Filter By:

Journal Check one or more journals to show results from those journals only.

Choose more journals

Article type Check one or more article types to show results from those article types only.
Subject Check one or more subjects to show results from those subjects only.
Date Choose a date option to show results from those dates only.

Custom date range

Clear all filters
Sort by:
Showing 1–7 of 7 results
Advanced filters: Author: Sunil J Advani Clear advanced filters
  • Tumors hijack cellular pathways to evade the effects of cancer therapy. Here, Advaniet al. show that DNA damage-induced phosphorylation of CRAF Serine 338 triggers DNA repair by recruiting CHK2, highlighting a role for CRAF independent from its canonical function as a kinase.

    • Sunil J. Advani
    • Maria Fernanda Camargo
    • David A. Cheresh
    ResearchOpen Access
    Nature Communications
    Volume: 6, P: 1-8
  • Raf kinase activity is deregulated in cancers and is thought to promote tumor growth by inducing proliferation signaling through MEK/Erk. This report identifies a new role for c-Raf independent of MEK/Erk and relying on phosphorylation of Ser338. Phospho–C-Raf interacts with the mitotic kinases Aurora-A and Plk1, activating the latter to promote mitotic progression and increase cell division, and this pathway is a crucial mediator for the protumorigenic effect of c-Raf in vivo.

    • Ainhoa Mielgo
    • Laetitia Seguin
    • David A Cheresh
    Research
    Nature Medicine
    Volume: 17, P: 1641-1645
  • Monomethyl auristatin (MMAE), also known for its radiosensitizer properties, is a common antibody drug conjugate used for cancer therapy. Here the authors show that, in combination with radiotherapy, tumor-directed antibodies or peptides conjugated to MMAE promote anti-tumor immune responses, improving response to checkpoint inhibitors in preclinical cancer models.

    • Dina V. Hingorani
    • Michael M. Allevato
    • Sunil J. Advani
    ResearchOpen Access
    Nature Communications
    Volume: 13, P: 1-16
  • The tumour microenvironment can be modulated to sensitize tumours to the effects of therapy. Here the authors show that radiation induced miR-103 downregulates TREX1 in endothelial cells, decreases angiogenesis and leads to the secretion of proinflammatory mediators that reduce tumour growth.

    • RaeAnna Wilson
    • Cristina Espinosa-Diez
    • Sudarshan Anand
    ResearchOpen Access
    Nature Communications
    Volume: 7, P: 1-10
  • Drugs that sensitize tumour cells to ionizing radiation are prized because they can overcome resistance to radiotherapy. Here, the authors show that anti-tubulin drugs conjugated to cetuximab or trastuzumab can radiosensitize EGFR- or HER2-expressing tumors by increasing DNA damage and cell death due to ionizing radiation.

    • Stephen R. Adams
    • Howard C. Yang
    • Sunil J. Advani
    ResearchOpen Access
    Nature Communications
    Volume: 7, P: 1-11
  • Dexamethasone has been shown to have survival benefits for critically ill patients hospitalised with COVID-19 in the UK. Here, the authors estimated the number of lives that could be saved through a UK and global roll out of the drug and demonstrate that it is a cost-effective option.

    • Ricardo Águas
    • Adam Mahdi
    • Mesulame Namedre
    ResearchOpen Access
    Nature Communications
    Volume: 12, P: 1-8