Clinical Significance of Galectin-7 in Epithelial Ovarian Cancer

被引:0
作者
Kim, Ha-Jeong [1 ]
Jeon, Hye-Kyung [2 ]
Lee, Jae-Kwan [3 ]
Sung, Chang Ohk [4 ]
Do, In-Gu [5 ]
Choi, Chel Hun [2 ]
Kim, Tae-Joong [2 ]
Kim, Byoung-Gie [2 ]
Bae, Duk-Soo [2 ]
Lee, Jeong-Won [2 ]
机构
[1] Wonkwang Univ, Sanbon Hosp, Dept Obstet & Gynecol, Gunpo, South Korea
[2] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Obstet & Gynecol, Seoul 135710, South Korea
[3] Korea Univ, Coll Med, Dept Obstet & Gynaecol, Seoul 136705, South Korea
[4] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Pathol, Seoul, South Korea
[5] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Expt Pathol Ctr,Samsung Canc Res Inst, Seoul 135710, South Korea
关键词
Galectin-7; ovarian cancer; siRNA; prognosis; SQUAMOUS-CELL CARCINOMAS; HYPOPHARYNGEAL CANCER; P53-INDUCED GENE-1; TUMOR PROGRESSION; EXPRESSION; MATRIX-METALLOPROTEINASE-9; IDENTIFICATION; PROLIFERATION; TUMORIGENESIS; ACCUMULATION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Galectin-7 (GAL-7) has been highlighted as an important marker in many types of cancers by either inhibiting or promoting tumor growth. In this novel study, we assessed the association of GAL-7 with clinicopathological variables and survival outcomes in epithelial ovarian cancer (EOC) and investigated the role of GAL-7 in proliferation of ovarian cancer cell lines. Materials and Methods: The expression of GAL-7 was determined in 63 formalin-fixed, paraffin-embedded EOC tissues using an immunohistochemical method and we compared various associated clinicopathological factors. To evaluate the role of GAL-7 in cell proliferation, we performed proliferation assays with GAL-7 siRNA using ovarian cancer cell lines, including A2780-PAR cells. Results: Immunohistochemical analysis revealed that GAL-7 expression was primarily detected in nuclei and occasionally in the nucleus and cytoplasm. High GAL-7 expression was associated with greater age (p=0.016), high mortality (p=0.025), and poor overall survival outcome (p=0.029). In addition, the residual tumor volume was larger in the high-expression group compared to the low-expression group, although the difference was not statistically significant (p=0.059). Down-regulation of GAL-7 using siRNA resulted in the inhibition of cell proliferation of A2780-PAR cells. Conclusion: We observed that high GAL-7 might be associated with poor survival outcome in patients with EOC, and may be fitnctionally involved in cell proliferation.
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页码:1555 / 1561
页数:7
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