2010
DOI: 10.1016/j.imlet.2010.04.006
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Retinoblastoma protein-interacting zinc finger 1 (RIZ1) participates in RANKL-induced osteoclast formation via regulation of NFATc1 expression

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Cited by 10 publications
(8 citation statements)
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“…Because cancer undergoes metastasis and spreads to other organs at late stages, we speculated that RIZ1 might play an important role in tumor metastasis, although increases in mRNA expression do not always translate proportionally into protein expression levels. Our speculation was in line with two previous observations 23, 24.…”
Section: Resultssupporting
confidence: 93%
See 1 more Smart Citation
“…Because cancer undergoes metastasis and spreads to other organs at late stages, we speculated that RIZ1 might play an important role in tumor metastasis, although increases in mRNA expression do not always translate proportionally into protein expression levels. Our speculation was in line with two previous observations 23, 24.…”
Section: Resultssupporting
confidence: 93%
“…The second observation was that RIZ1 may augment the expression of nuclear factor of activated T cell 1 (NFATc1) 24, which induces breast cancer cell invasion via cyclooxygenase-2 29. Therefore, we hypothesize that RIZ1 might possess dual functions during tumor progression, acting as a tumor suppressor to induce apoptosis in the early stages and a tumor promoter to induce metastasis in late stages.…”
Section: Resultsmentioning
confidence: 99%
“…TRAP staining was carried out according to the manufacturer's instruction as described elsewhere [23]. The images were taken with a digital camera attached to the microscope.…”
Section: Trap Stainingmentioning
confidence: 99%
“…Retinoblastoma protein-interacting zinc finger 1 (RIZ1) protein also participates in RANKLinduced osteoclastogenesis, [114] binding with both retinoblastoma protein and estrogen receptors and reportedly involved in osteosarcoma. [115][116][117] RIZ1 expression increases under RANKL induction at 24 hours, and RIZ1 siRNA-transfected RAW 264.7 cells showed significantly inhibited NFATc1 activation 3 days post-RANKL and M-CSF treatment, but with no significant influence on TRAF6 expression.…”
Section: Osteoclastogenesismentioning
confidence: 99%