The use of compounds is described which are capable of functionally blocking at least one of the genes chosen from the group composed of EphA1, EphA2, EphA8, EphB2, CSF1R, VEGFR2, RAMP2, RAMP3, CLRN1, MAPK4, PIK3C2A, PIK3CG, GSK3alpha, GSK3beta, IRAK3, DAPK1, JAK1, PIM1, TRB3, BTG1, LATS1, LIMK2, MYLK, PAK1, PAK2, CDC2, BTK, PNRC2, NCOA4, NR2C1, TPR, RBBP8, TRPC7, FXYD1, ERN1, PRSS16, RPS3, CCL23 and SERPINE1, for the manufacture of a medicament destined to diminish the resistance to chemotherapeutic drugs in the therapeutic treatment of epithelial tumour pathologies. Also described is a method for the determination of the drug resistance in tumour cells, as well as a method forthe identification of tumour stem cells.

Lavitrano, M., Grassilli, E., Helin, K. (2008)Modulator compounds of the drug resistance in epithelial tumour cells. . Brevetto No. CA 2680589.

Modulator compounds of the drug resistance in epithelial tumour cells

LAVITRANO, MARIALUISA;GRASSILLI, EMANUELA;
2008

Abstract

The use of compounds is described which are capable of functionally blocking at least one of the genes chosen from the group composed of EphA1, EphA2, EphA8, EphB2, CSF1R, VEGFR2, RAMP2, RAMP3, CLRN1, MAPK4, PIK3C2A, PIK3CG, GSK3alpha, GSK3beta, IRAK3, DAPK1, JAK1, PIM1, TRB3, BTG1, LATS1, LIMK2, MYLK, PAK1, PAK2, CDC2, BTK, PNRC2, NCOA4, NR2C1, TPR, RBBP8, TRPC7, FXYD1, ERN1, PRSS16, RPS3, CCL23 and SERPINE1, for the manufacture of a medicament destined to diminish the resistance to chemotherapeutic drugs in the therapeutic treatment of epithelial tumour pathologies. Also described is a method for the determination of the drug resistance in tumour cells, as well as a method forthe identification of tumour stem cells.
Si
siRNA, drug resistance, epithelial tumors
Human necessities
Rilevanza internazionale
CA 2680589
18-set-2008
Altro titolare
Lavitrano, M; Grassilli, E; Helin, K
Lavitrano, M., Grassilli, E., Helin, K. (2008)Modulator compounds of the drug resistance in epithelial tumour cells. . Brevetto No. CA 2680589.
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/61772
Citazioni
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
Social impact