Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

CREB1, a direct target of miR-122, promotes cell proliferation and invasion in bladder cancer

10 Jul 2018

Abstract excerpt

Bladder cancer (BC) is a prevalent cancer, which arises from the epithelial lining of the urinary bladder. CAMP-response element binding protein (CREB1) acts as a transcription factor, which regulates cell transcription through phosphorylation and dephosphorylation. The purpose of this study was to explore how miR-122 worked in BC on cell proliferation and invasion. RT-qPCR was applied to evaluate the mRNA levels...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Bladder and Urothelial Cancer Treatments
Share to Cancer-related molecular mechanisms research
Share to MicroRNA in disease regulation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 30127997
DOI: 10.3892/ol.2018.9118

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

CREB1, a direct target of miR-122, promotes cell proliferation and invasion in bladder cancerPMID 30127997Read ↗

<i>OASIS/CREB3L1</i>is epigenetically silenced in human bladder cancer facilitating tumor cell spreading and migration<i>in vitro</i>Semantic proximity Read ↗

FATP2 activates PI3K/Akt/mTOR pathway by inhibiting ATF3 and promotes the occurrence and development of bladder cancerSemantic proximity Read ↗

LncRNA BLACAT1/miR-519d-3p/CREB1 Axis Mediates Proliferation, Apoptosis, Migration, Invasion, and Drug-Resistance in Colorectal Cancer ProgressionSemantic proximity Read ↗

CAB39 mediates epithelial-mesenchymal transition via activation of NF-κB signaling to facilitate bladder cancer invasion and metastasisSemantic proximity Read ↗

Hsa_circ_0102171 aggravates the progression of cervical cancer through targeting miR‐4465/CREBRF axisSemantic proximity Read ↗

c-Met and CREB1 are involved in miR-433-mediated inhibition of the epithelial–mesenchymal transition in bladder cancer by regulating Akt/GSK-3β/Snail signalingSemantic proximity Read ↗

Upregulated lncRNA-UCA1 contributes to metastasis of bile duct carcinoma through regulation of miR-122/CLIC1and activation of the ERK/MAPK signaling pathwaySemantic proximity Read ↗

DHCR7 promotes tumorigenesis via activating PI3K/AKT/mTOR signalling pathway in bladder cancerSemantic proximity Read ↗

Quantitative Proteomics of Urinary Bladder Cancer Cell Lines Identify UAP1 as a Potential Therapeutic TargetSemantic proximity Read ↗

Control of CREB expression in tumors: from molecular mechanisms and signal transduction pathways to therapeutic targetSemantic proximity Read ↗

Exosome-transmitted microRNA-133b inhibited bladder cancer proliferation by upregulating dual-specificity protein phosphatase 1.Semantic proximity Read ↗

Identification of Novel Biomarkers and Candidate Drug in Ovarian CancerSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.