Lymphatic malformations: mechanistic insights and evolving therapeutic frontiers

M Petkova, I Ferby, T Mäkinen - The Journal of Clinical …, 2024 - Am Soc Clin Investig
The lymphatic vascular system is gaining recognition for its multifaceted role and broad
pathological significance. Once perceived as a mere conduit for interstitial fluid and immune …

New prospectives on treatment opportunities in RASopathies

BD Gelb, ME Yohe, C Wolf… - American Journal of …, 2022 - Wiley Online Library
The RASopathies are a group of clinically defined developmental syndromes caused by
germline variants of the RAS/mitogen‐activated protein (MAPK) cascade. The prototypic …

Microphysiological model of PIK3CA-driven vascular malformations reveals a role of dysregulated Rac1 and mTORC1/2 in lesion formation

WY Aw, C Cho, H Wang, AH Cooper, EL Doherty… - Science …, 2023 - science.org
Somatic activating mutations of PIK3CA are associated with development of vascular
malformations (VMs). Here, we describe a microfluidic model of PIK3CA-driven VMs …

Force-mediated recruitment and reprogramming of healthy endothelial cells drive vascular lesion growth

A Shapeti, J Barrasa-Fano, AR Abdel Fattah… - Nature …, 2024 - nature.com
Force-driven cellular interactions are crucial for cancer cell invasion but remain
underexplored in vascular abnormalities. Cerebral cavernous malformations (CCM), a …

PI3K-C2β limits mTORC1 signaling and angiogenic growth

P Kobialka, J Llena, N Deleyto-Seldas… - Science …, 2023 - science.org
Phosphoinositide 3-kinases (PI3Ks) phosphorylate intracellular inositol lipids to regulate
signaling and intracellular vesicular trafficking. Mammals have eight PI3K isoforms, of which …

PIK3CA-Related Disorders: From Disease Mechanism to Evidence-Based Treatments

GM Morin, L Zerbib, S Kaltenbach… - Annual Review of …, 2024 - annualreviews.org
Recent advances in genetic sequencing are transforming our approach to rare-disease
care. Initially identified in cancer, gain-of-function mutations of the PIK3CA gene are also …

Familial CCM genes might not be main drivers for Pathogenesis of sporadic CCMs-Genetic similarity between cancers and vascular malformations

J Zhang, J Croft, A Le - Journal of Personalized Medicine, 2023 - mdpi.com
Cerebral cavernous malformations (CCMs) are abnormally dilated intracranial capillaries
that form cerebrovascular lesions with a high risk of hemorrhagic stroke. Recently, several …

When, where and which PIK3CA mutations are pathogenic in congenital disorders

A Angulo-Urarte, M Graupera - Nature Cardiovascular Research, 2022 - nature.com
PIK3CA encodes the class I PI3Kα isoform and is frequently mutated in cancer. Activating
mutations in PIK3CA also cause a range of congenital disorders featuring asymmetric tissue …

Vascular malformations: An overview of their molecular pathways, detection of mutational profiles and subsequent targets for drug therapy

A Mansur, I Radovanovic - Frontiers in Neurology, 2023 - frontiersin.org
Vascular malformations are anomalies in vascular development that portend a significant
risk of hemorrhage, morbidity and mortality. Conventional treatments with surgery …

[HTML][HTML] Characterization of patient-Derived GNAQ mutated endothelial cells from capillary malformations

GB Langbroek, MLE Stor, V Janssen, A de Haan… - Journal of Investigative …, 2024 - Elsevier
Capillary malformations (CM)(port-wine stains) are congenital skin lesions that are
characterized by dilated capillaries and postcapillary venules. CMs are caused by altered …