Malignant mesothelioma (MM) is an aggressive tumour that commonly affects the mesothelial surfaces of the pleural and peritoneal cavities, and occasionally, the tunica vaginalis and the pericardium. Formerly a rare tumour, MM is increasing in incidence in Australia due to the heavy nationwide use of asbestos from 1940 until the 1980s. The incidence is expected to peak in Australia in the next decade, mirroring the long latency period between asbestos exposure and development of MM. Diagnosis of MM can be difficult. Definitive pathological diagnosis is required and it often requires an experienced pathologist to differentiate MM from other benign or malignant processes. Treatment of MM requires a multidisciplinary approach, regardless of palliative or curative intent. Treatment options, such as surgery, chemotherapy, radiotherapy and active symptom control or a combination of these, may be used. Further research is needed to advance the therapeutic options for MM, and strategies to realize personalisation of therapy through discovery of predictive markers. In the Australian society where asbestos contamination of the built environment is very high, education and stringent public health measures are required to prevent a second wave of increased MM incidence.
Background: KRAS mutant non-small cell lung cancers (NSCLC) bearing co-mutations in LKB1 (KL tumors) have a distinct biology, molecular vulnerabilities, and therapeutic sensitivities. KL tumors are characterized by upregulation of the NRF2/KEAP1 pathway which may serve as a compensatory mechanism to maintain redox homeostasis in the face of oxidative stress. The NRF2/KEAP1 pathway plays a role in regulating glutathione synthesis from glutamate. We hypothesized that glutaminase inhibition would reduce intracellular glutamate, reduce the ability to tolerate oxidative stress, and enhance radiotherapy sensitivity in KL tumors with KEAP1/NRF2 pathway upregulation. Method: Expression of NRF2 and NRF2 related genes were analyzed by Western blotting in isogenic KRAS-mutant LKB1 deficient/proficient NSCLC cell lines. Intracellular reactive oxygen species (ROS) levels were monitored using 2'7'-dichlorofluorescein (DCFDA) and flow cytometry. Cell apoptosis analysis was determined using PE-conjugated annexin-V/7-AAD staining and carried out by flow cytometry. Cell growth was evaluated by Cell Titer Glo Assays. Ionizing radiation sensitivity was assessed by clonogenic cell survival assay (CSA). Result: LKB1 loss increased ROS accumulation and resulted in upregulation of NRF2 and NRF2 target genes in isogenic KRAS-mutant cell lines. KL cells were significantly more resistant to ROS than cells with KRAS mutation alone, as determined by the treatment with the ROS donor H 2 O 2. NRF knockdown abrogated this resistance to in KL cells. KL cells also were more resistant to radiotherapy. Re-expression of LKB1 or NRF2 pathway suppression (via KEAP1 expression or NRF2 knockdown) enhanced radiotherapy sensitivity as measured by CSA with a dose enhancement ratio (DER) 1.6 and 1.2, respectively, at a surviving fraction of 0.5. The glutaminase inhibitor CB839 enhanced the radio-sensitivity of KL cells with NRF2 pathway activation (via KEAP1 mutation). Re-expression of LKB1 or NRF2 pathway suppression abrogated the CB839-induced radiosensitization. Conclusion: Our results suggest that upregulation of the NRF2/KEAP1 pathway in NSCLC bearing co-mutations in KRAS and LKB1 is critical to maintain redox homeostasis and GLS inhibition can sensitize KL tumors to radiotherapy in an LKB1-and KEAP1/NRF2-dependent manner.
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