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The role of endothelial Dll4 in cancer metastasis
Publication . Dias, Liliana Mendonça da Silva; Duarte, António Freitas; Trindade, Alexandre Neto
The metastatic spread of cancer is still the major barrier to the treatment of this disease.
Cancer-mortality is mainly due to recurrence and metastasis. Although much has been
done in the field of cancer treatment, prevention and approach to metastases are still areas
not fully explored.
Over and under-expression of Dll4/Notch signaling has been demonstrated to impair tumor
growth through opposing patterns of vascular modulation in different mouse tumor models
and human cancer xenografts. Recent evidence implicates Dll4/Notch pathway in the
metastasis mechanism, but less is known about the specific role of endothelial Dll4. For this
reason, we proposed to investigate how endothelial Dll4 expression interferes with the
metastatic process. To address it we used a spontaneous metastasis mouse model based
on Lewis Lung Carcinoma (LLC) subcutaneous transplants in endothelial-specific Dll4 lossof-
function (eDll4cKO) and endothelial-specific Dll4 over-expression (D4OE) mice.
Results demonstrated that eDll4cKO is responsible for the vascular function regression that
leads to tumor growth reduction. Early steps of epithelial-to-mesenchymal transition (EMT)
and cancer stem cell selection were also inhibited by eDll4cKO, leading to a substantial
reduction of circulating tumor cells and reduction in the number and burden of macrometastases.
Intravasation and extravasation were also compromised by eDll4cKO, possibly
due to blockade of the metastatic niche.
In the case of the D4OE mice we observed that tumor growth reduction was achieved by
vessel proliferation restriction along with an improved vascular maturation, which allowed a
more efficient delivery of chemotherapy. This last effect of vessel normalization seemed to
prevent metastasis formation even though EMT markers were increased.
In conclusion, despite the opposite vascular architecture phenotypes of eDll4cKO and
D4OE, both lead to a reduction in metastasis. This is in line with the concept of Dll4 dosage
observed in the wound-healing context and represents a promising therapeutic approach in
metastasis prevention/ treatment.
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Fundação para a Ciência e a Tecnologia
Programa de financiamento
SFRH
Número da atribuição
SFRH/BD/74229/2010
