Xin yixue (Mar 2023)

Expression levels of TTF-1 and CyclinD1 and their relationship with lymphangiogenesis in ovarian cancer

  • Zhang Xin, Yan Qianwen, Wang Luyi

DOI
https://doi.org/10.3969/j.issn.0253-9802.2023.03.006
Journal volume & issue
Vol. 54, no. 3
pp. 191 – 196

Abstract

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Objective To investigate the expression levels of thyroid transcription factor-1 （TTF-1） and CyclinD1 in ovarian cancer and analyze their relationship with lymphangiogenesis. Methods The ovarian cancer tissue samples were collected from 60 patients with ovarian cancer and corresponding ovarian tissue samples from 20 patients pathologically diagnosed with benign ovarian tumors and normal ovarian tissue were collected as the control group. Tissue sections were prepared for immunohistochemical staining of TTF-1， CyclinD1 and D2-40. The staining results of TTF-1 and CyclinD1 were evaluated based on semi-quantitative integration method. D2-40 staining results were assessed according to Weidner evaluation method. Lymphatic vessel density （LVD） was calculated. Results The positive expression rates of TTF-1 and CyclinD1 were 58% and 83% in the ovarian cancer tissues， which were higher than 5% and 10% in the normal cancer tissues（all P < 0.001）， respectively. The positive expression rates of TTF-1 and CyclinD1 were significantly increased in the ovarian cancer tissues with pathological stageⅢ-Ⅳ， lymph node metastasis， peritoneal metastasis， T3-T4 stage， N1 stage and M1 stage （all P < 0.05）. Age and histological type were not correlated with the positive expression rates of TTF-1 and CyclinD1 （all P > 0.05）. The LVD of ovarian cancer tissues with pathological stageⅢ-Ⅳ， lymph node metastasis and peritoneal metastasis was significantly increased （all P < 0.05）. The LVD of ovarian cancer tissues with positive expression of TTF-1 and CyclinD1 was significantly higher than that of ovarian cancer tissues with negative expression （both P < 0.05）. Conclusions TTF-1 and CyclinD1 are highly expressed in ovarian cancer tissues. Patients with severe ovarian cancer， lymphangiogenesis and metastasis have high expression of TTF-1 and CyclinD1， which may be potential new targets for ovarian cancer interventions.

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