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Oral cancer, one of the six most common human cancers with an overall 5-year survival rate of <50%, is often not diagnosed until it has reached an advanced stage. The aim of the current study is to explore salivary metabolomics as a disease diagnostic and stratification tool for oral cancer and leukoplakia and evaluate the potential of salivary metabolome for detection of oral squamous cell carcinoma (OSCC). Saliva metabolite profiling for a group of 37 OSCC patients, 32 oral leukoplakia (OLK) patients and 34 healthy subjects was performed using ultraperformance liquid chromatography coupled with quadrupole/time-of-flight mass spectrometry in conjunction with multivariate statistical analysis. The OSCC, OLK and healthy control groups demonstrate characteristic salivary metabolic signatures. A panel of five salivary metabolites including c-aminobutyric acid, phenylalanine, valine, n-eicosanoic acid and lactic acid were selected using OPLS-DA model with S-plot. The predictive power of each of the five salivary metabolites was evaluated by receiver operating characteristic curves for OSCC. Valine, lactic acid and phenylalanine in combination yielded satisfactory accuracy (0.89, 0.97), sensitivity (86.5% and 94.6%), specificity (82.4% and 84.4%) and positive predictive value (81.6% and 87.5%) in distinguishing OSCC from the controls or OLK, respectively. The utility of salivary metabolome diagnostics for oral cancer is successfully demonstrated in this study and these results suggest that metabolomics approach complements the clinical detection of OSCC and stratifies the two types of lesions, leading to an improved disease diagnosis and prognosis. About 1.5 million new cancer cases are expected to be diagnosed in 2009 in the United States and >0.5 million Americans are expected to die of cancer this year, averaging about 1,500 deaths per day.1 These numbers have been steadily increasing over the past 15 years, despite significant progress in cancer treatment. Oral cancer represents one of the six most common human cancers with a high morbidity rate and an overall 5-year survival rate of <50%.2,3 Reports indicate an increasing worldwide incidence of oral cancer at an earlier age.4-6 Over 90% of oral cancer is oral squamous cell carcinoma (OSCC) which arises from the oral mucosal lining.7 A critical factor in the lack of prognostic improvement is the fact that a significant proportion of cancers initially are asymptomatic lesions and are not diagnosed or treated until Key words: metabolomics, saliva, oral squamous cell carcinoma, ultraperformance liquid chromatography quadrupole-time of flight mass spectrometry, multivariate statistical analysis, receiver operating characteristics Abbreviations:: OSCC: oral squamous cell carcinoma; OLK: oral leukoplakia; UPLC-QTOFMS: ultraperformance liquid chromatographyquadrupole/time-of-flight mass spectrometry; PCA: principal component analysis; OPLS-DA: orthogonal partial least squares-discriminant analysis; ROC: receiver operating characteristic; LR: logistic regression; VIP: va...
Oral cancer, one of the six most common human cancers with an overall 5-year survival rate of <50%, is often not diagnosed until it has reached an advanced stage. The aim of the current study is to explore salivary metabolomics as a disease diagnostic and stratification tool for oral cancer and leukoplakia and evaluate the potential of salivary metabolome for detection of oral squamous cell carcinoma (OSCC). Saliva metabolite profiling for a group of 37 OSCC patients, 32 oral leukoplakia (OLK) patients and 34 healthy subjects was performed using ultraperformance liquid chromatography coupled with quadrupole/time-of-flight mass spectrometry in conjunction with multivariate statistical analysis. The OSCC, OLK and healthy control groups demonstrate characteristic salivary metabolic signatures. A panel of five salivary metabolites including c-aminobutyric acid, phenylalanine, valine, n-eicosanoic acid and lactic acid were selected using OPLS-DA model with S-plot. The predictive power of each of the five salivary metabolites was evaluated by receiver operating characteristic curves for OSCC. Valine, lactic acid and phenylalanine in combination yielded satisfactory accuracy (0.89, 0.97), sensitivity (86.5% and 94.6%), specificity (82.4% and 84.4%) and positive predictive value (81.6% and 87.5%) in distinguishing OSCC from the controls or OLK, respectively. The utility of salivary metabolome diagnostics for oral cancer is successfully demonstrated in this study and these results suggest that metabolomics approach complements the clinical detection of OSCC and stratifies the two types of lesions, leading to an improved disease diagnosis and prognosis. About 1.5 million new cancer cases are expected to be diagnosed in 2009 in the United States and >0.5 million Americans are expected to die of cancer this year, averaging about 1,500 deaths per day.1 These numbers have been steadily increasing over the past 15 years, despite significant progress in cancer treatment. Oral cancer represents one of the six most common human cancers with a high morbidity rate and an overall 5-year survival rate of <50%.2,3 Reports indicate an increasing worldwide incidence of oral cancer at an earlier age.4-6 Over 90% of oral cancer is oral squamous cell carcinoma (OSCC) which arises from the oral mucosal lining.7 A critical factor in the lack of prognostic improvement is the fact that a significant proportion of cancers initially are asymptomatic lesions and are not diagnosed or treated until Key words: metabolomics, saliva, oral squamous cell carcinoma, ultraperformance liquid chromatography quadrupole-time of flight mass spectrometry, multivariate statistical analysis, receiver operating characteristics Abbreviations:: OSCC: oral squamous cell carcinoma; OLK: oral leukoplakia; UPLC-QTOFMS: ultraperformance liquid chromatographyquadrupole/time-of-flight mass spectrometry; PCA: principal component analysis; OPLS-DA: orthogonal partial least squares-discriminant analysis; ROC: receiver operating characteristic; LR: logistic regression; VIP: va...
Oral cancer typically develops from hyperplasia through dysplasia to carcinoma with a multistep process of carcinogenesis involving genetic alterations resulting in aberrant cellular appearance, deregulated cell growth, and carcinoma. The metabolic transformation during the process of oral carcinogenesis and its implications for cancer therapy have not been extensively investigated. Here, we report a metabonomic study on a classical model of 7,12-dimethylbenz(a)anthracene (DMBA)-induced oral carcinogenesis in hamsters to delineate characteristic metabolic transformation during the carcinogenesis using gas chromatography time-of-flight mass spectrometry (GC-TOF MS). Salvianolic acid B (Sal-B), isolated from Salvia miltiorrhiza Bge, and Breviscapine, a flavonoid isolated from Herba Erigerontis, were used to treat the hamsters exposed to DMBA to investigate the molecular mechanism of the inhibitory effect of the two agents on oral carcinogenesis. The dynamic changes of serum metabolic profiles indicated that both Sal-B and Breviscapine were able to attenuate DMBA-induced metabolic perturbation, which is consistent with the histopathological findings that Sal-B and Breviscapine significantly decreased the squamous cell carcinoma (SCC) incidence in the two treatment groups. Significant alterations of key metabolic pathways, including elevated glutaminolysis and glycolysis, and decreased cholesterol and myo-inositol metabolism, were observed in the DMBA-induced model group, which were attenuated or normalized by Sal-B or Breviscapine treatment. Elevated inflammation and tumor angiogenesis at gene and metabolite expression levels were also observed in DMBA-induced oral dysplasia and SCC but were attenuated or normalized by Sal-B and Breviscapine along with significantly decreased incidences of SCC formation.
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