4.3 Review

Improved Anti-Tumor Activity of Novel Highly Bioactive Liposome-Bound TRAIL in Breast Cancer Cells

Journal

RECENT PATENTS ON ANTI-CANCER DRUG DISCOVERY
Volume 11, Issue 2, Pages 197-214

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1574892811666160229121544

Keywords

Breast cancer; DR5; flavopiridol; immunotherapy; lipid nanoparticles; TRAIL

Funding

  1. Instituto de Salud Carlos III/Fondo Europeo de Desarrollo Regional [PI13/00416]
  2. Fundacion Sandra Ibarra [FSI 2011-003]
  3. Ministerio de Economia y Competitividad [SAF2013-48626-C2-1-R, DPI2011-28262-C04-01]
  4. MICROANGIOTHECAN
  5. CIBER-IMIBIC
  6. Gobierno de Aragon
  7. EMBO short-term fellowship

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Background: Apo2-ligand/TRAIL, a member of the TNF cytokine superfamily capable of inducing apoptosis on tumor cells while sparing normal cells, is a promising anti-tumor agent. However, about 50% of human cancer are TRAIL resistant. Consequently, future TRAIL-based therapies will require the use of novel highly bioactive forms of TRAIL and/or the addition of sensitizing agents to TRAIL-induced apoptosis. Recently, we demonstrated that artificial lipid nanoparticles coated with bioactive TRAIL (LUV-TRAIL) greatly improved TRAIL activity and were able to induce apoptosis in chemoresistant hematological tumor cells. Objective: In this study, we have tested LUV-TRAIL-pro-apoptotic potential in human breast cancer. Method: Comparative analysis of cytotoxicity induced by sTRAIL and LUV-TRAIL was performed using several human breast tumor cell lines with different sensitivity to TRAIL. In vivo anti-tumor activity of LUV-TRAIL was also studied using a xeno-graft tumor model. Results: LUV-TRAIL improved not only sTRAIL in vitro cytotoxicity in all breast tumor cell lines tested but also showed more anti-tumor activity than sTRAIL in an in vivo xeno-graft tumor model. On the other hand, the concomitant treatment of LUV-TRAIL with the sensitizing agent flavopiridol (FVP) induced a higher level of cell death in TRAIL-resistant cell lines. TRAIL-sensitization induced by FVP was mediated by DR5 up-regulation, and interestingly TRAIL-apoptotic signaling was completely shifted towards DR5 upon FVP treatment. LUV-TRAIL could especially take advantage of this DR5 up-regulation, while sTRAIL was not able. Conclusion: To date, no special attention had been paid to this aspect of FVP-induced TRAIL-sensitization, may be because sTRAIL used were not able to take advantage of this DR5 up-regulation. Hence, LUV-TRAIL could be a better choice than sTRAIL to be used in combination with anti-tumor drugs inducing DR5 over-expression, since LUV-TRAIL is especially effective activating this death-receptor.

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