade 1, grade 2 and grade 3 endometrial carcinomas were 10.2±14.2%, 44.4±29/0% and 45.0±32.5%, respectively. These results indicate a progressively enhanced p53 expression in the sequence from normal endometrium, through hyperplasia to carcinoma. A significant correlation between p53 expression and labeling indices of Ki-67 and DNA polymerase α was observed in endometrial carcinomas. The endo-metrial carcinomas with p53 overexpression developed mainly in post-menopausal patients and were frequently high-grade tumors with deep myometrial invasion. These findings may indicate that overexpression of p53 protein contributes to the proliferative activity of the tumor cells.


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