Tuomas Sipilä

ORCID: 0000-0002-9551-8042
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About
Contact & Profiles
Research Areas
  • Angiogenesis and VEGF in Cancer
  • Lipid metabolism and disorders
  • Glaucoma and retinal disorders
  • Retinal Diseases and Treatments
  • Cell Adhesion Molecules Research
  • Lymphatic System and Diseases
  • Bioinformatics and Genomic Networks
  • Lipid metabolism and biosynthesis
  • Proteoglycans and glycosaminoglycans research
  • Hippo pathway signaling and YAP/TAZ
  • Lipid Membrane Structure and Behavior
  • Kruppel-like factors research
  • Diabetes, Cardiovascular Risks, and Lipoproteins
  • Genetic Associations and Epidemiology
  • Acute Myeloid Leukemia Research
  • Nanoparticle-Based Drug Delivery
  • RNA Interference and Gene Delivery
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Retinal Development and Disorders
  • Genetic Mapping and Diversity in Plants and Animals
  • Cancer-related molecular mechanisms research
  • Coagulation, Bradykinin, Polyphosphates, and Angioedema

Institute for Molecular Medicine Finland
2019-2021

University of Helsinki
2010-2021

Wihuri Research Institute
2016-2020

Angiopoietins regulate vascular homeostasis via the endothelial Tie receptor tyrosine kinases. Angiopoietin-1 (Ang1) supports stabilization Tie2 activation. Angiopoietin-2 (Ang2) functions as a context-dependent agonist/antagonist promoting pathological angiogenesis, permeability and inflammation. Elucidating Ang2-dependent mechanisms of destablization is critical for rational design angiopoietin antagonists that have demonstrated therapeutic efficacy in cancer trials. Here, we report Ang2,...

10.1038/ncomms6962 article EN cc-by Nature Communications 2015-01-30

The angiopoietin/Tie (ANG/Tie) receptor system controls developmental and tumor angiogenesis, inflammatory vascular remodeling, vessel leakage. ANG1 is a Tie2 agonist that promotes stabilization in inflammation sepsis, whereas ANG2 context-dependent or antagonist. A limited understanding of ANG signaling mechanisms the orphan Tie1 has hindered development ANG/Tie-targeted therapeutics. Here, we determined both binding to increases Tie1-Tie2 interactions β1 integrin-dependent manner regulates...

10.1172/jci84923 article EN Journal of Clinical Investigation 2016-08-21
Rubina Tabassum Joel Rämö Pietari Ripatti Jukka Koskela Mitja Kurki and 95 more Juha Karjalainen Priit Palta Shabbeer Hassan Javier Núñez-Fontarnau Tuomo Kiiskinen Sanni Söderlund Niina Matikainen Mathias J. Gerl Michał A. Surma Christian Klose Nathan O. Stitziel Hannele Laivuori Aki S. Havulinna Susan K. Service Veikko Salomaa Matti Pirinen Anu Jalanko Jaakko Kaprio Kati Donner Mari Kaunisto Nina Mars Alexander Dada Anastasia Shcherban Andrea Ganna Arto Lehistö Elina Kilpeläinen Georg Brein Awaisa Ghazal Jarmo Harju Kalle Pärn Pietro Della Briotta Parolo Risto Kajanne Susanna Lemmelä Timo P. Sipilä Tuomas Sipilä Ulrike Lyhs Vincent Llorens Teemu Niiranen Kati Kristiansson Lotta Männikkö Manuel González Jiménez Markus Perola Regis Wong Terhi Kilpi Tero Hiekkalinna Elina Järvensivu Essi Kaiharju Hannele Mattsson Markku Laukkanen Päivi Laiho Sini Lähteenmäki Tuuli Sistonen Sirpa Soini Adam Ziemann Anne Lehtonen Apinya Lertratanakul Bob Georgantas Bridget Riley‐Gillis Danjuma Quarless Fedik Rahimov Graham Heap Howard J. Jacob Jeffrey F. Waring J. Wade Davis Nizar Smaoui Relja Popovic Sahar Esmaeeli Jeff Waring Athena Matakidou Ben Challis David A. Close Slavé Petrovski Antti Karlsson Johanna Schleutker Kari Pulkki Petri Virolainen Lila Kallio Graham J. Mann Sami Heikkinen Veli‐Matti Kosma Chia‐Yen Chen Heiko Runz Jiang Liu Paola G. Bronson Sally John Sanni Lahdenperä Susan Eaton Wei Zhou Minna Hendolin Outi Tuovila Raimo Pakkanen Joseph Maranville Keith Usiskin Marla Hochfeld Robert Plenge

Abstract Understanding genetic architecture of plasma lipidome could provide better insights into lipid metabolism and its link to cardiovascular diseases (CVDs). Here, we perform genome-wide association analyses 141 species (n = 2,181 individuals), followed by phenome-wide scans with 25 CVD related phenotypes 511,700 individuals). We identify 35 lipid-species-associated loci (P <5 ×10 −8 ), 10 which associate risk including five new loci- COL5A1 , GLTPD2 SPTLC3 MBOAT7 GALNT16 (false...

10.1038/s41467-019-11954-8 article EN cc-by Nature Communications 2019-09-24

Primary lymphedema is caused by developmental and functional defects of the lymphatic vascular system that result in accumulation protein-rich fluid tissues, resulting edema. The 28 currently known genes causing primary can explain <30% cases. Angiopoietin 1 (ANGPT1) ANGPT2 function via TIE1-TIE2 (tyrosine kinase with immunoglobulin-like epidermal growth factor-like domains 2) receptor complex α5β1 integrin to form an endothelial cell signaling pathway critical for blood vessel formation...

10.1126/scitranslmed.aax8013 article EN Science Translational Medicine 2020-09-09
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