#METABOLOMICS WORKBENCH STUDY_ID:ST000276 ANALYSIS_ID:AN000440 PROJECT_ID:PR000154
VERSION             	1
CREATED_ON          	01-15-2019
#PROJECT
PR:PROJECT_TITLE                 	Isocitrate dehydrogenase-1 and Glioma Studies
PR:PROJECT_SUMMARY               	Dr. Stegh will define the role of a novel glioma oncoprotein, termed isocitrate
PR:PROJECT_SUMMARY               	dehydrogenase-1 (IDH1), in driving progression and therapy resistance of
PR:PROJECT_SUMMARY               	glioblastoma (GBM).  Understanding the molecular basis of the therapy
PR:PROJECT_SUMMARY               	refractoriness of GBM is one of the most important areas of glioma research.
PR:PROJECT_SUMMARY               	IDH1 is a critical enzyme of the citric acid cycle (CAC) and is a master
PR:PROJECT_SUMMARY               	regulator of metabolism. Building on his preliminary studies, Dr. Stegh will
PR:PROJECT_SUMMARY               	molecularly characterize the precise mechanism, by which IDH1 protects glioma
PR:PROJECT_SUMMARY               	cells from therapy-induced cell death using glioma cell and mouse models. To
PR:PROJECT_SUMMARY               	target IDH1 signaling in GBM, he will leverage these model systems and
PR:PROJECT_SUMMARY               	mechanistical knowledge to develop and preclinically characterize RNA
PR:PROJECT_SUMMARY               	interference RNAi-based nanomaterials. He will generate RNAi-functionalized
PR:PROJECT_SUMMARY               	spherical nucleic acids (SNAs) that neutralize IDH1 expression in established
PR:PROJECT_SUMMARY               	gliomas. Due to the negative charge of the RNA backbone, however, siRNA
PR:PROJECT_SUMMARY               	oligonucleotides have many downsides, such as they trigger auto-immune
PR:PROJECT_SUMMARY               	responses, and cannot cross the blood-brain-barrier (BBB). In contrast, SNAs are
PR:PROJECT_SUMMARY               	able to transverse cellular membranes, do not require the use of toxic auxiliary
PR:PROJECT_SUMMARY               	reagents, and accumulate in cells and intracranial tumors very effectively. They
PR:PROJECT_SUMMARY               	also exhibit extraordinary stability in physiological environments, cross the
PR:PROJECT_SUMMARY               	BBB, are highly resistant to nuclease degradation, and thus, can move through
PR:PROJECT_SUMMARY               	biological fluids and avoid being destroyed as “foreign materials.” Dr.
PR:PROJECT_SUMMARY               	Stegh proposes to preclinically evaluate these IDH1-targeting nanoconjugates to
PR:PROJECT_SUMMARY               	provide a fundamentally novel treatment option of patients diagnosed with GBM,
PR:PROJECT_SUMMARY               	and will aid in successfully implementing RNAi-based therapies into
PR:PROJECT_SUMMARY               	neuro-oncological practice.
PR:INSTITUTE                     	Northwestern University
PR:DEPARTMENT                    	Neurology
PR:LABORATORY                    	Stegh Lab
PR:LAST_NAME                     	Stegh
PR:FIRST_NAME                    	Alexander
PR:ADDRESS                       	Evanston, IL
PR:EMAIL                         	a-stegh@northwestern.edu
PR:PHONE                         	312-503-2879
PR:DOI                           	http://dx.doi.org/10.21228/M8688J
#STUDY
ST:STUDY_TITLE                   	IDH1 and Glioma knockdown idh1
ST:STUDY_SUMMARY                 	This study is a part of series performed for the same researcher through
ST:STUDY_SUMMARY                 	pilot/feasibility grant program, so the publication is relevant reference for
ST:STUDY_SUMMARY                 	other studies (ST000199)This specific experiment is a pilot study to compare the
ST:STUDY_SUMMARY                 	metabolism of cells transformed using empty vector against cells transformed
ST:STUDY_SUMMARY                 	with vector carrying short hairpin RNA (shRNA) targeted to silence isocitrate
ST:STUDY_SUMMARY                 	dehydrogenase-1 (IDH1) gene.
ST:INSTITUTE                     	University of Michigan
ST:DEPARTMENT                    	Neurology
ST:LABORATORY                    	Stegh Lab (Northwestern University)
ST:LAST_NAME                     	Calvert
ST:FIRST_NAME                    	Andrea
ST:ADDRESS                       	Evanston, IL
ST:EMAIL                         	a-calvert@u.northwestern.edu
ST:PHONE                         	312-503-3134
#SUBJECT
SU:SUBJECT_TYPE                  	Human
SU:SUBJECT_SPECIES               	Homo sapiens
SU:TAXONOMY_ID                   	9606
SU:SPECIES_GROUP                 	Human
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Additional sample data
SUBJECT_SAMPLE_FACTORS           	-	S00014999	IDH1 Knockdown:No	
SUBJECT_SAMPLE_FACTORS           	-	S00015000	IDH1 Knockdown:No	
SUBJECT_SAMPLE_FACTORS           	-	S00015001	IDH1 Knockdown:No	
SUBJECT_SAMPLE_FACTORS           	-	S00015002	IDH1 Knockdown:No	
SUBJECT_SAMPLE_FACTORS           	-	S00015003	IDH1 Knockdown:No	
SUBJECT_SAMPLE_FACTORS           	-	S00015004	IDH1 Knockdown:yes	
SUBJECT_SAMPLE_FACTORS           	-	S00015005	IDH1 Knockdown:yes	
SUBJECT_SAMPLE_FACTORS           	-	S00015006	IDH1 Knockdown:yes	
SUBJECT_SAMPLE_FACTORS           	-	S00015007	IDH1 Knockdown:yes	
SUBJECT_SAMPLE_FACTORS           	-	S00015008	IDH1 Knockdown:yes	
#COLLECTION
CO:SAMPLE_TYPE                   	Cells, Cultured
CO:COLLECTION_SUMMARY            	-
#TREATMENT
TR:TREATMENT_SUMMARY             	-
#SAMPLEPREP
SP:SAMPLEPREP_PROTOCOL_FILENAME  	Gly-TCA-nucleotides_analysis_protocol-2015-03-09.docx
SP:SAMPLEPREP_SUMMARY            	-
#CHROMATOGRAPHY
CH:METHODS_ID                    	AQM020
CH:METHODS_FILENAME              	QTOF-002-HILIC-35min-1mm.m
CH:INSTRUMENT_NAME               	Agilent 1260
CH:COLUMN_NAME                   	Phenomenex Luna NH2 (150 x 1mm, 3um)
CH:CHROMATOGRAPHY_TYPE           	HILIC
#ANALYSIS
AN:LABORATORY_NAME               	MRC2 (University of Michigan)
AN:ANALYSIS_TYPE                 	MS
AN:ACQUISITION_PARAMETERS_FILE   	Column1_solv1_jetstream+_grad9.m
AN:PROCESSING_PARAMETERS_FILE    	EX00317-MassHunterQuant-GlyTCA-DataAnalysis-LCMS-Method.m
#MS
MS:MS_COMMENTS                   	-
MS:INSTRUMENT_NAME               	Agilent 6530 QTOF
MS:INSTRUMENT_TYPE               	QTOF
MS:MS_TYPE                       	ESI
MS:ION_MODE                      	POSITIVE
#MS_METABOLITE_DATA
MS_METABOLITE_DATA:UNITS         	pmol/µg protein
MS_METABOLITE_DATA_START
Samples	S00014999	S00015000	S00015001	S00015002	S00015003	S00015004	S00015005	S00015006	S00015007	S00015008
Factors	IDH1 Knockdown:No	IDH1 Knockdown:No	IDH1 Knockdown:No	IDH1 Knockdown:No	IDH1 Knockdown:No	IDH1 Knockdown:yes	IDH1 Knockdown:yes	IDH1 Knockdown:yes	IDH1 Knockdown:yes	IDH1 Knockdown:yes	
2 or 3-phosphoglycerate_2PG/3PG	15.2684	20.6190	23.4381	12.2102	15.2395	22.2005	15.0676	21.5047	15.1398	16.4459
6-Phosphogluconate	17.6862	23.7846	26.4129	13.7886	19.1897	27.0367	17.7068	27.2094	19.1007	21.8335
Acetyl-CoA	16.8594	22.4543	24.8554	13.1727	16.5836	22.1267	15.1568	22.5592	16.6330	17.4050
ADP	141.8273	180.8952	198.6299	129.0832	98.7574	205.7849	151.8220	236.9052	194.7472	181.0240
AMP	652.5372	829.6242	919.1071	448.6940	428.6916	749.0836	541.5650	735.6193	574.4925	463.0508
ATP	461.9507	470.3373	552.7637	479.1216	262.0738	694.2409	464.7696	870.7787	777.8531	794.8952
Citrate or Isocitrate	936.5463	949.5495	1230.5785	690.9270	821.0633	709.6282	465.9267	727.7756	626.5704	669.6705
erythrose	33.0442	28.7963	77.8063	24.1673	62.2370		7.6639	5.0417	9.2515	26.6524
Erythrose 4-phosphate	35.6925	29.9809	61.1633	29.5472	37.2907	42.0780	29.6363	55.4645	47.4340	45.8037
flavin adenine dinucleotide	7.4979	10.3560	12.1225	6.2196	7.6605	10.3921	7.1655	11.8516	8.7628	9.0587
Fructose 1_6-bisphosphate	69.3080	82.8799	98.7222	57.2519	45.6666	71.5205	60.1630	78.8434	60.9669	61.6814
Glucose 6-phosphate or fructose-6-phosphate	85.1880	75.1851	99.5117	60.8493	57.9876	91.3182	56.2837	114.4483	86.0812	92.1941
guanosine 5^-diphosphate	23.2924	45.0739	47.6427	28.1244	20.4777	44.3769	38.4507	69.3249	48.6709	52.9583
guanosine 5^-monophosphate	3.4553	5.3458	5.6254	3.0489	3.1901	4.5709	3.5829	5.8280	3.8469	3.7847
guanosine 5^-triphosphate	16.5563	26.3197	29.0029	17.4227	18.3531	29.8463	21.6192	38.5941	30.0206	34.9164
Malate	991.9140	907.7035	1279.6747	866.3719	698.6432	1111.6626	699.9722	944.3375	940.4108	902.7140
Nicotinamide Adenine Dinucleotide oxidized	90.7688	93.6636	121.4057	73.7462	63.4411	139.0454	86.6988	145.4194	112.1841	113.1869
nicotinamide adenine dinucleotide phosphate oxidized	4.3046	1.0805	4.2444	2.2002		3.7090	1.4878	5.8322	3.2584	3.2117
nicotinamide adenine dinucleotide phosphate reduced	26.7725	35.0579	36.4935	25.6258	24.2748	33.2817	27.0430	32.3769	31.7478	29.7391
Nicotinamide Adenine Dinucleotide reduced	13.8329	21.1491	23.3243	11.6355	15.8388	19.9616	13.2308	20.6977	13.9447	14.9794
Phosphoenolpyruvate	30.9780	45.3703	49.8261	24.6009	35.2011	46.0490	30.7370		30.9441	
Ribose-5-phosphate or xylulose 5-phosphate	23.7059	14.9983	28.0342	15.1046	11.5529	28.3019	14.9329	24.1783	19.8986	18.4868
sedoheptulose	10.4741	12.7426	15.8358	5.6668	8.5453	10.3963	6.9639	11.3288	8.3560	10.3075
Sedoheptulose 7-phosphate	15.0706	17.8956	23.3110	13.3722	16.0837	23.7804	12.5196	28.5041	19.0734	19.9277
Sucrose	62.3013	85.6996	102.1007	54.5533	62.3990	100.4478	66.7923	89.4629	73.0057	79.7717
MS_METABOLITE_DATA_END
#METABOLITES
METABOLITES_START
metabolite_name	pubchem_id	inchi_key	kegg_id	other_id	other_id_type	ri	ri_type	moverz_quant	
2 or 3-phosphoglycerate_2PG/3PG	724		C00597	2PG/3PG	UM_Target_ID				
6-Phosphogluconate	91493		C00345	6PG	UM_Target_ID				
Acetyl-CoA	444493		C00024	aCoA	UM_Target_ID				
ADP	6022		C00008	ADP	UM_Target_ID				
AMP	6083		C00020	AMP	UM_Target_ID				
ATP	5957		C00002	ATP	UM_Target_ID				
Citrate or Isocitrate	311		C00158	CIT/ICIT	UM_Target_ID				
erythrose	94176		C02143	ERY	UM_Target_ID				
Erythrose 4-phosphate	122357		C00279	E4P	UM_Target_ID				
flavin adenine dinucleotide	643975		C00016	FAD	UM_Target_ID				
Fructose 1,6-bisphosphate	172313		C00354	FBP	UM_Target_ID				
Glucose 6-phosphate or fructose-6-phosphate	5958		C00092	G6P/F6P	UM_Target_ID				
guanosine 5'-diphosphate	8977		C00035	GDP	UM_Target_ID				
guanosine 5'-monophosphate	6804		C00144	GMP	UM_Target_ID				
guanosine 5'-triphosphate	6830		C00044	GTP	UM_Target_ID				
Malate	222656		C00149	MAL	UM_Target_ID				
Nicotinamide Adenine Dinucleotide oxidized	10897651		C00003	NAD	UM_Target_ID				
nicotinamide adenine dinucleotide phosphate oxidized	5886		C00006	NADP	UM_Target_ID				
nicotinamide adenine dinucleotide phosphate reduced	5886		C00006	NADPH	UM_Target_ID				
Nicotinamide Adenine Dinucleotide reduced	439153		C00004	NADH	UM_Target_ID				
Phosphoenolpyruvate	1005		C00074	PEP	UM_Target_ID				
Ribose-5-phosphate or xylulose 5-phosphate	77982		C00117	R5P/X5P	UM_Target_ID				
sedoheptulose	102926			SED	UM_Target_ID				
Sedoheptulose 7-phosphate	165007		C05382	S7P	UM_Target_ID				
Sucrose	5988		C00089	SUC	UM_Target_ID				
METABOLITES_END
#END