Serum Metabolomic Profiles for Breast Cancer Diagnosis, Grading and Staging by Gas Chromatography-Mass Spectrometry

被引:55
作者
Hadi, Naila Irum [1 ]
Jamal, Qamar [1 ]
Iqbal, Ayesha [2 ]
Shaikh, Fouzia [1 ]
Somroo, Saleem [3 ]
Musharraf, Syed Ghulam [2 ,4 ]
机构
[1] Ziauddin Univ, Dept Pathol, Karachi 75600, Pakistan
[2] Univ Karachi, Int Ctr Chem & Biol Sci, Dr Panjwani Ctr Mol Med & Drug Res, Karachi 75270, Pakistan
[3] Jinnah Postgrad Med Ctr JPMC, Breast Clin, Surg Ward 2, Karachi 75510, Pakistan
[4] Univ Karachi, HEJ Res Inst Chem, Int, Ctr Chem & Biol Sci, Karachi 75270, Pakistan
关键词
CLINICAL ONCOLOGY/COLLEGE; NEOADJUVANT CHEMOTHERAPY; PREDICTING RESPONSE; AMERICAN SOCIETY; LIPID-METABOLISM; RECEPTOR STATUS; PHOSPHORYLATION; RECOMMENDATIONS; BIOMARKERS; SURVIVAL;
D O I
10.1038/s41598-017-01924-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Detection of metabolic signature for breast cancer (BC) has the potential to improve patient prognosis. This study identified potentially significant metabolites differentiating between breast cancer patients and healthy controls to help in diagnosis, grading, staging and determination of neoadjuvant status. Serum was collected from 152 pre-operative breast cancer (BC) patients and 155 healthy controls in this case-controlled study. Gas chromatography-mass spectrometry (GC-MS) was used to obtain metabolic profiles followed by chemometric analysis with the identification of significantly differentiated metabolites including 7 for diagnosis, 18 for grading, 23 for staging, 15 for stage III subcategory and 10 for neoadjuvant status (p-value < 0.05). Partial Least Square Discriminant Analysis (PLS-DA) model revealed a distinct separation between healthy controls and BC patients with a sensitivity of 96% and specificity of 100% on external validation. Models for grading, staging and neoadjuvant status were built with Decision Tree Algorithm with predictive accuracy of 71.5%, 71.3% and 79.8% respectively. Pathway analysis revealed increased glycolysis, lipogenesis, and production of volatile organic metabolites indicating the metabolic alterations in breast cancer.
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页数:11
相关论文
共 48 条
[31]   Metabolite profiling of human plasma by different extraction methods through gas chromatography-mass spectrometry-An objective comparison [J].
Musharraf, Syed Ghulam ;
Mazhar, Shumaila ;
Siddiqui, Amna Jabbar ;
Choudhary, M. Iqbal ;
Atta-ur-Rahman .
ANALYTICA CHIMICA ACTA, 2013, 804 :180-189
[32]  
Palazoglu M., 2009, METABOLITE IDENTIFIC, P1
[33]   Detection of lung, breast, colorectal, and prostate cancers from exhaled breath using a single array of nanosensors [J].
Peng, G. ;
Hakim, M. ;
Broza, Y. Y. ;
Billan, S. ;
Abdah-Bortnyak, R. ;
Kuten, A. ;
Tisch, U. ;
Haick, H. .
BRITISH JOURNAL OF CANCER, 2010, 103 (04) :542-551
[34]   Effect of age on the breath methylated alkane contour, a display of apparent new markers of oxidative stress [J].
Phillips, M ;
Cataneo, RN ;
Greenberg, J ;
Gunawardena, R ;
Naidu, A ;
Rahbari-Oskoui, F .
JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 2000, 136 (03) :243-249
[35]  
Phillips Michael, 2003, Breast J, V9, P184, DOI 10.1046/j.1524-4741.2003.09309.x
[36]   Volatile biomarkers in the breath of women with breast cancer [J].
Phillips, Michael ;
Cataneo, Renee N. ;
Saunders, Christobel ;
Hope, Peter ;
Schmitt, Peter ;
Wai, James .
JOURNAL OF BREATH RESEARCH, 2010, 4 (02)
[37]   Analyzing the regulation of metabolic pathways in human breast cancer [J].
Schramm, Gunnar ;
Surmann, Eva-Maria ;
Wiesberg, Stefan ;
Oswald, Marcus ;
Reinelt, Gerhard ;
Eils, Roland ;
Koenig, Rainer .
BMC MEDICAL GENOMICS, 2010, 3
[38]   Glucose metabolism and cancer [J].
Shaw, Reuben J. .
CURRENT OPINION IN CELL BIOLOGY, 2006, 18 (06) :598-608
[39]   Solid phase microextraction, mass spectrometry and metabolomic approaches for detection of potential urinary cancer biomarkers-A powerful strategy for breast cancer diagnosis [J].
Silva, Catarina L. ;
Passos, Mario ;
Camara, Jose S. .
TALANTA, 2012, 89 :360-368
[40]   Comparison of HR MAS MR spectroscopic profiles of breast cancer tissue with clinical parameters [J].
Sitter, B ;
Lundgren, S ;
Bathen, TF ;
Halgunset, J ;
Fjosne, HE ;
Gribbestad, IS .
NMR IN BIOMEDICINE, 2006, 19 (01) :30-40