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  1. Article

    Open Access

    Author Correction: Pathway level subty** identifies a slow-cycling biological phenotype associated with poor clinical outcomes in colorectal cancer

    Sudhir B. Malla, Ryan M. Byrne, Maxime W. Lafarge, Shania M. Corry in Nature Genetics (2024)

  2. Article

    Open Access

    Pathway level subty** identifies a slow-cycling biological phenotype associated with poor clinical outcomes in colorectal cancer

    Molecular stratification using gene-level transcriptional data has identified subtypes with distinctive genotypic and phenotypic traits, as exemplified by the consensus molecular subtypes (CMS) in colorectal c...

    Sudhir B. Malla, Ryan M. Byrne, Maxime W. Lafarge, Shania M. Corry in Nature Genetics (2024)

  3. No Access

    Article

    Therapeutic targeting of tumour myeloid cells

    Myeloid cells are pivotal within the immunosuppressive tumour microenvironment. The accumulation of tumour-modified myeloid cells derived from monocytes or neutrophils — termed ‘myeloid-derived suppressor cell...

    Simon T. Barry, Dmitry I. Gabrilovich, Owen J. Sansom in Nature Reviews Cancer (2023)

  4. Article

    Open Access

    MmCMS: mouse models’ consensus molecular subtypes of colorectal cancer

    Colorectal cancer (CRC) primary tumours are molecularly classified into four consensus molecular subtypes (CMS1–4). Genetically engineered mouse models aim to faithfully mimic the complexity of human cancers a...

    Raheleh Amirkhah, Kathryn Gilroy, Sudhir B. Malla in British Journal of Cancer (2023)

  5. No Access

    Article

    The amino acid transporter SLC7A5 is required for efficient growth of KRAS-mutant colorectal cancer

    Oncogenic KRAS mutations and inactivation of the APC tumor suppressor co-occur in colorectal cancer (CRC). Despite efforts to target mutant KRAS directly, most therapeutic approaches focus on downstream pathways,...

    Arafath K. Najumudeen, Fatih Ceteci, Sigrid K. Fey, Gregory Hamm in Nature Genetics (2021)

  6. Article

    Open Access

    Melanoma tumor growth is accelerated in a mouse model of sickle cell disease

    The effect of sickle cell disease (SCD) on tumor growth is unknown. Sickled red blood cells may form aggregates within the microvasculature of hypoxic tumors and reduce blood flow leading to impairment of tumo...

    **tao Wang, Jennifer Tran, Hui Wang, Wei Luo in Experimental Hematology & Oncology (2015)