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    • RAS Mutation Tropism
      , by Siqi Li, David MacAlpine, and Christopher M Counter

      The three isoforms of Ras share signaling modalities, yet their cancer-associated mutations vary widely in sequence and the organs affected. Sequencing those mutations very soon after they occur sheds light on the forces driving those differences.

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    • The disease burden of Ras
      , by Ian A Prior

      Cancer genome databases yield different estimates of the importance of RAS genes in cancers. Integrating the data that underlie those estimates may suggest new research priorities based on patient numbers.

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    • Alternative cells-of-origin influence the heterogeneity of KRAS-mutant lung adenocarcinoma
      , by Sarah Best and Kate Sutherland

      The biology of lung cancers driven by mutant KRAS is substantially influenced by the particular cell type in which the KRAS mutation arose. Understanding how the cell of origin and its surroundings react to mutant KRAS suggest therapeutic approaches.

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    • The RASopathies Network
      , by Lisa Schoyer and Beth Stronach

      RASopathies are neurodevelopmental genetic syndromes caused by germline mutations in RAS pathway genes that result in increased MAPK signaling. The RASopathies Network provides an umbrella organization to connect affected families with researchers.

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    • Intravenous High-Dose Vitamin C in Cancer Therapy
      , by Lewis Cantley and Jihye Yun

      Pharmacologic levels of vitamin C in plasma can only be achieved by intravenous administration. Vitamin C undermines RAS-mutant cells’ reliance on upregulation of glycolysis and antioxidant activities to support their cancer lifestyle.

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