MALDI Mass Spectrometry Imaging Highlights Specific Metabolome and Lipidome Profiles in Salivary Gland Tumor Tissues

被引:14
作者
Sommella, Eduardo [1 ]
Salviati, Emanuela [1 ]
Caponigro, Vicky [1 ]
Grimaldi, Manuela [1 ]
Musella, Simona [1 ]
Bertamino, Alessia [1 ]
Cacace, Luigi [2 ]
Palladino, Remo [2 ]
Di Mauro, Giuseppe [2 ]
Marini, Federico [3 ]
D'Ursi, Anna Maria [1 ]
Campiglia, Pietro [1 ]
机构
[1] Univ Salerno, Dept Pharm, Via Giovanni Paolo II 132, I-84084 Fisciano, Italy
[2] UOC Clin Pathol DEA III Umberto I, Viale S Francesco DAssisi, I-84014 Nocera Inferiore, Italy
[3] Univ Roma La Sapienza, Dept Chem, Piazzale Aldo Moro 5, I-00185 Rome, Italy
关键词
mass spectrometry imaging; MALDI-MSI; metabolomics; lipidomics; parotid tumor; spatial segmentation; SPATIAL SEGMENTATION; CANCER;
D O I
10.3390/metabo12060530
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Salivary gland tumors are relatively uncommon neoplasms that represent less than 5% of head and neck tumors, and about 90% are in the parotid gland. The wide variety of histologies and tumor characteristics makes diagnosis and treatment challenging. In the present study, Matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) was used to discriminate the pathological regions of patient-derived biopsies of parotid neoplasms by metabolomic and lipidomic profiles. Fresh frozen parotid tissues were analyzed by MALDI time-of-flight (TOF) MSI, both in positive and negative ionization modes, and additional MALDI-Fourier-transform ion cyclotron resonance (FT-ICR) MSI was carried out for metabolite annotation. MALDI-TOF-MSI spatial segmentation maps with different molecular signatures were compared with the histologic annotation. To maximize the information related to specific alterations between the pathological and healthy tissues, unsupervised (principal component analysis, PCA) and supervised (partial least squares-discriminant analysis, PLS-DA) multivariate analyses were performed presenting a 95.00% accuracy in cross-validation. Glycerophospholipids significantly increased in tumor tissues, while sphin-gomyelins and triacylglycerols, key players in the signaling pathway and energy production, were sensibly reduced. In addition, a significant increase of amino acids and nucleotide intermediates, consistent with the bioenergetics request of tumor cells, was observed. These results underline the potential of MALDI-MSI as a complementary diagnostic tool to improve the specificity of diagnosis and monitoring of pharmacological therapies.
引用
收藏
页数:18
相关论文
共 56 条
[1]   Efficient spatial segmentation of large imaging mass spectrometry datasets with spatially aware clustering [J].
Alexandrov, Theodore ;
Kobarg, Jan Hendrik .
BIOINFORMATICS, 2011, 27 (13) :I230-I238
[2]   Spatial Segmentation of Imaging Mass Spectrometry Data with Edge-Preserving Image Denoising and Clustering [J].
Alexandrov, Theodore ;
Becker, Michael ;
Deininger, Soren-Oliver ;
Ernst, Gunther ;
Wehder, Liane ;
Grasmair, Markus ;
von Eggeling, Ferdinand ;
Thiele, Herbert ;
Maass, Peter .
JOURNAL OF PROTEOME RESEARCH, 2010, 9 (12) :6535-6546
[3]  
Ali Naeem Sultan, 2011, ISRN Surg, V2011, P721525, DOI 10.5402/2011/721525
[4]   Spatial differentiation of metabolism in prostate cancer tissue by MALDI-TOF MSI [J].
Andersen, Maria K. ;
Hoiem, Therese S. ;
Claes, Britt S. R. ;
Balluff, Benjamin ;
Martin-Lorenzo, Marta ;
Richardsen, Elin ;
Krossa, Sebastian ;
Bertilsson, Helena ;
Heeren, Ron M. A. ;
Rye, Morten B. ;
Giskeodegard, Guro F. ;
Bathen, Tone F. ;
Tessem, May-Britt .
CANCER & METABOLISM, 2021, 9 (01)
[5]   Metabolomics enables precision medicine: "A White Paper, Community Perspective" [J].
Beger, Richard D. ;
Dunn, Warwick ;
Schmidt, Michael A. ;
Gross, Steven S. ;
Kirwan, Jennifer A. ;
Cascante, Marta ;
Brennan, Lorraine ;
Wishart, David S. ;
Oresic, Matej ;
Hankemeier, Thomas ;
Broadhurst, David I. ;
Lane, Andrew N. ;
Suhre, Karsten ;
Kastenmueller, Gabi ;
Sumner, Susan J. ;
Thiele, Ines ;
Fiehn, Oliver ;
Kaddurah-Daouk, Rima .
METABOLOMICS, 2016, 12 (09)
[6]   Lipid metabolic reprogramming in cancer cells [J].
Beloribi-Djefaflia, S. ;
Vasseur, S. ;
Guillaumond, F. .
ONCOGENESIS, 2016, 5 :e189-e189
[7]   Toward Merging Untargeted and Targeted Methods in Mass Spectrometry-Based Metabolomics and Lipidomics [J].
Cajka, Tomas ;
Fiehn, Oliver .
ANALYTICAL CHEMISTRY, 2016, 88 (01) :524-545
[8]   MALDI-MSI as a Complementary Diagnostic Tool in Cytopathology: A Pilot Study for the Characterization of Thyroid Nodules [J].
Capitoli, Giulia ;
Piga, Isabella ;
Galimberti, Stefania ;
Leni, Davide ;
Pincelli, Angela Ida ;
Garancini, Mattia ;
Clerici, Francesca ;
Mahajneh, Allia ;
Brambilla, Virginia ;
Smith, Andrew ;
Magni, Fulvio ;
Pagni, Fabio .
CANCERS, 2019, 11 (09)
[9]   Metabolomics-assisted discovery of a new anticancer GLS-1 inhibitor chemotype from a nortopsentin-inspired library: From phenotype screening to target identification [J].
Carbone, Daniela ;
Vestuto, Vincenzo ;
Ferraro, Maria Rosalia ;
Ciaglia, Tania ;
Pecoraro, Camilla ;
Sommella, Eduardo ;
Cascioferro, Stella ;
Salviati, Emanuela ;
Novi, Sara ;
Tecce, Mario Felice ;
Amodio, Giuseppina ;
Iraci, Nunzio ;
Cirrincione, Girolamo ;
Campiglia, Pietro ;
Diana, Patrizia ;
Bertamino, Alessia ;
Parrino, Barbara ;
Ostacolo, Carmine .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2022, 234
[10]   Mass spectrometry images acylcarnitines, phosphatidylcholines, and sphingomyelin in MDA-MB-231 breast tumor models [J].
Chughtai, Kamila ;
Jiang, Lu ;
Greenwood, Tiffany R. ;
Glunde, Kristine ;
Heeren, Ron M. A. .
JOURNAL OF LIPID RESEARCH, 2013, 54 (02) :333-344