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    TRACERx - 1 year(s) ago

    Cancers evolve at a dynamic pace to adapt to immune pressure, colonize new niches, and evade therapy. Tracking these changes can help us improve diagnosis, …

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    • Pretty sure a world record was set yesterday: @CharlesSwanton published 7 (SEVEN) papers in Nature in 1 day. 🤯 Hot diggity damn. https://t.co/vLc4nUMAaI

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    Li et al. uncover crosstalk between core immunogenic, metabolic, and oncogenic pathways in cancer cells during immunotherapy, which enables hyperprogressive disease (HPD) in preclinical models and correlates with immunotherapy-associated HPD in patients with cancer.

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    • About 10% of patients experience hyper-progression after immunotherapy. This very cool paper shows that it is the beloved CD8+ T cells that drive cancer hyperprogression via IFNÎł! This alters B-catenin signaling. Great work! https://t.co/UFOdXhREVN

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    Thank You for Supporting Female Oncologists! We are currently raising funds for the 2023 Women Leaders of Oncology Women Who Conquer Cancer Young Investigator Award. All additional funds will go toward our goal of raising $1.35 million for the Conquer Cancer-Women Leaders in Oncology Young Investigator Award Endowment. This will help ensure that female scientists can receive…

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    • Women are 30% less likely than their male counterparts to receive NIH funding. Women Who Conquer Cancer @ConquerCancerFd and Women Leaders in Oncology #WLO2022 help support young female investigators. Your donation can change a woman's career! https://t.co/m8BuUb55lC

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    Haematopoiesis has high clonal diversity up to about 65 years of age, after which diversity drops precipitously owing to positive selection acting on a handful of clones that expand exponentially throughout adulthood.

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    • As we age, clonal diversity of blood cells decreases. And sorry men, but loss of the Y chromosome was frequent (females do not lose an inactive X chromosome) and this loss was positively selected for! So...X chromosomes rule, just sayin https://t.co/utTos6nqHo