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DDAH1 and DDAH2 drive vasculogenic mimicry and more aggressive phenotypes in triple negative breast cancer cells

Identification

Public canonical key
radar:r-218bb2cd9e450bea3c47d576bbfaccca
Authors
Jai Meyers · Lashika Weerakoon · Vinitha N. Ragavan · Natalia Jarzebska · Roman N Rodionov · Arduino Aleksander Mangoni · Julie-Ann Hulin · Sara Tommasi
Reported year
2026
Reported language
en
Source type
article
First detected
2026-11-13T12:42:57.722431+00:00
Last metadata observation
2026-11-13T12:42:57.722431+00:00
Last HTTP verification
Not checked

Institutions reported by the source

Flinders University · Technische Universität Dresden · Flinders Medical Centre

Reported affiliation countries

AU · DE

Documentary abstract — original language

The overexpression of dimethylarginine dimethylaminohydrolase 1 (DDAH1) and 2 (DDAH2) has been associated with several types of cancer. Specifically, DDAH1 has been shown to play a critical role in the establishment of a vascular network by tumour cells, vasculogenic mimicry (VM), in triple negative breast cancer (TNBC). In turn, VM favours TNBC progression and is associated with poor patient prognosis. DDAH1 is well characterised in its capacity to metabolise asymmetric dimethylarginine (ADMA), an endogenous nitric oxide synthase inhibitor. By contrast, DDAH2 is incapable of metabolising ADMA, and its ADMA-independent functions and role in TNBC are unknown. In an in vitro MDA-MB-231 TNBC cell model, CRISPR-Cas9 knockout and siRNA knockdown of either DDAH1 or DDAH2 significantly reduced VM. This effect was accompanied by a significant reduction in proliferation, migration, invasion, and Vascular endothelial growth factor A (VEGF-A) secretion. These results suggest ADMA-independent mechanisms for DDAH2 in the occurrence of VM and identify DDAH2 as a novel therapeutic target in TNBC.

Identifiers

OPENALEX
https://openalex.org/W7167971051
DOI
10.1016/j.biopha.2026.119759
PMID
https://pubmed.ncbi.nlm.nih.gov/42430838

Documentary context

Documentary family
article
Source-reported types
article
Publishers
Elsevier BV

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Sources

OpenAlex · Record 1

Cite this reference

Jai Meyers; Lashika Weerakoon; Vinitha N. Ragavan; Natalia Jarzebska; Roman N Rodionov; Arduino Aleksander Mangoni; Julie-Ann Hulin; Sara Tommasi. DDAH1 and DDAH2 drive vasculogenic mimicry and more aggressive phenotypes in triple negative breast cancer cells. 2026. https://doi.org/10.1016/j.biopha.2026.119759

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APA
Jai Meyers; Lashika Weerakoon; Vinitha N. Ragavan; Natalia Jarzebska; Roman N Rodionov; Arduino Aleksander Mangoni; Julie-Ann Hulin; Sara Tommasi. (2026). DDAH1 and DDAH2 drive vasculogenic mimicry and more aggressive phenotypes in triple negative breast cancer cells. https://doi.org/10.1016/j.biopha.2026.119759
Chicago
Jai Meyers; Lashika Weerakoon; Vinitha N. Ragavan; Natalia Jarzebska; Roman N Rodionov; Arduino Aleksander Mangoni; Julie-Ann Hulin; Sara Tommasi. DDAH1 and DDAH2 drive vasculogenic mimicry and more aggressive phenotypes in triple negative breast cancer cells. 2026. https://doi.org/10.1016/j.biopha.2026.119759
ISO 690
Jai Meyers; Lashika Weerakoon; Vinitha N. Ragavan; Natalia Jarzebska; Roman N Rodionov; Arduino Aleksander Mangoni; Julie-Ann Hulin; Sara Tommasi. DDAH1 and DDAH2 drive vasculogenic mimicry and more aggressive phenotypes in triple negative breast cancer cells. 2026. https://doi.org/10.1016/j.biopha.2026.119759

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UDTR Global Rights of Nature Legal Library. DDAH1 and DDAH2 drive vasculogenic mimicry and more aggressive phenotypes in triple negative breast cancer cells. Documentary record: https://www.declarationuniverselledesdroitsdelarbre.org/global-rights-of-nature-radar/reference/r-218bb2cd9e450bea3c47d576bbfaccca/ · Last HTTP verification: not performed

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Source roles

Bibliographic / original publication source · https://doi.org/10.1016/j.biopha.2026.119759

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