دورية أكاديمية

LINC00441 promotes cervical cancer progression by modulating miR-450b-5p/RAB10 axis

التفاصيل البيبلوغرافية
العنوان: LINC00441 promotes cervical cancer progression by modulating miR-450b-5p/RAB10 axis
المؤلفون: Haiyan Han, Qingchun Shao, Xuejie Liu
المصدر: Cancer Cell International, Vol 20, Iss 1, Pp 1-14 (2020)
بيانات النشر: BMC, 2020.
سنة النشر: 2020
المجموعة: LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
LCC:Cytology
مصطلحات موضوعية: LINC00441, Cervical cancer, miR-450b-5p, RAB10, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Cytology, QH573-671
الوصف: Abstract Background As one of the most common gynaecological malignant tumors, cervical cancer (CC) has become an important public health issue. Emerging evidence has revealed long non-coding RNAs (lncRNAs) are crucial regulators of biological functions in cancers, including CC. And the oncogenic role of LINC00441 has been verified in hepatocellular carcinoma (HCC). But the molecular mechanism and biological functions of LINC00441 in CC remain unknown. Methods qRT-PCR analysis detected the expression of genes in CC tissues or cells. CCK-8, colony formation, flow cytometry, transwell, western blot assays as well as animal studies were conducted to analyze the function of LINC00441 in CC. Luciferase reporter, RIP and RNA pull down assays were applied to verify the binding relations among the indicated genes. Results LINC00441 was upregulated in CC tissues and cells. Further, LINC00441 depletion repressed cell proliferation and motility in vitro as well as tumor growth in vivo. LINC00441 could sponge miR-450b-5p to upregulate RAB10 expression. Finally, miR-450b-5p inhibitor or RAB10 upregulation counteracted LINC00441 knockdown-mediated function on the development of CC. Conclusions LINC00441 drives CC progression by targeting miR-450b-5p/RAB10 axis, which might provide new idea for researching CC-related molecular mechanism.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1475-2867
Relation: http://link.springer.com/article/10.1186/s12935-020-01400-x; https://doaj.org/toc/1475-2867
DOI: 10.1186/s12935-020-01400-x
URL الوصول: https://doaj.org/article/d00c03f38e6841eead77f748a6cc7bfa
رقم الأكسشن: edsdoj.00c03f38e6841eead77f748a6cc7bfa
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14752867
DOI:10.1186/s12935-020-01400-x