The ubiquitin-conjugating enzyme E2-EPF is overexpressed in cervical cancer and associates with tumor growth

التفاصيل البيبلوغرافية
العنوان: The ubiquitin-conjugating enzyme E2-EPF is overexpressed in cervical cancer and associates with tumor growth
المؤلفون: Hirotaka Nishi, Mei-Lu Bian, Jing Liang, Hiroe Ito, Chinatsu Higuma, Toru Sasaki, Keiichi Isaka
المصدر: Oncology Reports. 28:1519-1525
بيانات النشر: Spandidos Publications, 2012.
سنة النشر: 2012
مصطلحات موضوعية: Cancer Research, Paclitaxel, Topoisomerase Inhibitors, Mice, Nude, Uterine Cervical Neoplasms, Biology, medicine.disease_cause, Mice, Reference Values, Cell Line, Tumor, medicine, Animals, Humans, RNA, Small Interfering, Promoter Regions, Genetic, Etoposide, Cell Proliferation, Cervical cancer, Gene knockdown, Oncogene, Cancer, General Medicine, Cell cycle, Hypoxia-Inducible Factor 1, alpha Subunit, medicine.disease, Gene Expression Regulation, Neoplastic, Oncology, Doxorubicin, Gene Knockdown Techniques, Ubiquitin-Conjugating Enzymes, Carcinoma, Squamous Cell, Cancer research, Female, Topotecan, Topoisomerase I Inhibitors, Carcinogenesis, medicine.drug
الوصف: We found that the ubiquitin-conjugating enzyme E2-EPF mRNA is highly expressed in cervical squamous cancer relative to normal tissues and its expression levels positively correlate with clinical stage. Reduction of E2-EPF protein levels by >80% using shRNA decreases the expression levels of HIF-1α, and the proliferation, invasion and tumorigenicity of SiHa, a cervical squamous cancer cell line. E2-EPF knockdown also increases the chemosensitivity to topoisomerase I inhibitor (topotecan) and II (etoposide and doxorubicin). Our results suggest that E2-EPF is associated with the growth and aggressivity of cervical tumor cells. Targeting the E2-EPF pathway may have potential clinical applications for the treatment of cervical cancer.
تدمد: 1791-2431
1021-335X
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ac675516234f105fd9f4ad1ab3aecbb
https://doi.org/10.3892/or.2012.1949
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....5ac675516234f105fd9f4ad1ab3aecbb
قاعدة البيانات: OpenAIRE