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Published in 2020 at "Cell"
DOI: 10.1016/j.cell.2020.06.013
Abstract: To explore the biology of lung adenocarcinoma (LUAD) and identify new therapeutic opportunities, we performed comprehensive proteogenomic characterization of 110 tumors and 101 matched normal adjacent tissues (NATs) incorporating genomics, epigenomics, deep-scale proteomics, phosphoproteomics, and…
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Keywords:
lung adenocarcinoma;
characterization reveals;
therapeutic vulnerabilities;
proteogenomic characterization ... See more keywords
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Published in 2021 at "iScience"
DOI: 10.1016/j.isci.2021.102522
Abstract: Summary Lung adenocarcinoma (LUAD) patients in East Asia predominantly harbor oncogenic EGFR mutations. However, there remains a limited understanding of the biological characteristics and therapeutic vulnerabilities of the concurrent mutations of EGFR and other genes…
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Keywords:
lung adenocarcinoma;
mutation;
characteristics therapeutic;
therapeutic vulnerabilities ... See more keywords
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Published in 2019 at "Nature Reviews Cancer"
DOI: 10.1038/s41568-019-0169-x
Abstract: The spectrum of tumours arising in childhood is fundamentally different from that seen in adults, and they are known to be divergent from adult malignancies in terms of cellular origins, epidemiology, genetic complexity, driver mutations…
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Keywords:
characteristics therapeutic;
therapeutic vulnerabilities;
vulnerabilities across;
paediatric solid ... See more keywords
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Published in 2020 at "Neuro-oncology"
DOI: 10.1093/neuonc/noaa215.315
Abstract: Meningioma treatments are limited due to incomplete understanding of meningioma biology. To address this, we performed multiplatform molecular profiling on 565 meningiomas with comprehensive clinical data to define genomic drivers and identify therapeutic vulnerabilities. DNA…
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Keywords:
meningiomas;
genomic instability;
therapeutic vulnerabilities;
meningioma ... See more keywords
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Published in 2020 at "Neuro-Oncology"
DOI: 10.1093/neuonc/noaa222.314
Abstract: Abstract INTRODUCTION We have observed that approximately 26% of recurrent gliomas acquire hypermutation following treatment with temozolomide (TMZ). Intriguingly, 91% of these tumors harbor mutations in mismatch repair (MMR) genes. Strategies to target MMR-deficient gliomas…
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Keywords:
deficient gliomas;
therapeutic vulnerabilities;
gliomas;
mismatch repair ... See more keywords
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Published in 2019 at "Cancer research"
DOI: 10.1158/0008-5472.can-18-3704
Abstract: Malignant peripheral nerve sheath tumor (MPNST) is an aggressive sarcoma with recurrent loss-of-function alterations in polycomb-repressive complex 2 (PRC2), a histone-modifying complex involved in transcriptional silencing. To understand the role of PRC2 loss in pathogenesis…
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Keywords:
therapeutic vulnerabilities;
malignant peripheral;
loss;
nerve sheath ... See more keywords
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Published in 2018 at "Translational lung cancer research"
DOI: 10.21037/tlcr.2018.09.10
Abstract: In the last three decades, 5-year relative survival rates for lung cancer improved slightly, from 14.3%, 15.5%, and 18.4% (1). One of the reasons for these dismal survival rates is that most patients present with…
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Keywords:
identifying therapeutic;
vulnerabilities lung;
therapeutic vulnerabilities;
chemistry ... See more keywords
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Published in 2022 at "Cancers"
DOI: 10.3390/cancers14153645
Abstract: Simple Summary Loss of SMARCB1 has been identified as the sole mutation in a number of rare pediatric and adult cancers, most of which have a poor prognosis despite intensive therapies including surgery, radiation, and…
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Keywords:
loss smarcb1;
smarcb1 deficient;
deficient;
tumor ... See more keywords
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Published in 2018 at "International Journal of Molecular Sciences"
DOI: 10.3390/ijms19123987
Abstract: While significant progress has been made in the treatment of acute myeloid leukemia (AML), not all patients can be cured. Mutated in about 1/3 of de novo AML, the FLT3 receptor tyrosine kinase is an…
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Keywords:
therapeutic vulnerabilities;
flt3;
flt3 itd;
aml ... See more keywords
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Published in 2022 at "Oncology Letters"
DOI: 10.3892/ol.2022.13312
Abstract: Retinoblastoma (RB) is a pediatric ocular malignancy that is initiated mostly by biallelic inactivation of the RB transcriptional corepressor 1 (RB1) tumor suppressor gene in the developing retina. Unlike the prevailing prediction based on multiple…
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Keywords:
maintenance;
maintenance retinoblastoma;
genome maintenance;
maintenance mechanisms ... See more keywords