J 2018

The metabolomic plasma profile of myeloma patients is considerably different from healthy subjects and reveals potential new therapeutic targets

STEINER, Normann, Udo MULLER, Roman HÁJEK, Sabina ŠEVČÍKOVÁ, Bojana BORJAN et. al.

Základní údaje

Originální název

The metabolomic plasma profile of myeloma patients is considerably different from healthy subjects and reveals potential new therapeutic targets

Autoři

STEINER, Normann (40 Rakousko, garant), Udo MULLER (40 Rakousko), Roman HÁJEK (203 Česká republika), Sabina ŠEVČÍKOVÁ (203 Česká republika, domácí), Bojana BORJAN (40 Rakousko), Karin JOHRER (40 Rakousko), Georg GOBEL (40 Rakousko), Andreas PIRCHER (40 Rakousko) a Eberhard GUNSILIUS (40 Rakousko)

Vydání

Plos one, San Francisco, Public Library of Science, 2018, 1932-6203

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30204 Oncology

Stát vydavatele

Spojené státy

Utajení

není předmětem státního či obchodního tajemství

Impakt faktor

Impact factor: 2.776

Kód RIV

RIV/00216224:14110/18:00104193

Organizační jednotka

Lékařská fakulta

UT WoS

000441308500045

Klíčová slova anglicky

Multiple myeloma; monoclonal gammopathy of undetermined significance

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 11. 2. 2019 14:13, Soňa Böhmová

Anotace

V originále

Introduction Multiple myeloma (MM), a malignant plasma cell disorder, is still an incurable disease. Thus, the identification of novel therapeutic targets is of utmost importance. Here, we evaluated the peripheral blood-based metabolic profile of patients with MM. Material & methods Peripheral blood plasma levels of 188 endogenous metabolites, including amino acids, biogenic amines, acylcarnitines, glycerophospholipids, sphingomyelins, and hexoses were determined in patients with plasma cell dyscrasias: monoclonal gammopathy of undetermined significance, a precursor stage of MM (MGUS, n = 15), newly diagnosed MM, (NDMM, n = 32), relapsed/refractory MM (RRMM, n = 19) and in 25 healthy controls by mass spectrometry. Results Patients with NDMM, RRMM and MGUS have a substantially different metabolomic profile than healthy controls. The amount of eight plasma metabolites significantly differs between the NDMM and MGUS group: free carnitine, acetylcarnitine, glutamate, asymmetric dimethylarginine (ADMA) and four phosphatidylcholine (PC) species. In addition, the levels of octadecanoylcarnitine, ADMA and six PCs were significantly different between RRMM and MGUS patients. 13 different concentrations of metabolites were found between RRMM and NDMM patients (free carnitine, acetyicarnitine, creatinine, five LysoPCs and PCs). Pathway analyses revealed a distinct metabolic profile with significant alterations in amino acid, lipid, and energy metabolism in healthy volunteers compared to MGUS/MM patients. Conclusion We identified different metabolic profiles in MGUS und MM patients in comparison to healthy controls. Thus, different metabolic processes, potentially the immunoregulation by indoleamine 2,3 dioxygenase-1 (IDO), which is involved in cancer development and progression supporting inflammatory processes in the tumor microenvironment and glutaminolysis, can serve as novel promising therapeutic targets in MM.