Summary of Study ST002566

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001653. The data can be accessed directly via it's Project DOI: 10.21228/M81Q6Q This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST002566
Study TitleMetabolomic profiling of PMM2-CDG patient fibroblasts
Study SummaryAbnormal polyol metabolism has been predominantly associated with diabetes, where excess glucose is converted to sorbitol by aldose reductase (AR). Recently, abnormal polyol metabolism has also been implicated in phosphomannomutase 2-congenital disorder of glycosylation (PMM2-CDG), and epalrestat, an AR inhibitor, proposed as a potential therapy for this disorder. Given that the PMM enzyme is not closely connected to polyol metabolism, and, unlike in diabetes, PMM2-CDG does not present with hyperglycemia in blood, the increased polyol production, and the therapeutic mechanism of epalrestat in PMM2-CDG remained largely elusive. PMM2-CDG is caused by deficiency of the PMM enzyme and results in a depletion of mannose-1-P and guanosine diphosphate mannose (GDP-mannose), which is essential for glycosylation. Here, we show that apart from glycosylation abnormalities, PMM2 deficiency also leads to changes in intracellular glucose flux, which results in an increase in intracellular polyols.
Institute
Mayo Clinic
Last NameRadenkovic
First NameSilvia
Address200 2nd Ave SW Rochester MN, USA
Emailradenkovic.silvia@mayo.edu
Phone507(77) 6-6107
Submit Date2023-04-18
Raw Data AvailableYes
Raw Data File Type(s)raw(Thermo)
Analysis Type DetailLC-MS
Release Date2023-07-19
Release Version1
Silvia Radenkovic Silvia Radenkovic
https://dx.doi.org/10.21228/M81Q6Q
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Factors:

Subject type: Cultured cells; Subject species: Homo sapiens (Factor headings shown in green)

mb_sample_id local_sample_id Genotype
SA257951SR02 (9)PMM2-CDG
SA257952SR02 (8)PMM2-CDG
SA257953SR02 (10)PMM2-CDG
SA257954SR02 (11)PMM2-CDG
SA257955SR02 (12)PMM2-CDG
SA257956SR02 (7)PMM2-CDG
SA257957SR02 (6)PMM2-CDG
SA257958SR02 (2)PMM2-CDG
SA257959SR02 (3)PMM2-CDG
SA257960SR02 (4)PMM2-CDG
SA257961SR01 (1)PMM2-CDG
SA257962SR03 (1)PMM2-CDG
SA257963SR03 (2)PMM2-CDG
SA257964SR03 (9)PMM2-CDG
SA257965SR03 (10)PMM2-CDG
SA257966SR03 (11)PMM2-CDG
SA257967SR03 (12)PMM2-CDG
SA257968SR03 (8)PMM2-CDG
SA257969SR03 (7)PMM2-CDG
SA257970SR03 (3)PMM2-CDG
SA257971SR03 (4)PMM2-CDG
SA257972SR03 (5)PMM2-CDG
SA257973SR03 (6)PMM2-CDG
SA257974SR02 (1)PMM2-CDG
SA257975SR02 (5)PMM2-CDG
SA257976SR01 (5)PMM2-CDG
SA257977SR01 (6)PMM2-CDG
SA257978SR01 (15)PMM2-CDG
SA257979SR01 (16)PMM2-CDG
SA257980SR01 (17)PMM2-CDG
SA257981SR01 (7)PMM2-CDG
SA257982SR01 (8)PMM2-CDG
SA257983SR01 (12)PMM2-CDG
SA257984SR01 (14)PMM2-CDG
SA257985SR01 (11)PMM2-CDG
SA257986SR01 (10)PMM2-CDG
SA257987SR01 (9)PMM2-CDG
SA257988SR01 (18)PMM2-CDG
SA257989SR01 (19)PMM2-CDG
SA257990SR01 (13)PMM2-CDG
SA257991SR01 (2)PMM2-CDG
SA257992SR01 (3)PMM2-CDG
SA257993SR01 (20)PMM2-CDG
SA257994SR01 (4)PMM2-CDG
SA257995SR03 (19)WT
SA257996SR03 (20)WT
SA257997SR03 (18)WT
SA257998SR03 (15)WT
SA257999SR03 (13)WT
SA258000SR03 (14)WT
SA258001SR03 (16)WT
SA258002SR03 (17)WT
SA258003SR02 (18)WT
SA258004SR01 (26)WT
SA258005SR01 (25)WT
SA258006SR01 (24)WT
SA258007SR01 (32)WT
SA258008SR01 (31)WT
SA258009SR01 (28)WT
SA258010SR01 (29)WT
SA258011SR01 (30)WT
SA258012SR01 (23)WT
SA258013SR01 (22)WT
SA258014SR02 (17)WT
SA258015SR01 (27)WT
SA258016SR02 (19)WT
SA258017SR02 (16)WT
SA258018SR02 (15)WT
SA258019SR01 (21)WT
SA258020SR02 (13)WT
SA258021SR02 (14)WT
SA258022SR02 (20)WT
Showing results 1 to 72 of 72
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