Publications by authors named "Karen Strathdee"

Background: Glioblastomas have highly infiltrative growth patterns that contribute to recurrence and poor survival. Despite infiltration being a critical therapeutic target, no clinically useful therapies exist that counter glioblastoma invasion. Here, we report that inhibition of ataxia telangiectasia and Rad 3 related kinase (ATR) reduces invasion of glioblastoma cells through dysregulation of cytoskeletal networks and subsequent integrin trafficking.

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Glioblastoma (GBM) is the most prevalent malignant primary brain tumour in adults. GBM typically has a poor prognosis, mainly due to a lack of effective treatment options leading to tumour persistence or recurrence. We investigated the therapeutic potential of targeting anti-apoptotic BCL-2 proteins in GBM.

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Purpose: Low-dose whole lung radiation therapy (LDLR) has been proposed as a treatment for patients with acute respiratory distress syndrome associated with SARS-CoV-2 infection, and clinical trials are underway. There is an urgent need for preclinical evidence to justify this approach and inform dose, scheduling, and mechanisms of action.

Methods And Materials: Female C57BL/6 mice were treated with intranasal bleomycin sulfate (7.

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Article Synopsis
  • - The OPARATIC trial investigated how well the PARP inhibitor olaparib penetrates recurrent glioblastoma tumors and its safety when combined with low-dose TMZ chemotherapy.
  • - Preclinical studies showed that olaparib did not penetrate the brain well in rats but was successfully found in human tumor samples, with 36% of patients remaining progression-free at six months after treatment.
  • - While olaparib was effective at radiosensitizing glioblastoma cells, it also increased the hematological side effects of TMZ, leading to a recommended dose regimen of olaparib (150 mg) three times a week alongside TMZ (75 mg/m² daily) for 42 days.
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Glioblastoma (GBM) is an aggressive and incurable primary brain tumor that causes severe neurologic, cognitive, and psychologic symptoms. Symptoms are caused and exacerbated by the infiltrative properties of GBM cells, which enable them to pervade the healthy brain and disrupt normal function. Recent research has indicated that although radiotherapy (RT) remains the most effective component of multimodality therapy for patients with GBM, it can provoke a more infiltrative phenotype in GBM cells that survive treatment.

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Article Synopsis
  • Glioblastoma (GBM) is a deadly brain tumor known for its treatment resistance, largely due to cancer stem-like cells (GSC) that promote tumor growth and recurrence.
  • The study identifies that high levels of DNA replication stress (RS) in GSC lead to increased radiation resistance, a major barrier in treating GBM.
  • By targeting RS with a combination of ATR and PARP inhibitors, researchers demonstrated a specific cytotoxic effect on GSC, suggesting a new therapeutic approach that could improve treatment efficacy in GBM.
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Resistance to radiotherapy in glioblastoma (GBM) is an important clinical problem and several authors have attributed this to a subpopulation of GBM cancer stem cells (CSCs) which may be responsible for tumour recurrence following treatment. It is hypothesised that GBM CSCs exhibit upregulated DNA damage responses and are resistant to radiation but the current literature is conflicting. We investigated radioresistance of primary GBM cells grown in stem cell conditions (CSC) compared to paired differentiated tumour cell populations and explored the radiosensitising effects of the ATM inhibitor KU-55933.

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Background: Enteroendocrine cells populate gastrointestinal tissues and are known to translate local cues into systemic responses through the release of hormones into the bloodstream.

Results: Here we report a novel function of enteroendocrine cells acting as local regulators of intestinal stem cell (ISC) proliferation through modulation of the mesenchymal stem cell niche in the Drosophila midgut. This paracrine signaling acts to constrain ISC proliferation within the epithelial compartment.

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High tumor burden is associated with increased levels of circulating inflammatory cytokines that influence the pathophysiology of the tumor and its environment. The cellular and molecular events mediating the organismal response to a growing tumor are poorly understood. Here, we report a bidirectional crosstalk between epithelial tumors and the fat body-a peripheral immune tissue-in Drosophila.

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Objective: Colorectal cancer (CRC) is a major contributor to cancer mortality and morbidity. LIM kinase 2 (LIMK2) promotes tumour cell invasion and metastasis. The objectives of this study were to determine how LIMK2 expression is associated with CRC progression and patient outcome, and to use genetically modified Drosophila and mice to determine how LIMK2 deletion affects gastrointestinal stem cell regulation and tumour development.

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Article Synopsis
  • In cancer, inflammatory signals called cytokines can have both good and bad effects, and this is especially true for a cytokine called TNF.
  • A study using fruit flies showed that TNF can help get rid of certain cancer cells, but in some cases, it actually helps tumors grow instead.
  • The research also found that a specific cancer mutation (Ras) can trick TNF into promoting tumor growth, which makes the cancer more dangerous and harmful to the organism.
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Understanding how cognitive processes including learning, memory, decision making and ideation are encoded by the genome is a key question in biology. Identification of sets of genes underlying human mental disorders is a path towards this objective. Schizophrenia is a common disease with cognitive symptoms, high heritability and complex genetics.

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