Downregulation of miR-193a-3p inhibits cell growth and migration in renal cell carcinoma by targeting PTEN
Published 2017 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Downregulation of miR-193a-3p inhibits cell growth and migration in renal cell carcinoma by targeting PTEN
Authors
Keywords
-
Journal
TUMOR BIOLOGY
Volume 39, Issue 6, Pages 101042831771195
Publisher
SAGE Publications
Online
2017-06-22
DOI
10.1177/1010428317711951
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Renal cancer
- (2016) Umberto Capitanio et al. LANCET
- Downregulation of microRNA-193-3p inhibits tumor proliferation migration and chemoresistance in human gastric cancer by regulating PTEN gene
- (2016) Bin Jian et al. TUMOR BIOLOGY
- miR-155 regulates the proliferation and invasion of clear cell renal cell carcinoma cells by targeting E2F2
- (2016) Yu Gao et al. Oncotarget
- A Systematic Review of Sequencing and Combinations of Systemic Therapy in Metastatic Renal Cancer
- (2015) Laurence Albiges et al. EUROPEAN UROLOGY
- MicroRNA-454 functions as an oncogene by regulating PTEN in uveal melanoma
- (2015) Lei Sun et al. FEBS LETTERS
- miR-181a mediates metabolic shift in colon cancer cells via the PTEN/AKT pathway
- (2014) Zhonghua Wei et al. FEBS LETTERS
- Tissue mechanics modulate microRNA-dependent PTEN expression to regulate malignant progression
- (2014) Janna K Mouw et al. NATURE MEDICINE
- MicroRNA-193a-3p and -5p suppress the metastasis of human non-small-cell lung cancer by downregulating the ERBB4/PIK3R3/mTOR/S6K2 signaling pathway
- (2014) T Yu et al. ONCOGENE
- The DNA methylation-regulated miR-193a-3p dictates the multi-chemoresistance of bladder cancer via repression of SRSF2/PLAU/HIC2 expression
- (2014) L Lv et al. Cell Death & Disease
- Ionizing radiation-inducible microRNA miR-193a-3p induces apoptosis by directly targeting Mcl-1
- (2013) Jeong-Eun Kwon et al. APOPTOSIS
- Potentiality of a triple microRNA classifier: miR-193a-3p, miR-23a and miR-338-5p for early detection of colorectal cancer
- (2013) Fung Lin Yong et al. BMC CANCER
- MicroRNA-21 mediates the rapamycin-induced suppression of endothelial proliferation and migration
- (2013) Chongying Jin et al. FEBS LETTERS
- Novel Immunotherapeutic Strategies in Development for Renal Cell Carcinoma
- (2012) Brant A. Inman et al. EUROPEAN UROLOGY
- MiR-210 expression in tumor tissue and in vitro effects of its silencing in renal cell carcinoma
- (2012) Martina Redova et al. TUMOR BIOLOGY
- MicroRNA profiling with correlation to gene expression revealed the oncogenic miR-17-92 cluster to be up-regulated in osteosarcoma
- (2012) Daniel Baumhoer et al. Cancer Genetics
- DNA Methylation-regulated miR-193a-3p Dictates Resistance of Hepatocellular Carcinoma to 5-Fluorouracil via Repression of SRSF2 Expression
- (2011) Kelong Ma et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Involvement of miR-21 in resistance to daunorubicin by regulating PTEN expression in the leukaemia K562 cell line
- (2010) Haitao Bai et al. FEBS LETTERS
- Expression of miRNA-106b in conventional renal cell carcinoma is a potential marker for prediction of early metastasis after nephrectomy
- (2010) Ondrej Slaby et al. JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH
- A Diagnostic Assay Based on MicroRNA Expression Accurately Identifies Malignant Pleural Mesothelioma
- (2010) Hila Benjamin et al. JOURNAL OF MOLECULAR DIAGNOSTICS
- TGF-β activates Akt kinase through a microRNA-dependent amplifying circuit targeting PTEN
- (2009) Mitsuo Kato et al. NATURE CELL BIOLOGY
- MicroRNA Expression Profiling in Human Ovarian Cancer: miR-214 Induces Cell Survival and Cisplatin Resistance by Targeting PTEN
- (2008) H. Yang et al. CANCER RESEARCH
Become a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get StartedAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started