9 results match your criteria: "Centre for Genomics and Personalised Health at the Translational Research Institute[Affiliation]"

Article Synopsis
  • - Breast cancer (BCa) presents a significant health challenge worldwide, with many tumors showing extensive genetic alterations known as somatic copy number alterations (CNAs) that influence tumor behavior and patient outcomes.
  • - Loss of the chromosome segment 13q14.2 is a common and important CNA found in up to 63% of BCa patients, associated with poorer survival rates, and its impact is complex, enhancing both cancer cell growth and immune responses in the tumor environment.
  • - This loss of 13q14.2 also increases the effectiveness of BCL2 inhibitors in treating BCa, suggesting it could be used as a biomarker to help predict patient prognosis and guide treatment options.
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Targeting the COMMD4-H2B protein complex in lung cancer.

Br J Cancer

December 2023

Queensland University of Technology (QUT), School of Biomedical Sciences, Centre for Genomics and Personalised Health at the Translational Research Institute, 37 Kent Street, Woolloongabba, QLD, 4102, Australia.

Background: Lung cancer is the biggest cause of cancer-related deaths worldwide. Non-small cell lung cancer (NSCLC) accounts for 85-90% of all lung cancers. Identification of novel therapeutic targets are required as drug resistance impairs chemotherapy effectiveness.

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Stochastic epithelial-mesenchymal transitions diversify non-cancerous lung cell behaviours.

Transl Oncol

November 2023

Queensland University of Technology (QUT), School of Biomedical Sciences, Centre for Genomics and Personalised Health at the Translational Research Institute, Woolloongabba 4102, QLD, Australia; Centre for Cancer Biology, Clinical and Health Sciences, University of South Australia and SA Pathology, Adelaide SA, 5001, Australia; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway; Department of Medical Genetics, Oslo University Hospital, Oslo, Norway. Electronic address:

Epithelial-mesenchymal plasticity (EMP) is a hallmark of cancer. By enabling cells to shift between different morphological and functional states, EMP promotes invasion, metastasis and therapy resistance. We report that near-diploid non-cancerous human epithelial lung cells spontaneously shift along the EMP spectrum without genetic changes.

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Preventive effect of Ya'an Tibetan tea on obesity in rats fed with a hypercaloric high-fat diet revealed by gut microbiology and metabolomics studies.

Food Res Int

March 2023

College of Pharmacy, Zunyi Medical University, Zunyi 563000, China; Queensland University of Technology (QUT), School of Biomedical Sciences, Centre for Genomics and Personalised Health at the Translational Research Institute, Brisbane, QLD 4102, Australia; Key Lab of the Basic Pharmacology of the Ministry of Education, Zunyi Medical University, Zunyi, 563000, China. Electronic address:

Ya'an Tibetan Tea (YATT) is a classic dark tea variety fermented with a unique geographical environment and traditional craftsmanship. Previous research indicates that it is beneficial for obesity and related metabolic disorders, but no systematic research currently reveals its precise mechanisms. This work investigated the preventive effect of YATT on obesity and the corresponding potential mechanisms by performing 16S rRNA gene sequencing and metabolomics studies.

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The radical reactions of dimethylsulfoxide (DMSO) and tetrahydrothiophene-1-oxide (THTO) with reactive oxygen species (ROS) in the presence of a nitroxide radical scavenger have been evaluated both synthetically and in analytical practice. Fenton-mediated generation of oxygen-centred radicals produced several unusual products that reflect the fragmentation and ring-opening radical mechanisms of DMSO and THTO respectively. Addition of pollution-derived ROS to DMSO/THTO nitroxide solutions produced LC-MS detectable amounts of the same products isolated from the larger-scaled Fenton reactions.

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hSSB2 (NABP1) is required for the recruitment of RPA during the cellular response to DNA UV damage.

Sci Rep

October 2021

Cancer & Ageing Research Program, Centre for Genomics and Personalised Health at the Translational Research Institute (TRI), Queensland University of Technology (QUT), Brisbane, Australia.

Article Synopsis
  • Maintaining genomic stability is crucial to prevent diseases like cancer, and cells use various pathways to detect and repair DNA damage caused by factors like UVB radiation, which creates harmful lesions in DNA called cyclobutane pyrimidine dimers (CPD).* -
  • The study focuses on the protein hSSB2, highlighting its increased levels and rapid binding to chromatin after UVB exposure, essential for initiating the repair process.* -
  • Depletion of hSSB2 impairs the recruitment and function of key repair proteins, increasing cellular sensitivity to UVB damage, and indicating its significant role in the nucleotide excision repair (NER) pathway.*
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Genomic stability is critical for normal cellular function and its deregulation is a universal hallmark of cancer. Here we outline a previously undescribed role of COMMD4 in maintaining genomic stability, by regulation of chromatin remodelling at sites of DNA double-strand breaks. At break-sites, COMMD4 binds to and protects histone H2B from monoubiquitination by RNF20/RNF40.

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DNA repair pathways are essential to maintain the integrity of the genome and prevent cell death and tumourigenesis. Here, we show that the Barrier-to-Autointegration Factor (Banf1) protein has a role in the repair of DNA double-strand breaks. Banf1 is characterized as a nuclear envelope protein and mutations in Banf1 are associated with the severe premature aging syndrome, Néstor-Guillermo Progeria Syndrome.

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SASH1 is a prognostic indicator and potential therapeutic target in non-small cell lung cancer.

Sci Rep

October 2020

Cancer and Ageing Research Program, Centre for Genomics and Personalised Health at the Translational Research Institute (TRI), Queensland University of Technology, 37 Kent Street Woolloongabba, Brisbane, 4102, Australia.

SASH1 (SAM and SH3 domain-containing protein 1) is a tumor suppressor protein that has roles in key cellular processes including apoptosis and cellular proliferation. As these cellular processes are frequently disrupted in human tumours and little is known about the role of SASH1 in the pathogenesis of the disease, we analysed the prognostic value of SASH1 in non-small cell lung cancers using publicly available datasets. Here, we show that low SASH1 mRNA expression is associated with poor survival in adenocarcinoma.

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