4.5 Article

Targeting Aurora Kinase A enhances radiation sensitivity of atypical teratoid rhabdoid tumor cells

Journal

JOURNAL OF NEURO-ONCOLOGY
Volume 107, Issue 3, Pages 517-526

Publisher

SPRINGER
DOI: 10.1007/s11060-011-0795-y

Keywords

Atypical teratoid rhabdoid tumor; ATRT; Aurora Kinase A

Funding

  1. Department of Pediatrics
  2. Children's Hospital Denver
  3. Morgan Adams Foundation
  4. National Institutes of Health [KO8 NS59790]

Ask authors/readers for more resources

Atypical teratoid/ rhabdoid tumors (ATRT) are rare, highly malignant, embryonal CNS tumors with a poor prognosis. Therapy relies on highly toxic chemotherapy and radiotherapy. To improve outcomes and decrease morbidity, more targeted therapy is required. Gene expression analysis revealed elevated expression of multiple kinases in ATRT tissues. Aurora Kinase A was one of the candidate kinases. The objective of this study was to evaluate the impact of Aurora Kinase A inhibition in ATRT cell lines. Our analysis revealed that inhibition of Aurora Kinase A induces cell death in ATRT cells and the small molecule inhibitor MLN 8237 sensitizes these cells to radiation. Furthermore, inhibition of Aurora Kinase A resulted in decreased activity of pro-proliferative signaling pathways. These data indicate that inhibition of Aurora Kinase A is a promising small molecule target for ATRT therapy.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available