Publications by authors named "LEEK R"

Article Synopsis
  • - Current biomarkers for assessing the risk of tumor progression in ER-negative breast cancer patients are inadequate, prompting a study on the role of the AIPL1-NUB1 pathway in tumor suppression under hypoxic conditions.
  • - The study found that downregulation of AIPL1 leads to the deactivation of NUB1, observed through in vitro tests using breast cancer cell lines, and analysis of patient samples revealed significant differences in protein expression levels.
  • - Ultimately, lower levels of cytoplasmic NUB1 were linked to poorer overall survival rates in patients, indicating that both NUB1 and AIPL1 may play crucial roles in the prognosis of breast cancer, particularly in ER-negative cases.
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ELTD1/ADGRL4 expression is increased in the vasculature of a number of tumor types and this correlates with a good prognosis. Expression has also been reported in some tumor cells with high expression correlating with a good prognosis in hepatocellular carcinoma (HCC) and a poor prognosis in glioblastoma. Here we show that 35% of primary human breast tumors stain positively for ELTD1, with 9% having high expression that correlates with improved relapse-free survival.

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Introduction: Liver transplant (LT) recipients have limited understanding of post-transplant chronic kidney disease (CKD) despite an excellent pre-existing framework of transplant care. This pilot study examined the efficacy and feasibility of a tailored educational and goal-setting tool in improving CKD knowledge among LT recipients with early-stage CKD.

Methods: In this prospective cohort study, we administered the CKD educational and goal-setting tool to 81 LT recipients between 7/1/2016 and 12/31/2017.

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Introduction: Direct-acting antivirals (DAAs) have transformed hepatitis C virus (HCV) management post-liver transplant. As HCV clears during DAA treatment, hepatic metabolism improves, resulting in decreased tacrolimus concentrations that may require dose adjustment. The purpose of this study was to determine appropriate management of immunosuppression in liver transplant recipients during and following treatment of HCV.

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  • DLL4 and JAG1 are two important molecules in tumors that help form blood vessels, but they act in opposite ways in mice.
  • Both of these molecules make tumor blood vessels grow, but DLL4 makes fewer, larger vessels while JAG1 makes more, smaller vessels.
  • Targeting DLL4 and JAG1 together may be an effective way to treat tumors by stopping them from growing and improving blood flow in the tumors.
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Background: Hypoxia imaging is a promising tool for targeted therapy but the links between imaging features and underlying molecular characteristics of the tumour have not been investigated. The aim of this study was to compare hypoxia biomarkers and gene expression in oropharyngeal squamous cell carcinoma (OPSCC) diagnostic biopsies with hypoxia imaged with Cu-ATSM PET/CT.

Methods: Cu-ATSM imaging, molecular and clinical data were obtained for 15 patients.

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spp. are saprobic fungi that cause serious infections in immunocompromised hosts and in near-drowning victims. Solid organ transplant recipients are at increased risk of scedosporiosis as they require aggressive immunosuppression to prevent allograft rejection.

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Background: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease resulting in death, usually from respiratory failure, within 2-3 years of symptom onset. Non-invasive ventilation (NIV) is a treatment that when given to patients in respiratory failure leads to improved survival and quality of life. Diaphragm pacing (DP), using the NeuRx/4(®) diaphragm pacing system (DPS)™ (Synapse Biomedical, Oberlin, OH, USA), is a new technique that may offer additional or alternative benefits to patients with ALS who are in respiratory failure.

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Regions of hypoxia in tumours can be modelled in vitro in 2D cell cultures with a hypoxic chamber or incubator in which oxygen levels can be regulated. Although this system is useful in many respects, it disregards the additional physiological gradients of the hypoxic microenvironment, which result in reduced nutrients and more acidic pH. Another approach to hypoxia modelling is to use three-dimensional spheroid cultures.

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Background: Angiogenesis is not essential for tumours to develop and expand, as cancer can also grow in a non-angiogenic fashion, but why this type of growth occurs is unknown. Surprisingly, our data from mRNA transcription profiling did not show any differences in the classical angiogenic pathways, but differences were observed in mitochondrial metabolic pathways, suggesting a key role for metabolic reprogramming. We then validated these results with mRNA profiling by investigating differential protein expression via immunohistochemistry in angiogenic and non-angiogenic non-small cell lung cancers (NSCLCs).

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Cancer-associated fibroblasts (CAFs) play a key role in promoting tumor growth, acting through complex paracrine regulation. GTP cyclohydrolase (GTPCH) expression for tetrahydrobiopterin synthesis in tumor stroma is implicated in angiogenesis and tumor development. However, the clinical significance of GTPCH expression in breast cancer is still elusive and how GTPCH regulates stromal fibroblast and tumor cell communication remains unknown.

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Purpose: Enoticumab (REGN421) is a fully human IgG1 monoclonal antibody that binds human Dll4 and disrupts Notch-mediated signaling. The main objectives of this trial were to determine the safety, dose-limiting toxicities (DLT), pharmacokinetics (PK), and recommended phase II dose (RP2D) of enoticumab.

Experimental Design: Enoticumab was administered intravenously, with dose escalations from 0.

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This study was undertaken to investigate the associations of blood vessel invasion (BVI), lymphatic vessel invasion (LVI) or other variables and long-term survival in 173 Japanese and 184 British patients with primary invasive breast cancer, and whether they are associated with survival differences between Japanese and British patients. BVI was detected by objective methods, using both factor VIII-related antigen (F-VIII) staining and elastica van Gieson (E v G) staining. BVI was classified into three subtypes.

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Article Synopsis
  • JMY is a protein that binds to p300 and has a dual role: it helps enhance P53 transcription to respond to DNA damage and promotes cell movement by aiding actin filament assembly in the cytoplasm.
  • Its function can vary, potentially acting as a tumor suppressor or an oncogene depending on the environment within the cell.
  • Research using a monoclonal antibody against JMY showed variable expression in normal and cancerous tissues, suggesting it may suppress tumor growth in some cases while promoting metastasis in others.
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  • Trastuzumab improves survival for HER2 positive breast cancer patients, but resistance to treatment remains a significant issue, potentially linked to the protein ADAM17 and the other protease ADAM10.
  • In experiments, trastuzumab increased ADAM10 expression in cancer cell lines and mouse models, which was associated with reduced protein kinase B (PKB) phosphorylation and hindered treatment responses.
  • Inhibition of ADAM10 led to better responses to trastuzumab in both naive and resistant cancer cells, and higher ADAM10 levels in patients were linked to poorer treatment outcomes and relapse-free survival, suggesting ADAM10 could serve as a therapeutic target and biomarker.
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Background: The lipogenic transcription factor carbohydrate response element-binding protein (ChREBP) may play a key role in malignant progression of breast cancer by allowing metabolic adaptations to take place in response to changes in oxygenation.

Methods: Immunohistochemical analysis of ChREBP was carried out in human breast tumour tissue microarrays representative of malignant progression from normal breast through to metastatic cancer. The ChREBP protein and mRNA expressions were then analysed in a series of breast cancers for correlative analysis with common and breast-specific hypoxia signatures, and survival.

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  • The study investigates the role of calcitonin receptor-like receptor (CLR) and its ligand adrenomedullin (ADM) in tumor angiogenesis, particularly in clear cell renal cell carcinoma (RCC).
  • Researchers performed gene expression profiling and immunohistochemistry on various tumors to assess ADM and CLR levels, finding significant upregulation in RCC compared to normal tissue.
  • The findings indicate that higher CLR expression in RCC correlates with advanced tumor stages and poorer overall survival, suggesting the potential for CLR as a therapeutic target in future cancer treatment strategies.
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  • Scientists found that using a drug called bevacizumab helps patients with a type of brain cancer called glioblastoma respond better to chemotherapy and live longer without the cancer getting worse.
  • However, tumors often adapt and resist the treatment, so researchers are exploring other drugs that can work well with bevacizumab to stop this resistance.
  • In their study, they discovered that combining bevacizumab with another drug called dichloroacetate (DCA) worked much better together than using either one alone, suggesting this combo could be a strong fight against brain cancer.
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Chemically and biologically modified nanoparticles are increasingly considered as viable and multifunctional tools to be used in cancer theranostics. Herein, we demonstrate that coordination of alizarin blue black B (ABBB) to the TiO(2) nanoparticle surface enhances the resulting nanoparticles by (1) creating distinct fluorescence emission spectra that differentiate smaller TiO(2) nanoparticles from larger TiO(2) nanoparticle aggregates (both in vitro and intracellular) and (2) enhancing visible light activation of TiO(2) nanoparticles above previously described methods to induce in vitro and intracellular damage to DNA and other targets. ABBB-TiO(2) nanoparticles are characterized through sedimentation, spectral absorbance, and gel electrophoresis.

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Hypoxia-inducible factors, HIF-1α and HIF-2α, are expressed in the majority of clear-cell renal cell carcinoma (CC-RCC). In vitro, HIFα isoforms regulate a differential set of genes, and their effects in vivo within CC-RCC tumours may affect outcome. The role of angiogenesis and HIFα transcriptional products, including those involved in cell metabolism and morphological dedifferentiation have not been extensively investigated and might have relevance to the development of antiangiogenic or anti-HIFα trials in primary CC-RCC, either before or after radical nephrectomy.

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Article Synopsis
  • Bevacizumab is a drug that helps stop the growth of blood vessels in tumors, but sometimes tumors find a way to resist it, especially when they become low in oxygen.
  • Researchers found that a gene called CAIX, which gets turned on when there's not enough oxygen, is linked to how poorly people with certain cancers do when treated with bevacizumab.
  • By lowering the CAIX gene in lab-grown cancer cells, they found that it made the tumors grow slower and helped the bevacizumab work better, suggesting targeting CAIX could be a useful addition to cancer treatments.
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Biologically and chemically modified nanoparticles are gaining much attention as a new tool in cancer detection and treatment. Herein, we demonstrate that an alizarin red S (ARS) dye coating on TiO2 nanoparticles enables visible light activation of the nanoparticles leading to degradation of neighboring biological structures through localized production of reactive oxygen species. Successful coating of nanoparticles with dye is demonstrated through sedimentation, spectrophotometry, and gel electrophoresis techniques.

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Article Synopsis
  • * Transduced glioblastoma cells expressing DLL4 displayed resistance to the VEGF-A inhibitor bevacizumab, as DLL4-Notch signaling enhanced blood supply and rendered large vessels insensitive to treatment.
  • * Targeting Notch signaling using a γ-secretase inhibitor effectively disrupted this resistance by reducing large vessels and altering multiple resistance mechanisms, highlighting potential combination therapies to improve the effectiveness of existing antiangiogenic treatments.
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Background: To investigate small-nucleolar RNAs (snoRNAs) as reference genes when measuring miRNA expression in tumour samples, given emerging evidence for their role in cancer.

Methods: Four snoRNAs, commonly used for normalisation, RNU44, RNU48, RNU43 and RNU6B, and miRNA known to be associated with pathological factors, were measured by real-time polymerase chain reaction in two patient series: 219 breast cancer and 46 head and neck squamous cell carcinoma (HNSCC). SnoRNA and miRNA were then correlated with clinicopathological features and prognosis.

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