#METABOLOMICS WORKBENCH metabolic_charlie_20220513_001750 DATATRACK_ID:3247 STUDY_ID:ST002167 ANALYSIS_ID:AN003550 PROJECT_ID:PR001376 VERSION 1 CREATED_ON May 16, 2022, 7:14 am #PROJECT PR:PROJECT_TITLE Remote solid cancers rewire hepatic nitrogen metabolism via host PR:PROJECT_TITLE nicotinamide-N-methyltransferase PR:PROJECT_SUMMARY Cancers disrupt host homeostasis in various manners but the identity of host PR:PROJECT_SUMMARY factors underlying such disruption remains largely unknown. Here we show that PR:PROJECT_SUMMARY nicotinamide-N-methyltransferase (NNMT) is a novel host factor that mediates PR:PROJECT_SUMMARY metabolic dysfunction in the livers of cancer-bearing mice. Multiple solid PR:PROJECT_SUMMARY cancers distantly increase expression of Nnmt and its product PR:PROJECT_SUMMARY 1-methylnicotinamide (MNAM) in the liver. Multi-omics analyses reveal PR:PROJECT_SUMMARY suppression of the urea cycle accompanied by accumulation of amino acids, and PR:PROJECT_SUMMARY enhancement of uracil biogenesis in the livers of cancer-bearing mice. PR:PROJECT_SUMMARY Importantly, genetic deletion of Nnmt leads to alleviation of these metabolic PR:PROJECT_SUMMARY abnormalities, and buffers cancer-dependent weight loss and reduction of the PR:PROJECT_SUMMARY voluntary wheel-running activity. Our data also demonstrate that MNAM is capable PR:PROJECT_SUMMARY of affecting urea cycle metabolites in the liver. These results suggest that PR:PROJECT_SUMMARY cancers up-regulate the hepatic NNMT pathway to rewire liver metabolism towards PR:PROJECT_SUMMARY uracil biogenesis rather than nitrogen disposal via the urea cycle, thereby PR:PROJECT_SUMMARY disrupting host homeostasis. PR:INSTITUTE Tohoku University PR:LAST_NAME Kawaoka PR:FIRST_NAME Shinpei PR:ADDRESS 4-1 Seiryo-cho, Sendai, Miyagi, 9808575, Japan PR:EMAIL kawaokashinpei@gmail.com PR:PHONE 0227178568 #STUDY ST:STUDY_TITLE Remote solid cancers rewire hepatic nitrogen metabolism via host ST:STUDY_TITLE nicotinamide-N-methyltransferase (AML cells) ST:STUDY_SUMMARY Cancers disrupt host homeostasis in various manners but the identity of host ST:STUDY_SUMMARY factors underlying such disruption remains largely unknown. Here we show that ST:STUDY_SUMMARY nicotinamide-N-methyltransferase (NNMT) is a novel host factor that mediates ST:STUDY_SUMMARY metabolic dysfunction in the livers of cancer-bearing mice. Multiple solid ST:STUDY_SUMMARY cancers distantly increase expression of Nnmt and its product ST:STUDY_SUMMARY 1-methylnicotinamide (MNAM) in the liver. Multi-omics analyses reveal ST:STUDY_SUMMARY suppression of the urea cycle accompanied by accumulation of amino acids, and ST:STUDY_SUMMARY enhancement of uracil biogenesis in the livers of cancer-bearing mice. ST:STUDY_SUMMARY Importantly, genetic deletion of Nnmt leads to alleviation of these metabolic ST:STUDY_SUMMARY abnormalities, and buffers cancer-dependent weight loss and reduction of the ST:STUDY_SUMMARY voluntary wheel-running activity. Our data also demonstrate that MNAM is capable ST:STUDY_SUMMARY of affecting urea cycle metabolites in the liver. These results suggest that ST:STUDY_SUMMARY cancers up-regulate the hepatic NNMT pathway to rewire liver metabolism towards ST:STUDY_SUMMARY uracil biogenesis rather than nitrogen disposal via the urea cycle, thereby ST:STUDY_SUMMARY disrupting host homeostasis. Anionic polar metabolites (i.e., organic acids, ST:STUDY_SUMMARY sugar phosphates, nucleotides, etc.) were analyzed via IC/HR/MS/MS. Cationic ST:STUDY_SUMMARY polar metabolites (i.e., amino acids, bases, nucleosides, NAM, SAM, MNAM, SAH, ST:STUDY_SUMMARY me2PY, me4PY, etc) were analyzed via PFPP-LC/HR/MS/MS. ST:INSTITUTE Tohoku University ST:LAST_NAME Kawaoka ST:FIRST_NAME Shinpei ST:ADDRESS 4-1 Seiryo-cho, Sendai, Miyagi, 9808575, Japan ST:EMAIL kawaokashinpei@gmail.com ST:PHONE 0227178568 #SUBJECT SU:SUBJECT_TYPE Mammal SU:SUBJECT_SPECIES Mus musculus SU:TAXONOMY_ID 10090 #SUBJECT_SAMPLE_FACTORS: SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Raw file names and additional sample data SUBJECT_SAMPLE_FACTORS 191015 control_1 Culture conditions:Control | Treatment:No treatment RAW_FILE_NAME=1 SUBJECT_SAMPLE_FACTORS 191015 control_2 Culture conditions:Control | Treatment:No treatment RAW_FILE_NAME=3 SUBJECT_SAMPLE_FACTORS 191015 control_3 Culture conditions:Control | Treatment:No treatment RAW_FILE_NAME=5 SUBJECT_SAMPLE_FACTORS 191015 control_4 Culture conditions:Control | Treatment:No treatment RAW_FILE_NAME=7 SUBJECT_SAMPLE_FACTORS 191015 4T1_1 Culture conditions:4T1-conditioned media | Treatment:No treatment RAW_FILE_NAME=2 SUBJECT_SAMPLE_FACTORS 191015 4T1_2 Culture conditions:4T1-conditioned media | Treatment:No treatment RAW_FILE_NAME=4 SUBJECT_SAMPLE_FACTORS 191015 4T1_3 Culture conditions:4T1-conditioned media | Treatment:No treatment RAW_FILE_NAME=6 SUBJECT_SAMPLE_FACTORS 191015 4T1_4 Culture conditions:4T1-conditioned media | Treatment:No treatment RAW_FILE_NAME=8 SUBJECT_SAMPLE_FACTORS 200401 cont_1 Culture conditions:Control | Treatment:No treatment RAW_FILE_NAME=cell1 SUBJECT_SAMPLE_FACTORS 200401 cont_2 Culture conditions:Control | Treatment:No treatment RAW_FILE_NAME=cell4 SUBJECT_SAMPLE_FACTORS 200401 cont_3 Culture conditions:Control | Treatment:No treatment RAW_FILE_NAME=cell7 SUBJECT_SAMPLE_FACTORS 200401 TNF20_1 Culture conditions:Control | Treatment:TNFalpha (20 ng/mL) treatment RAW_FILE_NAME=cell3 SUBJECT_SAMPLE_FACTORS 200401 TNF20_2 Culture conditions:Control | Treatment:TNFalpha (20 ng/mL) treatment RAW_FILE_NAME=cell6 SUBJECT_SAMPLE_FACTORS 200401 TNF20_3 Culture conditions:Control | Treatment:TNFalpha (20 ng/mL) treatment RAW_FILE_NAME=cell9 SUBJECT_SAMPLE_FACTORS 200401 TNF200_1 Culture conditions:Control | Treatment:TNFalpha (200 ng/mL) treatment RAW_FILE_NAME=cell2 SUBJECT_SAMPLE_FACTORS 200401 TNF200_2 Culture conditions:Control | Treatment:TNFalpha (200 ng/mL) treatment RAW_FILE_NAME=cell5 SUBJECT_SAMPLE_FACTORS 200401 TNF200_3 Culture conditions:Control | Treatment:TNFalpha (200 ng/mL) treatment RAW_FILE_NAME=cell8 #COLLECTION CO:COLLECTION_SUMMARY 4T1 cells were cultured in 10 cm dishes for 48 hours and the culture supernatant CO:COLLECTION_SUMMARY was collected. The supernatant was stored as the 4T1-conditioned media at 4°C CO:COLLECTION_SUMMARY until use. AML cells per a well were cultured in a 6 well plate for 24 hours, CO:COLLECTION_SUMMARY and then the media was switched to the 4T1-conditioned media. After 24 hours, CO:COLLECTION_SUMMARY the treated AML12 cells were collected. CO:SAMPLE_TYPE AML cells #TREATMENT TR:TREATMENT_SUMMARY AML cells per well were cultured in a 24 well plate for 24 hours. The media was TR:TREATMENT_SUMMARY then switched to the bovine-serum free media, and TNF alpha was added at the TR:TREATMENT_SUMMARY concentration of 20 ng/ml or 200 ng/ml (Roche). After 24 hours, the treated TR:TREATMENT_SUMMARY AML12 cells were collected. #SAMPLEPREP SP:SAMPLEPREP_SUMMARY Metabolites were extracted from AML12 cells (less than 6 × 10E5 cells/well (6 SP:SAMPLEPREP_SUMMARY well plate)) using the Bligh and Dyer’s method with some modifications. SP:SAMPLEPREP_SUMMARY Briefly, each sample was mixed with 1 mL of cold methanol containing SP:SAMPLEPREP_SUMMARY 10-camphorsulfonic acid (1.5 nmol) and piperazine-1,4-bis (2-ethanesulfonic SP:SAMPLEPREP_SUMMARY acid) (PIPES, 1.5 nmol) as internal standards for mass spectrometry-based SP:SAMPLEPREP_SUMMARY metabolomic analysis. The samples were vigorously mixed by vortexing for 1 min SP:SAMPLEPREP_SUMMARY followed by 5 min of sonication. The extracts were then centrifuged at 16,000 × SP:SAMPLEPREP_SUMMARY g for 5 min at 4 °C, and the resultant supernatant (400 uL) was collected. SP:SAMPLEPREP_SUMMARY After mixing 400 uL of supernatant with 400 uL of chloroform and 320 uL of SP:SAMPLEPREP_SUMMARY water, the aqueous and organic layers were separated by vortexing and subsequent SP:SAMPLEPREP_SUMMARY centrifugation at 16,000 × g and 4 °C for 5 min. The aqueous (upper) layer SP:SAMPLEPREP_SUMMARY (500 uL) was transferred into a clean tube. After the aqueous layer extracts SP:SAMPLEPREP_SUMMARY were evaporated under vacuum, the dried extracts were stored at −80 °C until SP:SAMPLEPREP_SUMMARY the analysis of hydrophilic metabolites. Prior to analysis, the dried aqueous SP:SAMPLEPREP_SUMMARY layer was reconstituted in 50 uL of water. #CHROMATOGRAPHY CH:CHROMATOGRAPHY_SUMMARY Anionic polar metabolites (i.e., organic acids, sugar phosphates, nucleotides, CH:CHROMATOGRAPHY_SUMMARY etc.) were analyzed via IC/HRMS/MS. CH:CHROMATOGRAPHY_TYPE Other CH:INSTRUMENT_NAME Thermo Dionex ICS-5000+ CH:COLUMN_NAME Dionex IonPac AS11-HC (2 um i.d. × 250 mm, 4 um particle size) #ANALYSIS AN:ANALYSIS_TYPE MS #MS MS:INSTRUMENT_NAME Thermo Q Exactive Orbitrap MS:INSTRUMENT_TYPE Orbitrap MS:MS_TYPE ESI MS:ION_MODE NEGATIVE MS:MS_COMMENTS - #MS_METABOLITE_DATA MS_METABOLITE_DATA:UNITS peak area MS_METABOLITE_DATA_START Samples cont_1 cont_2 cont_3 TNF20_1 TNF20_2 TNF20_3 TNF200_1 TNF200_2 TNF200_3 control_1 control_2 control_3 control_4 4T1_1 4T1_2 4T1_3 4T1_4 Factors Culture conditions:Control | Treatment:No treatment Culture conditions:Control | Treatment:No treatment Culture conditions:Control | Treatment:No treatment Culture conditions:Control | Treatment:TNFalpha (20 ng/mL) treatment Culture conditions:Control | Treatment:TNFalpha (20 ng/mL) treatment Culture conditions:Control | Treatment:TNFalpha (20 ng/mL) treatment Culture conditions:Control | Treatment:TNFalpha (200 ng/mL) treatment Culture conditions:Control | Treatment:TNFalpha (200 ng/mL) treatment Culture conditions:Control | Treatment:TNFalpha (200 ng/mL) treatment Culture conditions:Control | Treatment:No treatment Culture conditions:Control | Treatment:No treatment Culture conditions:Control | Treatment:No treatment Culture conditions:Control | Treatment:No treatment Culture conditions:4T1-conditioned media | Treatment:No treatment Culture conditions:4T1-conditioned media | Treatment:No treatment Culture conditions:4T1-conditioned media | Treatment:No treatment Culture conditions:4T1-conditioned media | Treatment:No treatment 10-Camphorsulfonic acid (IS) 5.E+08 4.E+08 4.E+08 5.E+08 4.E+08 3.E+08 5.E+08 4.E+08 4.E+08 5.E+08 5.E+08 4.E+08 6.E+08 5.E+08 6.E+08 6.E+08 4.E+08 PIPES (IS) 1.E+08 1.E+08 1.E+08 1.E+08 1.E+08 1.E+08 1.E+08 1.E+08 1.E+08 8.E+07 6.E+07 7.E+07 9.E+07 8.E+07 1.E+08 1.E+08 8.E+07 Fum 3.E+07 2.E+07 2.E+07 3.E+07 2.E+07 2.E+07 3.E+07 2.E+07 3.E+07 4.E+07 5.E+07 3.E+07 7.E+07 2.E+07 4.E+07 4.E+07 3.E+07 Uracil 0.E+00 0.E+00 0.E+00 0.E+00 0.E+00 0.E+00 0.E+00 0.E+00 0.E+00 6.E+05 6.E+05 3.E+05 8.E+05 5.E+05 2.E+06 8.E+05 7.E+05 MS_METABOLITE_DATA_END #METABOLITES METABOLITES_START metabolite_name cont_1 cont_2 cont_3 TNF20_1 TNF20_2 TNF20_3 TNF200_1 TNF200_2 TNF200_3 control_1 control_2 control_3 control_4 4T1_1 4T1_2 4T1_3 4T1_4 10-Camphorsulfonic acid (IS) 5.E+08 4.E+08 4.E+08 5.E+08 4.E+08 3.E+08 5.E+08 4.E+08 4.E+08 5.E+08 5.E+08 4.E+08 6.E+08 5.E+08 6.E+08 6.E+08 4.E+08 PIPES (IS) 1.E+08 1.E+08 1.E+08 1.E+08 1.E+08 1.E+08 1.E+08 1.E+08 1.E+08 8.E+07 6.E+07 7.E+07 9.E+07 8.E+07 1.E+08 1.E+08 8.E+07 Fum 3.E+07 2.E+07 2.E+07 3.E+07 2.E+07 2.E+07 3.E+07 2.E+07 3.E+07 4.E+07 5.E+07 3.E+07 7.E+07 2.E+07 4.E+07 4.E+07 3.E+07 Uracil 0.E+00 0.E+00 0.E+00 0.E+00 0.E+00 0.E+00 0.E+00 0.E+00 0.E+00 6.E+05 6.E+05 3.E+05 8.E+05 5.E+05 2.E+06 8.E+05 7.E+05 METABOLITES_END #END