Expression of Transcription Factor FOXC2 in Cervical Cancer and Effects of Silencing on Cervical Cancer Cell Proliferation
| Autor: | Wen-Jing Shao, Wei-guo Deng, Yuan Quan, Chun-Hua Zheng, Yi-yang Li, Yan Fu |
|---|---|
| Rok vydání: | 2014 |
| Předmět: |
Cancer Research
Pathology medicine.medical_specialty Epidemiology Uterine Cervical Neoplasms Antigens CD34 Adenocarcinoma Biology Sincalide Metastasis HeLa Cell Movement Cell Line Tumor medicine Carcinoma Humans Neoplasm Invasiveness RNA Small Interfering Cervix Cell Proliferation Cervical cancer Neovascularization Pathologic Public Health Environmental and Occupational Health Cancer Forkhead Transcription Factors Middle Aged medicine.disease biology.organism_classification Gene Expression Regulation Neoplastic medicine.anatomical_structure Oncology Lymphatic Metastasis Carcinoma Squamous Cell Cancer research biology.protein Female RNA Interference FOXC2 HeLa Cells |
| Zdroj: | Asian Pacific Journal of Cancer Prevention. 15:1589-1595 |
| ISSN: | 1513-7368 |
| DOI: | 10.7314/apjcp.2014.15.4.1589 |
| Popis: | Objective: Forkhead box C2 (FOXC2) is a member of the winged helix/forkhead box (Fox) family of transcription factors. It has been suggested to regulate tumor vasculature, growth, invasion and metastasis, although it has not been studied in cervical cancer. Here, we analyzed FOXC2 expression in cervical tissues corresponding to different stages of cervical cancer development and examined its correlation with clinicopathological characteristics. In addition, we examined the effects of targeting FOXC2 on the biological behavior of human cervical cancer cells. Methods: The expression of FOXC2 in normal human cervix, CIN I-III and cervical cancer was examined by immunohistochemistry and compared among the three groups and between cervical cancers with different pathological subtypes. Endogenous expression of FOXC2 was transiently knocked down in human Hela and SiHa cervical cells by siRNA, and cell viability and migration were examined by scratch and CCK8 assays, respectively. Results: In normal cervical tissue the frequency of positive staining was 25% (10/40 cases), with a staining intensity (PI) of 0.297±0.520, in CIN was 65% (26/40cases), with a PI of 3.00±3.29, and in cancer was 91.8% (68/74 cases), with a PI of 5.568 ±3.449. The frequency was 100% in adenocarcinoma (5/5 cases) and 91.3% in SCCs (63/69 cases). The FOXC2 positive expression rate was 88.5% in patients with cervical SCC stage I and 100% in stage II, showing significant differences compared with normal cervix and CIN. With age, pathologic differentiation degree and tumor size, FOXC2 expression showed no significant variation. On transient transfection of Hela and SiHa cells, FOXC2-siRNA inhibition rates were 76.2% and 75.7%; CCK8 results showed reduced proliferation and relative migration (in Hela cells from 64.5±3.16 to 49.5±9.24 and in SiHa cells from 60.1±3.05 to 44.3±3.98) (P < 0.05). Conclusion: FOXC2 gene expression increases with malignancy, especially with blood vessel hyperplasia and invasion degree. Targeted silencing was associated with reduced cell proliferation as well as invasion potential. |
| Databáze: | OpenAIRE |
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