Li Jing, Song Lan-lin, Zhong Mei
Department of Gynecology and Obstetrics, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Zhonghua Zhong Liu Za Zhi. 2013 Mar;35(3):170-4. doi: 10.3760/cma.j.issn.0253-3766.2013.03.003.
To investigate the correlation of ZNF217 gene expression with the biological behavior of human ovarian cancer HO-8910 cells.
The expression of ZNF217 in ovarian carcinoma cell lines was detected by RT-PCR and Western blot, respectively. The biological behaviors of the transfectants were investigated by MTT, in vitro Boyden chamber and in vivo invasion assay, respectively.
RT-PCR and Western blotting revealed that transfection of ZNF217 into the HO-8910 cells significantly increased their proliferation along with markedly enhanced in vitro and in vivo invasion and metastatic abilities. MTT assay showed that the proliferation ability of pEGFP-N1-ZNF217/HO-8910 cells was significantly higher than that of pEGFP-N1/HO-8910 cells and HO-8910 cells (P < 0.001). The Boyden chamber assay showed that the numbers of migrating pEGFP-N1-ZNF217/HO-8910, pEGFP-N1/HO-8910 and HO-8910 cells were (141.25 ± 13.91) cells/200×field, (82.50 ± 11.73) cells/200×field and (81.75 ± 12.12)cells/200×field, with a significant difference between them (F = 29.247, P < 0.001). The nude mouse experiment showed that the in vivo tumor formation ability of pEGFP-N1-ZNF217/HO-8910 cells was significantly higher than that of pEGFP-N1/HO-8910 cells (P < 0.001).
ZNF217 gene plays an important role in the invasion and metastasis of ovarian cancer. ZNF217 gene expression may be a useful marker indicating invasion and metastasis of ovarian cancer.
探讨ZNF217基因表达与人类卵巢癌HO - 8910细胞生物学行为的相关性。
分别采用RT - PCR和蛋白质免疫印迹法检测ZNF217在卵巢癌细胞系中的表达。分别通过MTT法、体外博伊登小室实验和体内侵袭实验研究转染细胞的生物学行为。
RT - PCR和蛋白质免疫印迹结果显示,将ZNF217转染至HO - 8910细胞后,其增殖能力显著增强,同时体外和体内侵袭及转移能力明显提高。MTT实验表明,pEGFP - N1 - ZNF217/HO - 8910细胞的增殖能力显著高于pEGFP - N1/HO - 8910细胞和HO - 8910细胞(P < 0.001)。博伊登小室实验显示,pEGFP - N1 - ZNF217/HO - 8910、pEGFP - N1/HO - 8910和HO - eq \o\ac(○,8910)细胞的迁移数分别为(141.25 ± 13.91)个细胞/200×视野、(82.50 ± 11.73)个细胞/200×视野和(81.75 ± 12.12)个细胞/200×视野,差异有统计学意义(F = 29.247,P < 0.001)。裸鼠实验表明,pEGFP - N1 - ZNF217/HO - 8910细胞的体内成瘤能力显著高于pEGFP - N1/HO - 8910细胞(P < 0.001)。
ZNF217基因在卵巢癌的侵袭和转移中起重要作用。ZNF217基因表达可能是提示卵巢癌侵袭和转移能力的有用标志物。