Targeting the Cohesive Cluster Phenotype in Chordoma via β1 Integrin Increases Ionizing Radiation Efficacy.
AuthorHarryman, William L
Gard, Jaime M C
Pond, Kelvin W
Simpson, Skyler J
Heppner, Lucas H
Little, Andrew S
Eschbacher, Jennifer M
Cress, Anne E
AffiliationUniv Arizona, Canc Ctr, 1515 N Campbell Ave, Tucson, AZ 85724 USA
Univ Arizona, Dept Cellular & Mol Med, 1515 N Campbell Ave, Tucson, AZ 85724 USA
Univ Arizona, Coll Med, Med Student Res Program, 1515 N Campbell Ave, Tucson, AZ 85724 USA
Univ Arizona, Canc Biol Res Program, 1515 N Campbell Ave, Tucson, AZ 85724 USA
MetadataShow full item record
PublisherELSEVIER SCIENCE INC
CitationHarryman WL, Gard JMC, Pond KW, et al. Targeting the Cohesive Cluster Phenotype in Chordoma via β1 Integrin Increases Ionizing Radiation Efficacy. Neoplasia (New York, NY). 2017;19(11):919-927. doi:10.1016/j.neo.2017.08.005.
Rights© 2017 The Authors. Published by Elsevier Inc. on behalf of Neoplasia Press, Inc. This is an open access article under theCCBY-NC-NDlicense (http://creativecommons.org/licenses/by-nc-nd/4.0/). 1476-5586
Collection InformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at email@example.com.
AbstractChordoma is a rare, radiation-resistant, skull-base and spinal tumor with high local recurrence containing mixed cell-adhesion phenotypes. We characterized DNA damage response (DDR) signaling (γH2AX, pKAP1, pATM) and survival response to ionizing radiation (IR) in human chordoma samples (42 resections, 23 patients) to test if blocking cell adhesion sensitizes U-CH1 tumor cells to IR. U-CH1 cells expressed brachyury, YAP, and laminin adhesion receptors (CD49c, CD49f, CD44), and approximately 15% to 20% of U-CH1 cells featured an α6 integrin-dependent (CD49f) cohesive cluster phenotype, which confers therapeutic resistance and aids metastasis. DDR to IR in U-CH1 cells was compared to normal prostate epithelial (PrEC) and tumor cells (DU145). Flow cytometry showed a dose- and time-dependent increase in γH2AX and pKAP1 expression in all cell lines. However, nearly 50% of U-CH1 cells exhibited nonresponsive phenotype to IR (measured by γH2AX and pKAP1) independent of cell cycle status. Immunofluorescence microscopy verified that only 15% of U-CH1 clustered cells were γH2AX or pKAP1 positive (versus 80% of nonclustered cells) 2 hours following 2-Gy IR. Conversely, both tumor cell lines were uniformly defective in pATM response. HYD1, a synthetic ECM ligand, inhibited DDR through an unresolved γH2AX response. β1 integrin-blocking antibody (AIIB2) decreased cell survival 50% itself and approximately doubled the IR-induced cell kill at all IR doses observed at 2 and 4 weeks posttreatment. These results suggest that a heterogeneity of DDR to IR exists within a chordoma population. Blocking integrin function alone and/or as an adjuvant to IR may eradicate chordomas containing the cohesive cluster phenotype.
NoteOpen access journal.
VersionFinal published version
SponsorsNational Institutes Health [P30CA23074, RO1CA159406, T32CA09213, T35HL007479]