PAX2 Expression in Ovarian Cancer

被引:27
作者
Song, Huijuan [1 ,2 ]
Kwan, Suet-Yan [1 ,2 ]
Izaguirre, Daisy I. [1 ,2 ]
Zu, Zhifei [1 ]
Tsang, Yvonne T. [1 ]
Tung, Celestine S. [1 ]
King, Erin R. [1 ]
Mok, Samuel C. [1 ,2 ]
Gershenson, David M. [1 ]
Wong, Kwong-Kwok [1 ,2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Gynecol Oncol & Reprod Med, Houston, TX 77030 USA
[2] Univ Texas Houston, Grad Sch Biomed Sci, Canc Biol Program, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
PAX2; ovarian cancer; G0S2; WFDC1; GREM1; shRNA; RENAL-CELL CARCINOMA; KAPPA-B; PROTEIN; GENE; FAMILY; CARCINOGENESIS; PROLIFERATION; MUTATIONS; INTERACTS; KIDNEY;
D O I
10.3390/ijms14036090
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
PAX2 is one of nine PAX genes that regulate tissue development and cellular differentiation in embryos. However, the functional role of PAX2 in ovarian cancer is not known. Twenty-six ovarian cancer cell lines with different histology origins were screened for PAX2 expression. Two ovarian cancer cell lines: RMUGL (mucinous) and TOV21G (clear cell), with high PAX2 expression were chosen for further study. Knockdown PAX2 expression in these cell lines was achieved by lentiviral shRNAs targeting the PAX2 gene. PAX2 stable knockdown cells were characterized for cell proliferation, migration, apoptosis, protein profiles, and gene expression profiles. The result indicated that these stable PAX2 knockdown cells had reduced cell proliferation and migration. Microarray analysis indicated that several genes involved in growth inhibition and motility, such as G0S2, GREM1, and WFDC1, were up-regulated in PAX2 knockdown cells. On the other hand, over-expressing PAX2 in PAX2-negative ovarian cell lines suppressed their cell proliferation. In summary, PAX2 could have both oncogenic and tumor suppression functions, which might depend on the genetic content of the ovarian cancer cells. Further investigation of PAX2 in tumor suppression and mortality is warranted.
引用
收藏
页码:6090 / 6105
页数:16
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