TY - JOUR
T1 - Roles of Notch Signaling in the Tumor Microenvironment
AU - D’assoro, Antonino B.
AU - Leon‐ferre, Roberto
AU - Braune, Eike Benjamin
AU - Lendahl, Urban
N1 - Funding Information:
Funding: Work in the authors’ laboratories is supported by a grant from the Mayo‐KI breast cancer research program (AD, UL). AD is also supported by the Randy Shaver Foundation and UL by the Swedish Cancer Society and the Swedish Research Council. RL‐F is supported by CTSA Grant Num‐ ber KL2 TR002379 from the National Center for Advancing Translational Science (NCATS), and the Mayo Clinic Breast Cancer SPORE grant P50 CA116201, Career Enhancement Program, from the National Institutes of Health. Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH.
Funding Information:
Conflicts of Interest: U.L. holds a research grant from Merck KGaA but no personal remuneration. R.L.‐F. has conducted consulting activities for AstraZeneca and Gilead Sciences, outside of the scope of this work, with honoraria paid to the institution for research activities but no personal remuner‐ ation. Other authors declare no conflict of interest.
Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/6/1
Y1 - 2022/6/1
N2 - The Notch signaling pathway is an architecturally simple signaling mechanism, well known for its role in cell fate regulation during organ development and in tissue homeostasis. In keeping with its importance for normal development, dysregulation of Notch signaling is increasingly associated with different types of tumors, and proteins in the Notch signaling pathway can act as oncogenes or tumor suppressors, depending on the cellular context and tumor type. In addition to a role as a driver of tumor initiation and progression in the tumor cells carrying oncogenic mutations, it is an emerging realization that Notch signaling also plays a role in non‐mutated cells in the tumor microenvironment. In this review, we discuss how aberrant Notch signaling can affect three types of cells in the tumor stroma—cancer‐associated fibroblasts, immune cells and vascular cells—and how this influences their interactions with the tumor cells. Insights into the roles of Notch in cells of the tumor environment and the impact on tumor‐stroma interactions will lead to a deeper understanding of Notch signaling in cancer and inspire new strategies for Notch‐based tumor therapy.
AB - The Notch signaling pathway is an architecturally simple signaling mechanism, well known for its role in cell fate regulation during organ development and in tissue homeostasis. In keeping with its importance for normal development, dysregulation of Notch signaling is increasingly associated with different types of tumors, and proteins in the Notch signaling pathway can act as oncogenes or tumor suppressors, depending on the cellular context and tumor type. In addition to a role as a driver of tumor initiation and progression in the tumor cells carrying oncogenic mutations, it is an emerging realization that Notch signaling also plays a role in non‐mutated cells in the tumor microenvironment. In this review, we discuss how aberrant Notch signaling can affect three types of cells in the tumor stroma—cancer‐associated fibroblasts, immune cells and vascular cells—and how this influences their interactions with the tumor cells. Insights into the roles of Notch in cells of the tumor environment and the impact on tumor‐stroma interactions will lead to a deeper understanding of Notch signaling in cancer and inspire new strategies for Notch‐based tumor therapy.
KW - Notch signaling
KW - cancer
KW - oncogene
KW - tumor
KW - tumor microenvironment
KW - tumor suppressor gene
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U2 - 10.3390/ijms23116241
DO - 10.3390/ijms23116241
M3 - Review article
C2 - 35682918
AN - SCOPUS:85131157737
SN - 1661-6596
VL - 23
JO - International journal of molecular sciences
JF - International journal of molecular sciences
IS - 11
M1 - 6241
ER -