TY - JOUR
T1 - Novel "Elements" of immune suppression within the tumor microenvironment
AU - Gurusamy, Devikala
AU - Clever, David
AU - Eil, Robert
AU - Restifo, Nicholas P.
N1 - Funding Information:
This work was supported by the Intramural Research Program of the Center forCancer Research, NCI, NIH.We thank Suman K. Vodnala and Ping-Hsien Lee for helpful discussions and Jennifer Michalowski for excellent editorial input on this article. We are grateful to Richard Lee for histologic images of tumors and Erina He and Alan Hoofring for illustrations.
Publisher Copyright:
© 2017 American Association for Cancer Research.
PY - 2017/6/1
Y1 - 2017/6/1
N2 - Adaptive evolution has prompted immune cells to use a wide variety of inhibitory signals, many of which are usurped by tumor cells to evade immune surveillance. Although tumor immunologists often focus on genes and proteins as mediators of immune function, here we highlight two elements from the periodic table-oxygen and potassium-that suppress the immune system in previously unappreciated ways. While both are key to the maintenance of T-cell function and tissue homeostasis, they are exploited by tumors to suppress immuno-surveillance and promote metastatic spread. We discuss the temporal and spatial roles of these elements within the tumor microenvironment and explore possible therapeutic interventions for effective and promising anticancer therapies.
AB - Adaptive evolution has prompted immune cells to use a wide variety of inhibitory signals, many of which are usurped by tumor cells to evade immune surveillance. Although tumor immunologists often focus on genes and proteins as mediators of immune function, here we highlight two elements from the periodic table-oxygen and potassium-that suppress the immune system in previously unappreciated ways. While both are key to the maintenance of T-cell function and tissue homeostasis, they are exploited by tumors to suppress immuno-surveillance and promote metastatic spread. We discuss the temporal and spatial roles of these elements within the tumor microenvironment and explore possible therapeutic interventions for effective and promising anticancer therapies.
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U2 - 10.1158/2326-6066.CIR-17-0117
DO - 10.1158/2326-6066.CIR-17-0117
M3 - Article
C2 - 28576921
AN - SCOPUS:85020646766
SN - 2326-6066
VL - 5
SP - 426
EP - 433
JO - Cancer immunology research
JF - Cancer immunology research
IS - 6
ER -