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Mashup Score: 18
Abstract. Cancer homeostasis depends on a balance between activated oncogenic pathways driving tumorigenesis and engagement of stress-response programs that counteract the inherent toxicity of such aberrant signaling. While inhibition of oncogenic signaling pathways has been explored extensively, there is increasing evidence that overactivation of the same pathways can also disrupt cancer homeostasis and cause lethality. We show here that inhibition of Protein Phosphatase 2A (PP2A) hyperactivates multiple oncogenic pathways and engages stress responses in colon cancer cells. Genetic and compound screens identify combined inhibition of PP2A and WEE1 as synergistic in multiple cancer models by collapsing DNA replication and triggering premature mitosis followed by cell death. This combination also suppressed the growth of patient-derived tumors in vivo. Remarkably, acquired resistance to this drug combination suppressed the ability of colon cancer cells to form tumors in vivo. Our data s
Source: aacrjournals.orgCategories: General Medicine News, Hem/OncsTweet
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Mashup Score: 18
Abstract. Cancer homeostasis depends on a balance between activated oncogenic pathways driving tumorigenesis and engagement of stress-response programs that counteract the inherent toxicity of such aberrant signaling. While inhibition of oncogenic signaling pathways has been explored extensively, there is increasing evidence that overactivation of the same pathways can also disrupt cancer homeostasis and cause lethality. We show here that inhibition of Protein Phosphatase 2A (PP2A) hyperactivates multiple oncogenic pathways and engages stress responses in colon cancer cells. Genetic and compound screens identify combined inhibition of PP2A and WEE1 as synergistic in multiple cancer models by collapsing DNA replication and triggering premature mitosis followed by cell death. This combination also suppressed the growth of patient-derived tumors in vivo. Remarkably, acquired resistance to this drug combination suppressed the ability of colon cancer cells to form tumors in vivo. Our data s
Source: aacrjournals.orgCategories: General Medicine News, Hem/OncsTweet
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Mashup Score: 12Chromosome evolution screens recapitulate tissue-specific tumor aneuploidy patterns - 2 month(s) ago
Nature Genetics – This study examines karyotypic selection and evolution in vitro using immortalized mammary and kidney epithelial cell lines, observing aneuploidy patterns specific to each origin…
Source: www.nature.comCategories: General Medicine News, Oncologists1Tweet
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Mashup Score: 6
Nature – Scientists spot a particle of intense energy, but explaining where it came from might require some new physics.
Source: www.nature.comCategories: General Medicine News, Hem/OncsTweet
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Mashup Score: 3Fixed Term (12 months) up to 3.0FTE Postgraduate Fellow - Radiation Oncology - Westmead Hospital | APPLY VIA ECREDENTIAL | I work for NSW - 8 month(s) ago
Fixed Term (12 months) up to 3.0FTE Postgraduate Fellow Department of Radiation Oncology Westmead Hospital CLICK HERE TO APPLY Applications are inv…
Source: iworkfor.nsw.gov.auCategories: Latest Headlines, Oncologists1Tweet
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Mashup Score: 4Need for Evidence-Based Adoption of New Technologies in Radiotherapy - 9 month(s) ago
This Viewpoint discusses the need for multi-institutional prospective randomized trials of new technologies in radiotherapy to improve the therapeutic ratio and safety of radiotherapy treatments.
Source: jamanetwork.comCategories: Hem/Oncs, Latest HeadlinesTweet
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Mashup Score: 3A survey of CIN measures across mechanistic models - 11 month(s) ago
Chromosomal instability (CIN) is the persistent reshuffling of cancer karyotypes via chromosome mis-segregation during cell division. In cancer, CIN exists at varying levels that have differential effects on tumor progression. However, mis-segregation rates remain challenging to assess in human cancer despite an array of available measures. We evaluated measures of CIN by comparing quantitative…
Source: bioRxivCategories: Hem/Oncs, Latest HeadlinesTweet
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Mashup Score: 0
The switch from glucose- to fatty acid-dependent metabolism in cardiomyocytes of newborn mice is governed by γ-linolenic acid in maternal milk, which binds to retinoid X receptors, thereby causing a transcription-dependent metabolic transition.
Source: NatureCategories: Latest Headlines, Oncologists1Tweet
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Mashup Score: 10
This cross-sectional study assesses the frequency of reporting of primary end point changes among active oncology phase 3 randomized clinical trials.
Source: jamanetwork.comCategories: Hem/Oncs, Latest HeadlinesTweet
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Mashup Score: 2How a simple idea to share lab materials led to a circular-economy movement in science - 12 month(s) ago
Garry Cooper’s sustainability business has grown to help thousands of people conduct more efficient research.
Source: www.nature.comCategories: Hem/Oncs, Latest HeadlinesTweet
When too much of a good thing ends badly... super cool new paper showing that over activation of oncogenic signaling pathways leads to cell death @CD_AACR @MedemaRene https://t.co/Q754IPNG4C