WT1/EGR1-mediated control of STIM1 expression and function in cancer cells

23Citations
Citations of this article
29Readers
Mendeley users who have this article in their library.

Abstract

There have been numerous publications linking Ca2+ signaling and cancer, however, a clear explanation for this link has remained elusive. We recently identified the oncogenes/tumor suppressors Wilms Tumor Suppressor 1 (WT1) and Early Growth Response 1 (EGR1) as regulators of the expression of STIM1, an essential regulator of Ca2+ entry in non-excitable cells. The current review focuses on the literature defining both differential Ca 2+ signaling and WT1/EGR1 expression patterns in 5 specific cancer subtypes: Acute Myeloid Leukemia, Wilms Tumor, breast cancer, glioblastoma and prostate cancer. For each tumortype, we have assessed how specific changes in WT1 and EGR1 expression might contribute to aberrant Ca2+ homeostasis as well as the therapeutic potential of these observations.

Author supplied keywords

Cite

CITATION STYLE

APA

Ritchie, M. F., Zhou, Y., & Soboloff, J. (2011). WT1/EGR1-mediated control of STIM1 expression and function in cancer cells. Frontiers in Bioscience, 16(7), 2402–2415. https://doi.org/10.2741/3862

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free