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Researchers at the University of Cologne discovered a new mechanism used by one of the most aggressive forms of lung cancer to escape treatment, paving the way for more efficient future therapies / publication in “Nature Communications”
Small cell lung cancer (SCLC) is one of the most aggressive forms of lung cancer, with a five-year survival rate of only five percent. Despite this poor prognosis, SCLC is initially highly responsive to chemotherapy. However, patients typically relapse and experience very rapid disease progression. Current research into the biological mechanisms behind SCLC remains essential in order to prolong treatment responses, overcome relapse and, ultimately, improve long-term patient outcomes.
A research team led by Professor Dr Silvia von Karstedt (Translational Genomics, CECAD Cluster of Excellence on Aging Research, and Center for Molecular Medicine Cologne – CMMC) has discovered a novel mechanism used by this type of cancer that helps explain its aggressive nature. The study titled “Lack of Caspase 8 Directs Neuronal Progenitor-like reprogramming and Small Cell Lung Cancer Progression” was published in Nature Communications.
Unlike other epithelial cancers, SCLC shares features with neuronal cells, including lack of caspase-8 expression, a protein involved in programmed, non-inflammatory cell-death (apoptosis), a mechanism that is essential to eliminate faulty or mutated cells and to maintain health.
To better mimic the features of human SCLC, the team generated and characterized a novel genetically engineered mouse model lacking caspase-8. Using this new model, the team observed that when this protein is missing, an unusual chain reaction sets off. “The absence of caspase-8 leads to a type of inflammatory cell death called necroptosis that creates a hostile, inflamed environment even before tumors fully form” explains von Karstedt. “We were also intrigued to find that pre-tumoral necroptosis can in fact promote cancer by conditioning the immune system,” she continues. The inflammation creates an environment where the body’s anti-cancer immune response is suppressed, preventing immune cells from attacking threats like cancer cells. This, in turn, can promote tumour metastasis. Surprisingly, the researchers observed that this inflammation also pushes the cancer cells to behave more like immature neuron-like cells, a state that makes them better at spreading and that is associated with relapse.
While it remains unknown whether similar pre-tumoral inflammation also occurs in human patients, this work identifies a mechanism contributing to the aggressiveness and patient relapse in SCLC that could be exploited as a way to improve the efficiency of future therapies and early-stage diagnostic methods.
This research was supported by the German Research Foundation within Collaborative Research Centre (CRC) 1399 “Mechanisms of drug sensitivity and resistance in small cell lung cancer”.
Professor Dr Silvia von Karstedt
Department of Translational Genomics, University Hospital Cologne
+49 221 478 84340
s.vonkarstedt@uni-koeln.de
https://www.nature.com/articles/s41467-025-67142-4
CD45 staining of lung alveolar tissue of a novel SCLC mouse model. In these mice there is increased ...
Source: Ariadne Androulidaki
Copyright: Universität zu Köln
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CD45 staining of lung alveolar tissue of a novel SCLC mouse model. In these mice there is increased ...
Source: Ariadne Androulidaki
Copyright: Universität zu Köln
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