GROUP CIB-ECS

Ana O’Loghlen obtained her BSc in Biology and her PhD in Biomedicine from the University Complutense of Madrid (Spain). Her work focused on unveiling the role of the novel MAP kinases- termed Mnks- in the context of brain ischemia. She obtained more than 5 first author publications from her PhD. She was also a visiting scientist at the University of Dundee under the supervision of Dr Christpher Proud.

After her PhD, she was recruited to the Spanish National Cancer Research Centre (CNIO) under the supervision of Dr Angel Nebreda. She later moved to Imperial College London (UK) to work in Dr Jesus Gil´s lab where her work focused on understanding the cellular phenotype senescence. During this period, she performed several functional screens to identify novel regulators of senescence, where she identified immune cell regulators (Cell 2008, Cell Cycle 2008), microRNAs (Cell Stem Cell 2012, Ageing Cell 2015) and epigenetic regulators (EMBO J 2013,Trends Cell Biol 2014, Oncogene 2015). After a brief period at the former London Research Centre (Francis Crick Institute) with Gordon Peter she was recruited as a group leader in Queen Mary University London (UK). Since then, her lab continues to unveil the basic mechanisms regulating senescence and its influence within its microenvironment. Our latest work has identified additional novel regulators of senescence such as integrin beta 3 subunit, ITGB3 (Cell Reports 2017). In addition, we found a role for the interferon (IFITM3) and glutathione (GSTM2) pathways in senescence and ageing via intercellular communication through extracellular vesicles (Cell Reports 2019, Cell Metabolism 2020, Trends Cell Biol 2020, Ageing Cell 2021). More recently, by performing a genome-wide CRISPR/Cas9 screen we have identified two genes implicated in the coagulation pathway – the coagulation factor IX (F9) and Protein Z Vitamin K Dependent Plasma Glycoprotein (PROZ) – whose loss prevent the induction of senescence. We believe these markers could be used to predict patient response to CDK4/6 inhibitors improving the efficacy of cancer treatments and overall disease outcome (Cell Death Dis 2022).

The O’Loghlen lab is committed to the training of scientists with different levels of expertise. Associated to the SenesceX project is a PhD student, an MSc student and a lab technician who carries her own lab project.

The CIB has all the necessary infrastructure for the development of this project, from cell culture facilities, to animal housing services, imaging and holds an excellent electron microscopy facility.

PROJECTS (LAST 5 YEARS)

  • 2023–2025 – Agencia Estatal de Investigación. PI: Dr O’Loghlen. €200,000.
    “Estudiando la heterogeneidad y dinámica del secretoma senescente en el envejecimiento”.
    Referencia: CNS2022-135134. Afiliación: CIB.

  • 2022–2026 – Comunidad de Madrid (Consorcio). Co-PI: Dr O’Loghlen. €828,000.
    “Senescencia celular en fisiología y enfermedad”.
    Referencia: P2022/BMD-7393. Afiliación: CIB.

  • 2022–2026 – Agencia Estatal de Investigación. PI: Dr O’Loghlen. €200,000.
    “Investigación de los cambios metabolómicos producidos por vesículas extracelulares durante el envejecimiento”.
    Referencia: PID2021-125656OB-I00. Afiliación: CIB.

  • 2020–2022 – Barts Charity London. PI: Dr O’Loghlen. £320,000.
    “The potential of extracellular vesicles as a therapeutic approach to prevent ageing”.
    Referencias: MGU0497, G002158. Afiliación: Queen Mary, UK.

  • 2020–2021 – StarkAge Therapeutics (Industria). PI: Dr O’Loghlen. £96,000.
    “Extracellular vesicles in lung fibrosis”.
    Afiliación: Queen Mary, UK.

THESIS  (LAST 5 YEARS)

  • 2025 – Antonio Merino. PI: Dr O’Loghlen. Contrato SenesceX-CM (2022).
  • 2025 – Ana Mariscal. PI: Dr O’Loghlen. Beca Fundación Ramón Areces.
  • 2023 – Marta Menéndez. PI: Dr O’Loghlen. Beca Comunidad de Madrid.
  • 2023 – Lewis Woodward. Co-PI: Dr O’Loghlen. Rosetrees Foundation Fellowship.

MERITS & RESPONSIBILITIES

  • Miembro del comité de evaluación de proyectos de la Agencia Estatal de Francia (ANR) (2022–2025).
  • Miembro del comité asesor científico externo de StarkAge Therapeutics (2022).
  • Tesorera de la International Cellular Senescence Association (ICSA) (2023–actualidad).
  • Tesorera de la Sociedad Española de Senescencia (SENESCEL) (2023–2025).
  • Directora de la comisión de seminarios del Departamento de Biomedicina en Londres (2015–2016) y en el CIB/CSIC (2022–2025).
  • Revisora para revistas científicas de alto impacto, entre ellas Nature Metabolism, Cell Metabolism, Nature Aging y Nature Cell Biology.
  • Evaluadora de proyectos para agencias nacionales e internacionales en Europa, Estados Unidos, Sudamérica y Asia.

RELEVANT PUBLICATIONS

  • 2026 – Mira-Carnicer M, Menendez-Garcia M, Merino-Navarro A, Palomino-Lozano C, Anton-Barros C, Palmero I, Malaspina A, Montesinos J, O’Loghlen A (2026) The resolvin D and E biogenesis pathway regulates senescence and ageing. bioRxiv 2026.01.26.701588. doi: https://doi.org/10.64898/2026.01.26.701588
  • 2025 – Menéndez-García M, Merino-Navarro A, O’Loghlen A (2025) p16INK4A expression induces paracrine senescence via small extracellular vesicles. bioRxiv 2025.12.09.689258. doi: https://doi.org/10.64898/2025.12.09.689258
  • 2025 – James EN, Teh MT, Li Y, Wagner-Bock C, Al-Khateeb ZF, Karen-Ng LP, Roberts T, Synchyshyn L, Lewis A, O’Loghlen A, Silver A, Michael-Titus AT, Bennett M, Bundy JG, Mycielska ME, Parkinson EK (2025) Membrane transporter progressive ankylosis protein homologue (ANKH/Ank) partially mediates senescence-derived extracellular citrate and is regulated by DNA damage, inflammation, and ageing. Front Aging. 6:1583288. doi: 10.3389/fragi.2025.1583288
  • 2024 – O’Loghlen A (2024) IL-11 as a master regulator of ageing. Nat Rev Mol Cell Biol. doi: 10.1038/s41580-024-00793-1
  • 2024 – Aleman M et al. (2024) Coagulation and platelet biology at the intersection of health and disease: illustrated capsules of the 11th Symposium on Hemostasis at the University of North Carolina. Res Pract Thromb Haemost. 8(3):102395. doi: 10.1016/j.rpth.2024.102395
  • 2024 – Welsh et al. (2024) Minimal information for studies of extracellular vesicles (MISEV2023): From basic to advanced approaches. J Extracell Vesicles. 13(2):e12404. doi: 10.1002/jev2.12404
  • 2022 – Mylonas A, O’Loghlen A (2022) Cellular Senescence and Ageing: mechanisms and interventions. Frontiers in Aging. 3:866718
  • 2022 – O’Loghlen A (2022) The potential of aging rejuvenation. Cell Cycle. 21(2):111-116
  • 2022 – Carpintero-Fernández P, Borghesan M, Eleftheriadou O, Fafián-Labora JA, Mitchell TP, Nightingale TD, Mayán MD, O’Loghlen A (2022) The coagulation factor IX (F9) loss of function prevents the cell cycle arrest induced by CDK4/6 inhibitors treatment. Cell Death and Disease. 13(2):163
  • 2021 – Fafián-Labora JA, O’Loghlen A (2021) NF-kB/IKK activation by small extracellular vesicles within the SASP. Aging Cell. 20(7):e13426
  • 2021 – Guerrini L, Garcia-Rico E, O’Loghlen A, Giannini V, Alvarez-Puebla RA (2021) Surface-Enhanced Raman Scattering (SERS) Spectroscopy for Sensing and Characterization of Exosomes in Cancer Diagnosis. Cancers. 13(9):2179
  • 2021 – Prasanna PG et al. (2021) Therapy-Induced Senescence: Opportunities to Improve Anti-Cancer Therapy. J Natl Cancer Inst. 113(10):1285-1298
  • 2020 – Fafián-Labora JA, Rodríguez-Navarro JA, O’Loghlen A (2020) Small Extracellular Vesicles Have GST Activity and Ameliorate Senescence-Related Tissue Damage. Cell Metabolism. 32:71-86.e5
  • 2020 – Fafián-Labora JA, O’Loghlen A (2020) Classical and Nonclassical Intercellular Communication in Senescence and Ageing. Trends in Cell Biology. 30:628-639
  • 2019 – Borghesan M et al. (2019) Small Extracellular Vesicles Are Key Regulators of Non-cell Autonomous Intercellular Communication in Senescence via the Interferon Protein IFITM3. Cell Reports. 27:3956-3971.e6
  • 2017 – Rapisarda V et al. (2017) Integrin Beta 3 Regulates Cellular Senescence by Activating the TGF-β Pathway. Cell Reports. 18:2480-2493
  • 2008 – Acosta JC et al. (2008) Chemokine Signaling via the CXCR2 Receptor Reinforces Senescence. Cell. 133:1006-1018

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