{
"METABOLOMICS WORKBENCH":{"STUDY_ID":"ST002066","ANALYSIS_ID":"AN003365","VERSION":"1","CREATED_ON":"January 28, 2022, 12:34 am"},

"PROJECT":{"PROJECT_TITLE":"Glutaminase inhibition impairs CD8 T cell activation in STK11/Lkb1 deficient lung cancer","PROJECT_TYPE":"untargeted LCMS metabolomics of GM mice lung tumors upon treatment","PROJECT_SUMMARY":"The tumor microenvironment (TME) contains a rich source of nutrients that sustain cell growth and ultimately facilitate tumor progression. The availability of glucose and glutamine in the TME are essential for the development and activation of effector T cells that exert anti-tumor function. Recently, inhibition of glutaminase, the enzyme that hydrolyzes glutamine to glutamate, has garnered interest as an approach to both decrease tumor metabolism and growth, while increasing available glutamine in the TME for effector T cells. Checkpoint blockade immunotherapy unleashes anti-tumor effector capabilities of T cells, and although there are good responses in many solid tumors, a significant proportion of patients respond poorly. In lung adenocarcinoma, response to immunotherapy is reported to be impaired in KRAS-mutant patients harboring concurrent KEAP1 and STK11/Lkb1 mutations. To investigate the metabolism and immune microenvironment of KRAS-mutant lung adenocarcinoma, we generated a series of murine models that reflect the KEAP1 and STK11/Lkb1 mutational landscape seen in patients. Here we show increased glutamate abundance in the Lkb1-deficient TME associated with CD8 T cell activation in response to anti-PD1 checkpoint immunotherapy. Combination treatment with the glutaminase inhibitor CB-839 inhibited clonal expansion and cytotoxic activation of tumor-infiltrating CD8 T cells. Thus, CD8 T cells exposed to checkpoint immunotherapy have a dependence on glutamine and reliance on glutaminase activity and are negatively impacted by the glutaminase inhibitor in this highly activated state. Therefore, we discern that the combination of immunotherapy and glutaminase inhibition is not efficacious for CD8 T cell activation in the tumor microenvironment.","INSTITUTE":"The Walter and Eliza Hall Institute of Medical Research","LABORATORY":"Kate Sutherland","LAST_NAME":"Best","FIRST_NAME":"Sarah","ADDRESS":"1G, Royal Parade, Parkville VIC 3052","EMAIL":"best@wehi.edu.au","PHONE":"+61-3-9345-2452","PUBLICATIONS":"Glutaminase inhibition impairs CD8 T cell activation in STK11/Lkb1 deficient lung cancer","CONTRIBUTORS":"Sarah A. Best, Patrick M. Gubser, Shalini Sethumadhavan, Ariena Kersbergen, Yashira L. Negrón Abril, Joshua Goldford, Katherine Sellers, Waruni Abeysekera, Alexandra L. Garnham, Jackson A. McDonald, Clare E. Weeden, Dovile Anderson, David Pirman, Thomas P. Roddy, Darren J. Creek, Axel Kallies, Gillian Kingsbury and Kate D. Sutherland"},

"STUDY":{"STUDY_TITLE":"Glutaminase inhibition impairs CD8 T cell activation in STK11/Lkb1 deficient lung cancer","STUDY_TYPE":"Biomedical research","STUDY_SUMMARY":"To characterize the impact of KRAS co-mutations KEAP1 and STK11/Lkb1 on the metabolic and immune microenvironment of lung adenocarcinoma in immune-intact models, we generated a cohort of genetically engineered mouse models (GEMMs) to reflect the diverse tumor suppressor landscape seen in patients. Mice carrying the KrasG12D allele (K)21 were crossed with Keap1flox/flox (KK)22 and/or Lkb1flox/flox (KKL, KL)23 mice and genetic recombination induced by intranasal inhalation of Ad5-CMV-Cre adenovirus. We interrogated the metabolites present in lung tumor nodules collected from cohorts of KK, KL and KKL mice.","INSTITUTE":"The Walter and Eliza Hall Institute of Medical Research","LABORATORY":"Kate Sutherland","LAST_NAME":"Sarah","FIRST_NAME":"Best","ADDRESS":"1G, Royal Parade, Parkville VIC 3052, Australia","EMAIL":"best@wehi.edu.au","PHONE":"+61-3-9345-2452","NUM_GROUPS":"5","TOTAL_SUBJECTS":"25","NUM_MALES":"17","NUM_FEMALES":"8","STUDY_COMMENTS":"L lobe of mice lung","PUBLICATIONS":"Glutaminase inhibition impairs CD8 T cell activation in STK11/Lkb1 deficient lung cancer"},

"SUBJECT":{"SUBJECT_TYPE":"Mammal","SUBJECT_SPECIES":"Mus musculus","TAXONOMY_ID":"10090","GENOTYPE_STRAIN":"C57Bl/6 GEMMs","AGE_OR_AGE_RANGE":"Mutants: K: 90 days, KK: 60 days, KL and KKL: 40 days post Ad5-CMV-Cre","GENDER":"Male and female"},
"SUBJECT_SAMPLE_FACTORS":[
{
"Subject ID":"-",
"Sample ID":"Blank_1",
"Factors":{"treatment":"Extraction blank"},
"Additional sample data":{"RAW_FILE_NAME":"Blank_1"}
},
{
"Subject ID":"-",
"Sample ID":"Blank_2",
"Factors":{"treatment":"Extraction blank"},
"Additional sample data":{"RAW_FILE_NAME":"Blank_2"}
},
{
"Subject ID":"-",
"Sample ID":"Blank_3",
"Factors":{"treatment":"Extraction blank"},
"Additional sample data":{"RAW_FILE_NAME":"Blank_3"}
},
{
"Subject ID":"-",
"Sample ID":"Blank_4",
"Factors":{"treatment":"Extraction blank"},
"Additional sample data":{"RAW_FILE_NAME":"Blank_4"}
},
{
"Subject ID":"-",
"Sample ID":"K_1",
"Factors":{"treatment":"Kras"},
"Additional sample data":{"RAW_FILE_NAME":"K_1"}
},
{
"Subject ID":"-",
"Sample ID":"K_2",
"Factors":{"treatment":"Kras"},
"Additional sample data":{"RAW_FILE_NAME":"K_2"}
},
{
"Subject ID":"-",
"Sample ID":"K_3",
"Factors":{"treatment":"Kras"},
"Additional sample data":{"RAW_FILE_NAME":"K_3"}
},
{
"Subject ID":"-",
"Sample ID":"K_4",
"Factors":{"treatment":"Kras"},
"Additional sample data":{"RAW_FILE_NAME":"K_4"}
},
{
"Subject ID":"-",
"Sample ID":"K_5",
"Factors":{"treatment":"Kras"},
"Additional sample data":{"RAW_FILE_NAME":"K_5"}
},
{
"Subject ID":"-",
"Sample ID":"KK_1",
"Factors":{"treatment":"YFP(WT)/Kras/Keap1/p53(WT)"},
"Additional sample data":{"RAW_FILE_NAME":"KK_1"}
},
{
"Subject ID":"-",
"Sample ID":"KK_2",
"Factors":{"treatment":"Kras/Keap1"},
"Additional sample data":{"RAW_FILE_NAME":"KK_2"}
},
{
"Subject ID":"-",
"Sample ID":"KK_3",
"Factors":{"treatment":"Kras/Keap1"},
"Additional sample data":{"RAW_FILE_NAME":"KK_3"}
},
{
"Subject ID":"-",
"Sample ID":"KK_4",
"Factors":{"treatment":"Kras/Keap1"},
"Additional sample data":{"RAW_FILE_NAME":"KK_4"}
},
{
"Subject ID":"-",
"Sample ID":"KK_5",
"Factors":{"treatment":"Kras/Keap1"},
"Additional sample data":{"RAW_FILE_NAME":"KK_5"}
},
{
"Subject ID":"-",
"Sample ID":"KKL_1",
"Factors":{"treatment":"Kras/Keap1/Lkb1"},
"Additional sample data":{"RAW_FILE_NAME":"KKL_1"}
},
{
"Subject ID":"-",
"Sample ID":"KKL_3",
"Factors":{"treatment":"Kras/Keap1/Lkb1"},
"Additional sample data":{"RAW_FILE_NAME":"KKL_3"}
},
{
"Subject ID":"-",
"Sample ID":"KKL_4",
"Factors":{"treatment":"Kras/Keap1/Lkb1"},
"Additional sample data":{"RAW_FILE_NAME":"KKL_4"}
},
{
"Subject ID":"-",
"Sample ID":"KKL_5",
"Factors":{"treatment":"Kras/Keap1/Lkb1"},
"Additional sample data":{"RAW_FILE_NAME":"KKL_5"}
},
{
"Subject ID":"-",
"Sample ID":"KL_1",
"Factors":{"treatment":"Kras/Lkb1"},
"Additional sample data":{"RAW_FILE_NAME":"KL_1"}
},
{
"Subject ID":"-",
"Sample ID":"KL_2",
"Factors":{"treatment":"Kras/Lkb1"},
"Additional sample data":{"RAW_FILE_NAME":"KL_2"}
},
{
"Subject ID":"-",
"Sample ID":"KL_3",
"Factors":{"treatment":"Kras/Lkb1"},
"Additional sample data":{"RAW_FILE_NAME":"KL_3"}
},
{
"Subject ID":"-",
"Sample ID":"KL_4",
"Factors":{"treatment":"Kras/Lkb1"},
"Additional sample data":{"RAW_FILE_NAME":"KL_4"}
},
{
"Subject ID":"-",
"Sample ID":"KL_5",
"Factors":{"treatment":"Kras/Lkb1"},
"Additional sample data":{"RAW_FILE_NAME":"KL_5"}
},
{
"Subject ID":"-",
"Sample ID":"KP_1",
"Factors":{"treatment":"YFP(WT)/Kras/Keap1(WT)/p53"},
"Additional sample data":{"RAW_FILE_NAME":"KP_1"}
},
{
"Subject ID":"-",
"Sample ID":"KP_2",
"Factors":{"treatment":"Kras/p53"},
"Additional sample data":{"RAW_FILE_NAME":"KP_2"}
},
{
"Subject ID":"-",
"Sample ID":"KP_3",
"Factors":{"treatment":"Kras/p53"},
"Additional sample data":{"RAW_FILE_NAME":"KP_3"}
},
{
"Subject ID":"-",
"Sample ID":"KP_4",
"Factors":{"treatment":"Kras/p53"},
"Additional sample data":{"RAW_FILE_NAME":"KP_4"}
},
{
"Subject ID":"-",
"Sample ID":"QC_1",
"Factors":{"treatment":"QC"},
"Additional sample data":{"RAW_FILE_NAME":"QC_1"}
},
{
"Subject ID":"-",
"Sample ID":"QC_2",
"Factors":{"treatment":"QC"},
"Additional sample data":{"RAW_FILE_NAME":"QC_2"}
},
{
"Subject ID":"-",
"Sample ID":"QC_3",
"Factors":{"treatment":"QC"},
"Additional sample data":{"RAW_FILE_NAME":"QC_3"}
},
{
"Subject ID":"-",
"Sample ID":"QC_4",
"Factors":{"treatment":"QC"},
"Additional sample data":{"RAW_FILE_NAME":"QC_4"}
}
],
"COLLECTION":{"COLLECTION_SUMMARY":"At defined timepoints (K: 90 days, KK: 60 days, KL and KKL: 40 days post Ad5-CMV-Cre), mice were sacrificed by cardiac puncture and lungs and plasma harvested for downstream analysis.","SAMPLE_TYPE":"Lung","STORAGE_CONDITIONS":"-80℃"},

"TREATMENT":{"TREATMENT_SUMMARY":"Mice were genotyped using primers outlined in the Key Resources Table. Seven-to-eight-week old conditional mice were intranasally (i.n) infected with 20 ul of 1x1010 PFU/ml Ad5-CMV-Cre virus (University of Iowa Gene Transfer Core Facility) according to standard procedures62. For anti-PD1 survival study, 20 days following Ad5-CMV-Cre, KL and KKL mice were randomly assigned to anti-PD1 or isotype control antibody (200 g RMP1-14 or Rat IgG2a; BioXCell) treatment arms (n = 6/arm). Each cycle (every 20 days) consisted of intra-peritoneal injection (200 l into left and right flank) three times over 6 days (day 0, 3, 6). Mice were collected at ethical endpoint for Kaplan Meier survival analysis. For combination anti-PD1/CB-839 study, 20 days following Ad5-CMV-Cre, KL mice were randomly assigned to vehicle/isotype, vehicle/anti-PD1, CB-839/isotype or CB-839/anti-PD1 treatment arms (study 1: n = 6/arm; study 2: n = 4/arm). On day 20, mice received one cycle of anti-PD1 or isotype control (as above) and 200 mg/kg CB-839 (2 % w/v CB-839; BLDpharm, in vehicle) or vehicle (20 % Solutol HS15 / 20 % SB-β-CD (Captisol) / 50 mM phosphate buffer, pH 7.4) twice daily by oral gavage until collection on day 29, when mice were collected 12 hours following the final dose. At harvest, mice were sacrificed by cardiac bleed and the left lung lobe was weighed and processed for flow cytometry with spleens, while right lung lobes were inflated with 4 % paraformaldehyde and processed for histology.","TREATMENT_COMPOUND":"200 ug RMP1-14 or Rat IgG2a; Combination treatments: vehicle/isotype, vehicle/anti-PD1, CB-839/isotype or CB-839/anti-PD1 treatment arms","TREATMENT_ROUTE":"by oral gavage","TREATMENT_DOSE":"multiple dose 200 ug. Combination treatments: 200 mg/kg CB-839 (2 % w/v CB-839; BLDpharm, in vehicle) or vehicle (20 % Solutol HS15 / 20 % SB-β-CD (Captisol) / 50 mM phosphate buffer, pH 7.4) twice daily by oral gavage until collection on day 29,"},

"SAMPLEPREP":{"SAMPLEPREP_SUMMARY":"Tumor tissue was flash frozen and crushed using a mortar and pestle in liquid nitrogen. To the Eppendorf tubes 150 µL of cold 80 % acetonitrile was added and vortexed quickly. The suspension was transferred to a fresh Eppendorf tube. Another 150 µL portion of extraction solvent was added to the tubes, vortexed and the suspension combined with the first portion. To the combined extraction mixture 75 µL of CHCl3 was added and samples were mixed for 1 h in a cool room to ensure complete extraction. The samples were centrifuged at 4 °C at 14.8 g for 10 min, supernatant transferred to new tubes and evaporated at 20 °C under a stream of nitrogen. BSA assay was performed on the protein pellet by dissolving all protein in equal volume of detergent solution (4 % v/v SDS in water). Dried samples were resolubilized in appropriate volume of CHCl3 : MeOH : H2O (1 : 3 :1, v/v) mixture based on measured protein content, shaken for 15 min at room temperature, centrifuged at 4 °C at 14.8 g for 10 min. 100 µL of the supernatant was transferred to LCMS vials. 10 µL injected for metabolomics analysis.","PROCESSING_STORAGE_CONDITIONS":"-80℃","EXTRACT_STORAGE":"-80℃"},

"CHROMATOGRAPHY":{"CHROMATOGRAPHY_SUMMARY":"LCMS data was acquired on Q-Exactive Orbitrap mass spectrometer (Thermo Fisher) coupled with high-performance liquid chromatography (HPLC) system Dionex Ultimate® 3000 RS (Thermo Fisher). Chromatographic separation was performed on a ZIC-pHILIC column (5 µm, polymeric, 150 × 4.6 mm, SeQuant®, Merck). The mobile phase (A) was 20 mM ammonium carbonate and (B) acetonitrile. The gradient program started at 80% B and was reduced to 50% B over 15 min, then reduced from 50% B to 5% B over 3 min, followed by wash with 5% B for another 3 min, and finally 8 min re-equilibration with 80% B. The flow rate was 0.3 mL/min and column compartment temperature was 40ºC. The total run time was 32 min with an injection sample volume of 10 µL.","CHROMATOGRAPHY_TYPE":"HILIC","INSTRUMENT_NAME":"Thermo Dionex Ultimate 3000 RS","COLUMN_NAME":"SeQuant ZIC-pHILIC (150 x 4.2 mm, 5 um)","FLOW_GRADIENT":"0 min - 80%B, 15 min - 50%B, 18 min - 5%B, 21 min - 5%B, 24 min - 80%B, 32 min - 80%B","FLOW_RATE":"0.3 ml/min","COLUMN_TEMPERATURE":"25 C","METHODS_FILENAME":"Metabolomics_pHILIC_Parkville_v1.meth","SOLVENT_A":"20 mM ammonium formate","SOLVENT_B":"acetonitrile","COLUMN_PRESSURE":"60 bar at starting conditions","INJECTION_TEMPERATURE":"4 C","INTERNAL_STANDARD":"CAPS, CHAPS, PIPES","SAMPLE_INJECTION":"10 uL","ANALYTICAL_TIME":"32 min","CAPILLARY_VOLTAGE":"3.5 kV","OVEN_TEMPERATURE":"25 C","WASHING_BUFFER":"syringe wash 50% IPA","WEAK_WASH_SOLVENT_NAME":"10% MeOH","STRONG_WASH_SOLVENT_NAME":"10% MeOH","SAMPLE_LOOP_SIZE":"25 uL","SAMPLE_SYRINGE_SIZE":"25 uL"},

"ANALYSIS":{"ANALYSIS_TYPE":"MS","LABORATORY_NAME":"Monash Proteomics and Metabolomics Facility","OPERATOR_NAME":"Dovile Anderson","DETECTOR_TYPE":"Full scan","SOFTWARE_VERSION":"XCalibur","ACQUISITION_DATE":"25/07/2019","ANALYSIS_PROTOCOL_FILE":"PQMS3-MBPF-WIN-0501 LCMS data acquisition for untargeted metabolomics analysis.pdf","ACQUISITION_PARAMETERS_FILE":"Metabolomics_pHILIC_Parkville_v1.pdf","DATA_FORMAT":".RAW"},

"MS":{"INSTRUMENT_NAME":"Thermo Q Exactive Orbitrap","INSTRUMENT_TYPE":"Orbitrap","MS_TYPE":"ESI","ION_MODE":"POSITIVE","MS_COMMENTS":"Mass spectrometer operated in full scan mode with positive and negative polarity switching at 35000 resolution at 200 m/z with detection range of 85 to 1, 275 m/z in full scan mode. Electro-spray ionization source (HESI) was set to 3.5 kV voltage for positive mode and 4.0 kV for negative mode, sheath gas was set to 50 and aux gas to 20 arbitrary units, capillary temperature 300 °C, probe heater temperature 120 °C.","CAPILLARY_TEMPERATURE":"300 C","CAPILLARY_VOLTAGE":"4 kV","COLLISION_ENERGY":"NA","COLLISION_GAS":"NA","ION_SOURCE_TEMPERATURE":"120 C","MASS_ACCURACY":"1-2 ppm","AUTOMATIC_GAIN_CONTROL":"1e6","DATAFORMAT":"profile"},

"MS_METABOLITE_DATA":{
"Units":"peak height",

"Data":[{"Metabolite":"PC(16:0/9:0(CHO))","Blank_1":"0","Blank_2":"112257.9375","Blank_3":"126479.6484","Blank_4":"130180.8359","K_1":"406121.7188","K_2":"385903.25","K_3":"559278.25","K_4":"284969.4688","K_5":"761208.25","KK_1":"474771.4688","KK_2":"438060.4063","KK_3":"434942.9688","KK_4":"937955.3125","KK_5":"703343.5","KKL_1":"398808.6563","KKL_3":"688912","KKL_4":"691036.125","KKL_5":"454088.1563","KL_1":"0","KL_2":"901185.875","KL_3":"192946.0313","KL_4":"135493.9531","KL_5":"387771.875","KP_1":"693362.0625","KP_2":"535821.4375","KP_3":"775914.5625","KP_4":"654462.875","QC_1":"769628.0625","QC_2":"578472.9375","QC_3":"630205.5625","QC_4":"575087.8125"},{"Metabolite":"alpha-(2,6-anhydro-3-deoxy-D-arabino-heptulopyranosid)onate 7-phosphate","Blank_1":"0","Blank_2":"0","Blank_3":"0","Blank_4":"0","K_1":"79776.02344","K_2":"170382.0938","K_3":"216619.8906","K_4":"228512.5938","K_5":"284904.2813","KK_1":"71128.45313","KK_2":"85587.3125","KK_3":"60115.30859","KK_4":"57320.51172","KK_5":"44118.34766","KKL_1":"115859.6484","KKL_3":"127564.9063","KKL_4":"89769.21094","KKL_5":"98379.89844","KL_1":"199403.9688","KL_2":"208127.5625","KL_3":"136466.2969","KL_4":"194105.2188","KL_5":"253188.7188","KP_1":"162968.0313","KP_2":"241451.5469","KP_3":"48632.10938","KP_4":"76093.27344","QC_1":"175557.4531","QC_2":"218921.4531","QC_3":"210545.0469","QC_4":"121903.6328"},{"Metabolite":"alpha-oxo-1-carboxy-5,6-dihydrothiopyranpropanoate 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}