Toggle light / dark theme

Hepatocellular carcinoma (HCC) is the most common primary liver cancer, affecting millions of people worldwide. Due to the complexity and variability of the disease, there are major challenges in the treatment of HCC in its intermediate and advanced stages; despite advances in various treatment modalities, there are still gaps in our understanding of effective therapeutic strategies. Key findings from several studies have shown that the combination of immunotherapy and targeted therapy has a synergistic anti-tumor effect, which can significantly enhance efficacy with a favorable safety profile. In addition, other studies have identified potential biomarkers of therapeutic response, such as tumor protein 53 (TP53) and CTNNB1 (encoding β-conjugated proteins), thus providing personalized treatment options for patients with intermediate and advanced hepatocellular carcinoma. The aim of this article is to review the recent advances in the treatment of intermediate and advanced HCC, especially targeted immune-combination therapy, chimeric antigen receptor T cell therapy (CAR-T cell therapy), and gene therapy for these therapeutic options that fill in the gaps in our knowledge of effective treatment strategies, providing important insights for further research and clinical practice.

Hepatocellular carcinoma is a common malignant tumor, ranking sixth and fifth in incidence globally and in China, respectively. It ranks among the top three in mortality and has long been recognized as a global challenge. HCC is the most common type of liver cancer, accounting for 75% to 80% of cases. Its incidence and mortality vary significantly across regions, which is closely related to risk factors such as viral hepatitis (e.g., hepatitis B and C), alcoholic and non-alcoholic cirrhosis, and fatty liver. Treatment options for HCC include surgical resection, percutaneous anhydrous ethanol injection, Transcatheter arterial embolization (TACE), ablative therapy, chemotherapy and liver transplantation. Early stage HCC can be completely cured by surgery, but about 70% of patients have progressed to an intermediate and advanced stage at the time of diagnosis and are unable to undergo surgery.

A disrupted protein degradation process in heart muscle cells can lead to a range of severe heart diseases. In the case of dilated cardiomyopathy, a pathological enlargement of the heart chambers, researchers at the Max Planck Institute for Heart and Lung Research in Bad Nauheim have now identified a cause: a low level of the enzyme Ubiquitin-specific peptidase 5 (USP5) leads to an accumulation of Ubiquitin in heart muscle cells and the formation of protein aggregates, which trigger heart diseases. Increasing USP5 levels in heart muscle cells protects the heart from harmful degradation processes, offering a perspective for new therapies.

Dilated cardiomyopathy is a pathological enlargement of one or both heart chambers, including the atria. The resulting restriction of heart function is caused by structural damage to . The consequence is , which can lead to death without a heart transplant. Existing can usually not stop or reverse the progression of the disease.

In search of new therapeutic approaches, researchers from the department of Thomas Braun at the Max Planck Institute for Heart and Lung Research have investigated the molecular processes of protein degradation in heart muscle cells. Yvonne Eibach and Silke Kreher, both first authors of the study published in Science Advances, together with their research partners, discovered disturbances in the process that serves the disposal of defective or no longer needed proteins.

An international team of scientists has modeled the formation and evolution of the strongest magnetic fields in the universe.

Led by scientists from Newcastle University, University of Leeds and France, the paper was published in the journal Nature Astronomy. The researchers identified the Tayler-Spruit dynamo caused by the fall back of supernova material as a mechanism leading to the formation of low-field magnetars. This new work solves the mystery of low-field formation, which has puzzled scientists since low-field magnetar discovery in 2010.

The team used advanced numerical simulations to model the magneto-thermal evolution of these stars, finding that a specific dynamo process within the proto-neutron star can generate these weaker magnetic fields.

On a clear spring evening in Michigan, the stars aligned — just not in the way Upfront Ventures partner Nick Kim expected.

He’d just led a $9.5 million seed round for OurSky, a software platform for space observational data, and was eager to see what its telescope partner PlaneWave Instruments could do.

But when they rolled out the telescopes that night at PlaneWave’s manufacturing facility, he was stuck waiting.