TY - JOUR
T1 - Interactions of Melanoma Cells with Distal Keratinocytes Trigger Metastasis via Notch Signaling Inhibition of MITF
AU - Golan, Tamar
AU - Messer, Arielle R.
AU - Amitai-Lange, Aya
AU - Melamed, Ze'ev
AU - Ohana, Reut
AU - Bell, Rachel E.
AU - Kapitansky, Oxana
AU - Lerman, Galya
AU - Greenberger, Shoshana
AU - Khaled, Mehdi
AU - Amar, Nira
AU - Albrengues, Jean
AU - Gaggioli, Cedric
AU - Gonen, Pinchas
AU - Tabach, Yuval
AU - Sprinzak, David
AU - Shalom-Feuerstein, Ruby
AU - Levy, Carmit
N1 - Publisher Copyright:
© 2015 Elsevier Inc.
PY - 2015/8/20
Y1 - 2015/8/20
N2 - The most critical stage in initiation of melanoma metastasis is the radial to vertical growth transition, yet the triggers of this transition remain elusive. We suggest that the microenvironment drives melanoma metastasis independently of mutation acquisition. Here we examined the changes in microenvironment that occur during melanoma radial growth. We show that direct contact of melanoma cells with the remote epidermal layer triggers vertical invasion via Notch signaling activation, the latter serving to inhibit MITF function. Briefly, within the native Notch ligand-free microenvironment, MITF, the melanocyte lineage master regulator, binds and represses miR-222/221 promoter in an RBPJK-dependent manner. However, when radial growth brings melanoma cells into contact with distal differentiated keratinocytes that express Notch ligands, the activated Notch intracellular domain impairs MITF binding to miR-222/221 promoter. This de-repression of miR-222/221 expression triggers initiation of invasion. Our findings may direct melanoma prevention opportunities via targeting specific microenvironments.
AB - The most critical stage in initiation of melanoma metastasis is the radial to vertical growth transition, yet the triggers of this transition remain elusive. We suggest that the microenvironment drives melanoma metastasis independently of mutation acquisition. Here we examined the changes in microenvironment that occur during melanoma radial growth. We show that direct contact of melanoma cells with the remote epidermal layer triggers vertical invasion via Notch signaling activation, the latter serving to inhibit MITF function. Briefly, within the native Notch ligand-free microenvironment, MITF, the melanocyte lineage master regulator, binds and represses miR-222/221 promoter in an RBPJK-dependent manner. However, when radial growth brings melanoma cells into contact with distal differentiated keratinocytes that express Notch ligands, the activated Notch intracellular domain impairs MITF binding to miR-222/221 promoter. This de-repression of miR-222/221 expression triggers initiation of invasion. Our findings may direct melanoma prevention opportunities via targeting specific microenvironments.
UR - http://www.scopus.com/inward/record.url?scp=84939575032&partnerID=8YFLogxK
U2 - 10.1016/j.molcel.2015.06.028
DO - 10.1016/j.molcel.2015.06.028
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C2 - 26236014
AN - SCOPUS:84939575032
SN - 1097-2765
VL - 59
SP - 664
EP - 676
JO - Molecular Cell
JF - Molecular Cell
IS - 4
ER -