Metabolic Profiles are Principally Different between Cancers of the Liver, Pancreas and Breast

被引:25
作者
Budhu, Anuradha [1 ]
Terunuma, Atsushi [2 ]
Zhang, Geng [3 ]
Hussain, S. Perwez [3 ]
Ambs, Stefan [2 ]
Wang, Xin Wei [1 ]
机构
[1] NCI, Liver Carcinogenesis Sect, Ctr Canc Res, Bethesda, MD 20892 USA
[2] NCI, Mol Epidemiol Sect, Ctr Canc Res, Bethesda, MD 20892 USA
[3] NCI, Pancreat Canc Unit, Human Carcinogenesis Lab, Ctr Canc Res, Bethesda, MD 20892 USA
关键词
Breast; Cancer; Liver; Metabolite; Pancreas; UNKNOWN PRIMARY SITE; HEPATOCELLULAR-CARCINOMA; EXPRESSION SIGNATURE; PROGRESSION; PREDICTION; PROGNOSIS; IDENTIFY; TUMORS;
D O I
10.7150/ijbs.9810
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Molecular profiling of primary tumors may facilitate the classification of patients with cancer into more homogenous biological groups to aid clinical management. Metabolomic profiling has been shown to be a powerful tool in characterizing the biological mechanisms underlying a disease but has not been evaluated for its ability to classify cancers by their tissue of origin. Thus, we assessed metabolomic profiling as a novel tool for multiclass cancer characterization. Global metabolic profiling was employed to identify metabolites in paired tumor and non-tumor liver (n=60), breast (n=130) and pancreatic (n=76) tissue specimens. Unsupervised principal component analysis showed that metabolites are principally unique to each tissue and cancer type. Such a difference can also be observed even among early stage cancers, suggesting a significant and unique alteration of global metabolic pathways associated with each cancer type. Our global high-throughput metabolomic profiling study shows that specific biochemical alterations distinguish liver, pancreatic and breast cancer and could be applied as cancer classification tools to differentiate tumors based on tissue of origin.
引用
收藏
页码:966 / 972
页数:7
相关论文
共 21 条
[1]
Management of "unfavourable" carcinoma of unknown primary site: Synthesis of recent literature [J].
Amela, Eric Yaovi ;
Lauridant-Philippin, Geraldine ;
Cousin, Sophie ;
Ryckewaert, Thomas ;
Adenis, Antoine ;
Penel, Nicolas .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2012, 84 (02) :213-223
[2]
A stromal gene signature associated with inflammatory breast cancer [J].
Boersma, Brenda J. ;
Reimers, Mark ;
Yi, Ming ;
Ludwig, Joseph A. ;
Luke, Brain T. ;
Stephens, Robert M. ;
Yfantis, Harry G. ;
Lee, Dong H. ;
Weinstein, John N. ;
Ambs, Stefan .
INTERNATIONAL JOURNAL OF CANCER, 2008, 122 (06) :1324-1332
[3]
Association of breast cancer outcome with status of p53 and MDM2 SNP309 [J].
Boersma, Brenda J. ;
Howe, Tiffany M. ;
Goodman, Julie E. ;
Yfantis, Harry G. ;
Lee, Dong H. ;
Chanock, Stephen J. ;
Ambs, Stefan .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2006, 98 (13) :911-919
[4]
Identification of metastasis-related microRNAs in hepatocellular carcinoma [J].
Budhu, Anuradha ;
Jia, Hu-Liang ;
Forgues, Marshonna ;
Liu, Chang-Gong ;
Goldsteir, David ;
Lam, Amy ;
Zanetti, Krista A. ;
Ye, Qing-Hai ;
Qin, Lun-Yju ;
Croce, Carlo M. ;
Tang, Zhao-You ;
Wang, Xin Wei .
HEPATOLOGY, 2008, 47 (03) :897-907
[5]
Prediction of venous metastases, recurrence, and prognosis in hepatocellular carcinoma based on a unique immune response signature of the liver microenvironment [J].
Budhu, Anuradha ;
Forgues, Marshonna ;
Ye, Qing-Hai ;
Jia, Hu-Liong ;
He, Ping ;
Zanetti, Krista A. ;
Kammula, Udai S. ;
Chen, Yidong ;
Qin, Lun-Xiu ;
Tang, Zhao-You ;
Wang, Xin Wei .
CANCER CELL, 2006, 10 (02) :99-111
[6]
Integrated Metabolite and Gene Expression Profiles Identify Lipid Biomarkers Associated With Progression of Hepatocellular Carcinoma and Patient Outcomes [J].
Budhu, Anuradha ;
Roessler, Stephanie ;
Zhao, Xuelian ;
Yu, Zhipeng ;
Forgues, Marshonna ;
Ji, Junfang ;
Karoly, Edward ;
Qin, Lun-Xiu ;
Ye, Qing-Hai ;
Jia, Hu-Liang ;
Fan, Jia ;
Sun, Hui-Chuan ;
Tang, Zhao-You ;
Wang, Xin Wei .
GASTROENTEROLOGY, 2013, 144 (05) :1066-+
[7]
Gene expression profiling to identify the histogenetic origin of metastatic adenocarcinomas of unknown primary [J].
Horlings, Hugo M. ;
van Laar, Ryan K. ;
Kerst, Jan-Martijn ;
Helgason, Helgi H. ;
Wesseling, Jelle ;
van der Hoeven, Jacobus J. M. ;
Warmoes, Marc O. ;
Floore, Arno ;
Witteveen, Anke ;
Lahti-Domenici, Jaana ;
Glas, Annuska M. ;
Van't Veer, Laura J. ;
de Jong, Daphne .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (27) :4435-4441
[8]
Hudson R.S., 2012, Oncogene
[9]
Expression profiling identifies microRNA signature in pancreatic cancer [J].
Lee, Eun Jon ;
Gusev, Yuriy ;
Jiang, Jinmai ;
Nuovo, Gerard J. ;
Lerner, Megan R. ;
Frankel, Wendy L. ;
Morgan, Daniel L. ;
Postier, Russell G. ;
Brackett, Daniel J. ;
Schmittgen, Thomas D. .
INTERNATIONAL JOURNAL OF CANCER, 2007, 120 (05) :1046-1054
[10]
Epidemiology of unknown primary tumours [J].
Levi, F ;
Te, VC ;
Erler, G ;
Randimbison, L ;
La Vecchia, C .
EUROPEAN JOURNAL OF CANCER, 2002, 38 (13) :1810-1812