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Chemotherapy-mediated miR-29b expression inhibits the invasion and angiogenesis of cervical cancer
- Source :
- Oncotarget
- Publication Year :
- 2016
-
Abstract
- // Yunyun Li 1, * , Zhongzu Zhang 2, * , Zhenghua Xiao 1 , Ying Lin 1 , Tangshu Luo 1 , Qin Zhou 3 , Xiaojing Zhang 1 1 Department of Gynecology and Obstetrics, The Yongchuan Hospital of Chongqing Medical University, Chongqing 402160, PR China 2 Department of Orthopedics, The Yongchuan Hospital of Chongqing Medical University, Chongqing 402160, PR China 3 Department of Gynecology and Obstetrics, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, PR China * These authors contributes to this work Correspondence to: Qin Zhou, email: zhouqin_doctor@126.com Xiaojing Zhang, email: zhangxj_gyn@163.com Keywords: cervical cancer, miR-29b, STAT3, chemotherapy, EMT Received: November 14, 2016 Accepted: January 11, 2017 Published: January 19, 2017 ABSTRACT Radiotherapy combined with platinum-based chemotherapy is the standard-of-care of locally advanced cervical cancer (CC) patients, while nearly 50% of patients do not respond to standard chemotherapy. Thus, identification of relative molecules participated in chemotherapy might provide new insights in the treatment of CC. In this study, we found a cohort of miRNAs were dysregulated upon treatment with cisplatin, among of which miR-29b was the most upregulated one. We further detected its expression in CC tissues, and found that miR-29b was significantly suppressed in CC and its precancerous lesions, HSIL tissues, and was negatively related with tumor invasion. However, upon treatment with cisplatin, the expression of miR-29b was significantly up-regulated. The biological function assays showed that overexpression of miR-29b suppressed the invasion, EMT procedure and angiogenesis of cervical cancer cells in vitro and inhibited tumor growth and neovascularization in vivo through targeting STAT3 signal pathway. While, inhibition of miR-29b could prevent the cisplatin-induced epithelial features, cell movement and angiogenesis of CC cells, which means miR-29b/STAT3 axis participates in the chemotherapy of cisplatin in CC. Collectively, our data suggest that chemotherapy-mediated miR-29b expression participates in the initiation and progression of cervical cancer through suppressing the proliferation, EMT procedure and angiogenesis of cervical cancer cells by targeting STAT3 signal pathway.
- Subjects :
- 0301 basic medicine
Male
Pathology
Angiogenesis
cervical cancer
medicine.medical_treatment
Uterine Cervical Neoplasms
chemotherapy
Neovascularization
STAT3
0302 clinical medicine
Cell Movement
Medicine
3' Untranslated Regions
Cervical cancer
Mice, Inbred BALB C
biology
Neovascularization, Pathologic
Reverse Transcriptase Polymerase Chain Reaction
EMT
Up-Regulation
Gene Expression Regulation, Neoplastic
Oncology
030220 oncology & carcinogenesis
Female
medicine.symptom
medicine.drug
Signal Transduction
Research Paper
Adult
STAT3 Transcription Factor
medicine.medical_specialty
Blotting, Western
Transplantation, Heterologous
Mice, Nude
Antineoplastic Agents
03 medical and health sciences
Cell Line, Tumor
microRNA
Animals
Humans
Neoplasm Invasiveness
Cisplatin
Chemotherapy
business.industry
miR-29b
medicine.disease
Radiation therapy
MicroRNAs
030104 developmental biology
Cancer research
biology.protein
business
Precancerous Conditions
HeLa Cells
Subjects
Details
- ISSN :
- 19492553
- Volume :
- 8
- Issue :
- 9
- Database :
- OpenAIRE
- Journal :
- Oncotarget
- Accession number :
- edsair.doi.dedup.....0917a57cfee6a3f5590d3bfe56af7420