From the blog

Cell Mutations and Peritoneal Mesothelioma

Published: September 19, 2025

Peritoneal mesothelioma is a hard cancer to treat because it is very aggressive and rare. It is usually found late due to it being rare and having unclear symptoms, making treatment very difficult. Current treatments that can include surgery and chemotherapy have limited success against the cancer. New ways to treat peritoneal mesothelioma need to be found in order to better the lives of mesothelioma patients around the world. A new study in Clinical and Experimental Medicine used cutting edge NGS technology to study tumor samples and genetic problems in order to make better treatments.

There is a genetic component to most cancers, including mesothelioma. Mesothelioma researchers around the world are looking into genetic alterations that can help guide treatment. Recent genomic profiling advances are bringing hope to mesothelioma patients. They reveal the disease’s genetic makeup and pinpoint genetic mutations to guide treatment. A new study used NGS technology to study tumor samples from 20 mesothelioma patients. Thorough analysis revealed many genetic problems, shedding light on possible treatments.

The study found many common mutations, including BAP1 mutations standing out at 32 percent. BAP1 is a gene mutation that fights tumors. BAP1 is crucial for cell functions related to cancer development. Even without specific BAP1 treatments available, there are exciting possibilities for intervention. BAP1’s role in DNA repair pathways offers hope for targeted therapy. Mutations in CDKN2A/B and NF2 were found in 16 percent of cases. Mutations create opportunities for targeted treatments. NF2 mutations could benefit from kinase inhibitors like everolimus and temsirolimus, showing promise in research.

There are also ATM mutations, which are less common at 11 percent, that are still important for treatment. These mutations suggest increased sensitivity to PARP inhibitors, leading the way for personalized medicine based on individual genetic makeup. Study results give mesothelioma patients hope, but there are still challenges ahead. We still need to overcome obstacles to turn genomic discoveries into effective treatments. Understanding tumor differences and unknown gene variations is complex, so we must keep studying and interpreting them carefully. Genomic analysis is revolutionizing mesothelioma treatment. It uncovers genetic secrets and helps to create new treatments. Advances in precision oncology allow for personalized care based on genes. Despite challenges, each genetic discovery brings us closer to beating peritoneal mesothelioma with precision medicine.

This is why mesothelioma research is so important. Mesothelioma is a hard cancer to treat, so all the work that goes into defeating the cancer is necessary. People are unnecessarily dying due to asbestos exposure. If a cure can be found for mesothelioma, many people could one day live longer and better lives after a diagnosis.

Source:
Job P. van Kooten et al., “Genomic characterization and detection of potential therapeutic targets for peritoneal mesothelioma in current practice”  Clinical and Experimental Medicine (April 21, 2024). [Link]
Contact Us
CONTACT INFORMATION
DIAGNOSIS
Have you received a diagnosis? *
reCAPTCHA