First human SMUG1 structures reveal how cells repair DNA
Peer-Reviewed Publication
Updates every hour. Last Updated: 23-Jun-2026 14:16 ET (23-Jun-2026 18:16 GMT/UTC)
Researchers have captured the first atomic structures of human SMUG1, an enzyme that helps cells repair damaged DNA. The findings provide new insight into how cells recognise and remove harmful DNA bases, and may support future efforts to develop drugs that target this DNA repair pathway.
Biological tissues can behave like fluids or solids, depending on mechanical properties like tissue rigidity. EMBL researchers and their collaborators have shown that the rigidity of embryonic tissues is directly regulated by factors like cell-cell adhesion – how tightly neighbouring cells connect to each other. They also show that tissue rigidity plays a critical role in tissue organisation, regulating how cells process biochemical information, ultimately determining their future identities in a maturing embryo. These new biophysical findings have important implications for what we know about embryonic development, as well as other processes involving tissue-level transitions, such as cancer metastasis.
After surgery for colon cancer, many patients face the question of whether follow-up chemotherapy is necessary to prevent a possible relapse. The decision is particularly difficult in so-called Stage II, the intermediate-risk group: Although around one in five untreated patients suffers a relapse, adjuvant chemotherapy places a significant and, in some cases, unnecessary burden on many patients. A large clinical study led by Dresden University Hospital (UKD) now provides important insights for a robust basis for decision-making. These findings were presented for the first time at this year’s annual meeting of the American Society of Clinical Oncology (ASCO) and published simultaneously in the Annals of Oncology.