Cited by 32Chemokine receptors and signalingPI3K/AKT/mTOR signaling in cancerProtein Kinase Regulation and GTPase Signaling

Short-term cellular memory tunes the signaling responses of the chemokine receptor CXCR4

Open access
Spinosa, Phillip C., Humphries, Brock A., Lewin Mejia, Daniela, Buschhaus, Johanna M., Linderman, Jennifer J., Luker, Gary D., Luker, Kathryn E.·2019·Science Signaling

Abstract

Recent signaling events determine how CXCR4 activates its downstream effector kinases.

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Crossref · 10.1126/scisignal.aaw4204

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  1. [64]Spinosa PC, Luker KE, Luker GD, Linderman JJ. The CXCL12/CXCR7 signaling axis, isoforms, circadian rhythms, and tumor cellular composition dictate gradients in tissue. PLoS One. 2017; 12(11): 1– 17. PMC5678865 29117251

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Authors
Spinosa, P. C., Humphries, B. A., Lewin Mejia, D., Buschhaus, J. M., Linderman, J. J., Luker, G. D., & Luker, K. E.
Affiliations
  • University of Michigan (US)
  • Department of Radiology Center for Molecular Imaging, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Corresponding author
  • Luker, Gary D.
  • Luker, Kathryn E.
Venue
Science Signaling
Published
2019-07-09
Volume
12
Issue
589
ISSN
  • 1937-9145 (ISSN-L)
  • 1945-0877
OpenAlex
W2961814895
Cited by
31
References
77
Citations by year
2026: 2 · 2025: 4 · 2024: 2 · 2023: 4 · 2022: 9 · 2021: 3 · 2020: 6 · 2019: 1
FWCI
1.99
Type
journal article
Language
en
Open access
Locations
  • Science Signaling (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Institutes of Health (R01CA196018, U01CA210152, R37CA222563, T32 EB005582)
Topics
  • Health Sciences › Medicine › Oncology › Chemokine receptors and signaling
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
Keywords
CXCR4, CXCL12, chemokine signaling, Akt signaling, ERK signaling, mTORC1, phosphatidylinositol 3-kinase, extrinsic noise, cell-to-cell variability, metastasis, single-cell signaling, kinase inhibitors, cancer therapy
MeSH terms
Mechanistic Target of Rapamycin Complex 1, Computer Simulation, Enzyme Activation, Humans, Microscopy, Fluorescence, Phosphorylation, Signal Transduction, Receptors, CXCR4, Phosphatidylinositol 3-Kinases, Cell Line, Tumor, Extracellular Signal-Regulated MAP Kinases, Proto-Oncogene Proteins c-akt, Chemokine CXCL12, Time-Lapse Imaging, Single-Cell Analysis

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