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Biology of Cancer - Cancer Currents Blog

Cancer biology research news, with context from experts at NCI and elsewhere. Topics include cancer metastasis, the tumor microenvironment, and new targets for cancer therapies.

  • An electron microscope image of a neutrophil ejecting a NET that has captured bacteria
    • By Sharon Reynolds

    Stress-induced hormones called glucocorticoids can cause biological changes—in the form of sticky traps called NETs—that help create hospitable environments for cancer cells to form metastatic tumors, according to new research done largely in mice.

  • An illustration of CAR t-cells and red blood cells on a red background
    • By Sharon Reynolds

    Adding a fusion of parts of two genes helped engineered T cells divide faster, kill more tumor cells, and survive longer in mice without making the T cells behave like cancer cells.

  • An illustration depicting how gene therapy increases the amount of BAMBI in cells.
    • By Sharon Reynolds

    In a new study in mice, researchers showed they could enhance radiation therapy by boosting levels of the BAMBI protein in MDSC immune cells in the tumor microenvironment. After radiation, T cells flooded into the tumor and killed tumors elsewhere in the body.

  • An imaging scan of a brain with a meningioma highlighted in orange.
    • By Sharon Reynolds

    The activity of 34 genes can accurately predict the aggressiveness of meningiomas, a new study shows. This gene expression signature may help oncologists select the best treatments for people with this common type of brain cancer than they can with current methods.

  • An illustration showing how IgA antibodies slip inside a cancer cell, latch onto abnormal proteins, and pull them out of the cell.
    • By Nadia Jaber

    Antibodies currently used in many cancer treatments have only been able to reach proteins outside of cancer cells. In a new study in mice, scientists found a way to target cancer-fueling KRAS and IDH1 proteins buried inside cancer cells.

  • Illustration with T cells transferring mitochondria to cancer cells. The T cells, depicted in blue, contain mitochondria, shown as small pink shapes. A connection is shown between a T cell and a cancer cell, facilitating the transfer of mitochondria. Two cancer cells are depicted in pink, labeled as "Mitochondrial Receiver Cancer Cell" and "Cancer Cell."
    • By Sharon Reynolds

    A new study shows that, in some tumors, a subset of cancer cells can drain mitochondria, the tiny structures within cells that produce energy, from T cells and use them for their own energy needs.

  • A tumor with multicolored cells on the left surrounded by gray immune cells. On the right, a tumor with nearly all yellow cells, surrounded by green immune cells.
    • By Nadia Jaber

    A new study, conducted largely in mice, may help explain why a currently used molecular marker—called mismatch repair deficiency—doesn’t always work to predict which patients will respond to immunotherapies called immune checkpoint inhibitors.

  • A picture of Adan Reinosa in his garage with a piece of a car engine.
    • By Edward Winstead

    The ENLACE study is the first to use cutting-edge technologies to describe the molecular features of colorectal tumors in Hispanic and Latino people. The study’s goals are to improve treatments and increase Hispanic/Latino engagement in cancer research.

  • Illustration depicting the interaction between a modified oncolytic virus, tumor cells, and cancer-fighting T cells. The virus causes tumor cell rupture and releases TGFβ blockers, which inhibit Treg cells, thereby enhancing the efficacy of T cells in fighting cancer.
    • By Shana Spindler

    A cancer-infecting virus engineered to tamp down a tumor’s ability to suppress the immune system shrank tumors in mice, a new study shows. The modified oncolytic virus worked even better when used along with an immune checkpoint inhibitor.

  • An illustration of AML cells floating among other cells
    • By Carmen Phillips

    Researchers have used a form of CRISPR, called base editing, to engineer T cells and hematopoietic stem cells as part of a potential “universal” CAR T-cell therapy for blood cancers. In experiments in mice, the treatment rapidly eliminated tumors, including in mice with acute myeloid leukemia (AML).

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