Elsevier

Neoplasia

Volume 12, Issue 9, September 2010, Pages 748-754
Neoplasia

Reactive Astrocytes Protect Melanoma Cells from Chemotherapy by Sequestering Intracellular Calcium through Gap Junction Communication Channels1

https://doi.org/10.1593/neo.10602Get rights and content
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open access

Abstract

Brain metastases are highly resistant to chemotherapy. Metastatic tumor cells are known to exploit the host microenvironment for their growth and survival. We report here that melanoma brain metastases are surrounded and infiltrated by activated astrocytes, and we hypothesized that these astrocytes can play a role similar to their established ability to protect neurons from apoptosis. In coculture experiments, astrocytes, but not fibroblasts, reduced apoptosis in human melanoma cells treated with various chemotherapeutic drugs. This chemoprotective effect was dependent on physical contact and gap junctional communication between astrocytes and tumor cells. Moreover, the protective effect of astrocytes resulted from their sequestering calcium from the cytoplasm of tumor cells. These data suggest that brain tumors can, in principle, harness the neuroprotective effects of reactive astrocytes for their own survival and implicate a heretofore unrecognized mechanism for resistance in brain metastasis that might be of relevance in the clinic.

Abbreviations

BBB
blood-brain barrier
CBX
carbenoxolone
GFAP
glial fibrillary acidic protein
GFP
green fluorescent protein
GJC
gap junctional communication
5-FU
5-fluorouracil
PE
phycoerythrin
RFP
red fluorescent protein

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1

This work was supported in part by Cancer Center Support Core Grant CA16672 and grant 1U54-CA143837 (I.J.F.) from the National Cancer Institute, National Institutes of Health. Q.L. was supported by a predoctoral fellowship from The Rosalie B. Hite Foundation at the University of Texas MD Anderson Cancer Center.

2

Q.L. and K.B. share equal first authorship.