Unknown

Dataset Information

0

Stat3 upregulates leucine-rich repeat-containing g protein-coupled receptor 4 expression in osteosarcoma cells.


ABSTRACT: The activation of signal transducer and activator of transcription 3 (Stat3) signaling is the common hallmark in various human cancers including osteosarcoma. In the present study, according to PCR-based microarrays using cDNA prepared from interleukin-6 (IL-6) treated osteosarcoma cells, we found that leucine-rich repeat-containing G protein-coupled receptor 4 (LGR4) was a transcriptional target of Stat3. Overexpression of Stat3 promoted LGR4 expression, while its deficiency using small interfering RNA (siRNA) reduced LGR4 expression. Furthermore, we identified a Stat3 binding motif located at -556 to -549 bp in the LGR4 promoter that is able to interact with Stat3. Thus, our results suggest a previously unknown Stat3-LGR4 molecular network, which may control osteosarcoma development and progression.

SUBMITTER: Liu J 

PROVIDER: S-EPMC3886594 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature

altmetric image

Publications

Stat3 upregulates leucine-rich repeat-containing g protein-coupled receptor 4 expression in osteosarcoma cells.

Liu Jia J   Wei Wei W   Guo Chang-An CA   Han Ning N   Pan Jian-feng JF   Fei Teng T   Yan Zuo-qin ZQ  

BioMed research international 20131225


The activation of signal transducer and activator of transcription 3 (Stat3) signaling is the common hallmark in various human cancers including osteosarcoma. In the present study, according to PCR-based microarrays using cDNA prepared from interleukin-6 (IL-6) treated osteosarcoma cells, we found that leucine-rich repeat-containing G protein-coupled receptor 4 (LGR4) was a transcriptional target of Stat3. Overexpression of Stat3 promoted LGR4 expression, while its deficiency using small interfe  ...[more]

Similar Datasets

| S-EPMC3887977 | biostudies-literature
| S-EPMC2775985 | biostudies-literature
| S-EPMC5602409 | biostudies-literature
| S-EPMC5633117 | biostudies-literature
| S-EPMC2002521 | biostudies-literature
| S-EPMC2932791 | biostudies-literature
| S-EPMC3724619 | biostudies-literature
| S-EPMC3356614 | biostudies-literature
| S-EPMC4030839 | biostudies-literature
| S-EPMC3049723 | biostudies-literature