E
Ederlyn Q. Dia
Researcher at University of California, Los Angeles
Publications - 4
Citations - 2015
Ederlyn Q. Dia is an academic researcher from University of California, Los Angeles. The author has contributed to research in topics: PTEN & Epidermal growth factor receptor. The author has an hindex of 4, co-authored 4 publications receiving 1965 citations.
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Journal ArticleDOI
Molecular determinants of the response of glioblastomas to EGFR kinase inhibitors.
Ingo K. Mellinghoff,Maria Y. Wang,Igor Vivanco,Daphne A. Haas-Kogan,Shaojun Zhu,Ederlyn Q. Dia,Kan V. Lu,Koji Yoshimoto,Julie H. Y Huang,Dennis J. Chute,Bridget L. Riggs,Steve Horvath,Linda M. Liau,Webster K. Cavenee,P. Nagesh Rao,Rameen Beroukhim,Rameen Beroukhim,Rameen Beroukhim,Timothy C. Peck,Timothy C. Peck,Timothy C. Peck,Jeffrey C. Lee,Jeffrey C. Lee,Jeffrey C. Lee,William R. Sellers,William R. Sellers,William R. Sellers,David Stokoe,Michael D. Prados,Timothy F. Cloughesy,Charles L. Sawyers,Paul S. Mischel +31 more
TL;DR: Coexpression of EGFRvIII and PTEN by glioblastoma cells is associated with responsiveness to EGFR kinase inhibitors, and effects of the molecular abnormalities in vitro are identified.
Journal ArticleDOI
Mammalian target of rapamycin inhibition promotes response to epidermal growth factor receptor kinase inhibitors in PTEN-deficient and PTEN-intact glioblastoma cells
Maria Y. Wang,Kan V. Lu,Shaojun Zhu,Ederlyn Q. Dia,Igor Vivanco,Gregory M. Shackleford,Webster K. Cavenee,Ingo K. Mellinghoff,Timothy F. Cloughesy,Charles L. Sawyers,Paul S. Mischel +10 more
TL;DR: Combined EGFR/mTOR kinase inhibition inhibits tumor cell growth and has an additive effect on inhibiting downstream PI3K pathway signaling and combination therapy provides added benefit in promoting cell death in PTEN-deficient tumor cells.
Journal ArticleDOI
Distinct transcription profiles of primary and secondary glioblastoma subgroups
Cho Lea Tso,William A. Freije,Allen Day,Zugen Chen,Barry Merriman,Ally Perlina,Yohan Lee,Ederlyn Q. Dia,Koji Yoshimoto,Paul S. Mischel,Linda M. Liau,Timothy F. Cloughesy,Stanley F. Nelson +12 more
TL;DR: Large-scale expression analyses were used to identify glioblastoma-associated genes (GAG) that are associated with a more malignant phenotype via comparison with lower-grade astrocytomas and highlight that the development of gene pathway-targeted therapies may need to be specifically tailored to each subtype of gliOBlastoma.
Journal ArticleDOI
Differential induction of glioblastoma migration and growth by two forms of pleiotrophin.
Kan V. Lu,Kimberly A. Jong,Gloria Y. Kim,Jatinder Singh,Ederlyn Q. Dia,Koji Yoshimoto,Maria Y. Wang,Timothy F. Cloughesy,Stanley F. Nelson,Paul S. Mischel +9 more
TL;DR: The presence and purification of two naturally occurring forms of PTN (18 and 15 kDa) that differentially promote glioblastoma migration and proliferation are reported on, indicating that thePTN18-PTPRZ1 and the PTN15-ALK signaling pathways represent potentially important therapeutic targets for glioblasts invasion and growth.