Title : Therapeutic targeting of PELP1 prevents ovarian cancer growth and metastasis.

Pub. Date : 2011 Apr 15

PMID : 21421858






6 Functional Relationships(s)
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1 In this study, we examined whether the nuclear receptor coregulator PELP1 (proline-, glutamic acid-, leucine-rich protein-1) contributes to progression and metastatic potential of ovarian cancer cells and determined whether blocking of the PELP1 signaling axis had a therapeutic effect. Proline proline, glutamate and leucine rich protein 1 Homo sapiens
2 Therapeutic potential of PELP1-siRNA in vivo was determined using a nanoliposomal formulation of PELP1-siRNA-DOPC (1,2-dioleoyl-sn-glycero-3-phosphatidylcholine) administered systemically in a xenograft model. 1,2-oleoylphosphatidylcholine proline, glutamate and leucine rich protein 1 Homo sapiens
3 Therapeutic potential of PELP1-siRNA in vivo was determined using a nanoliposomal formulation of PELP1-siRNA-DOPC (1,2-dioleoyl-sn-glycero-3-phosphatidylcholine) administered systemically in a xenograft model. 1,2-oleoylphosphatidylcholine proline, glutamate and leucine rich protein 1 Homo sapiens
4 Therapeutic potential of PELP1-siRNA in vivo was determined using a nanoliposomal formulation of PELP1-siRNA-DOPC (1,2-dioleoyl-sn-glycero-3-phosphatidylcholine) administered systemically in a xenograft model. 1,2-oleoylphosphatidylcholine proline, glutamate and leucine rich protein 1 Homo sapiens
5 Therapeutic potential of PELP1-siRNA in vivo was determined using a nanoliposomal formulation of PELP1-siRNA-DOPC (1,2-dioleoyl-sn-glycero-3-phosphatidylcholine) administered systemically in a xenograft model. 1,2-oleoylphosphatidylcholine proline, glutamate and leucine rich protein 1 Homo sapiens
6 CONCLUSION: The results suggest that PELP1 signaling axis is a potential druggable target and liposomal PELP1-siRNA-DOPC could be used as a novel drug to prevent or treat ovarian metastasis. 1,2-oleoylphosphatidylcholine proline, glutamate and leucine rich protein 1 Homo sapiens