A convenient and efficient 4-(diethylamino)-butylamine-labeled polarity-response-homodispersed strategy for absolute quantification of carboxyl submetabolome: Monitoring the whole progressive course of hepatocellular carcinoma
•A convenient and efficient workflow for absolute quantification of carboxyl submetabolome was established based on the DEABA-labeled polarity-response-homodispersed strategy.•Carboxyl submetabolome profiling in the whole course of hepatocellular carcinoma was monitored.•Combined with analysis of va...
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Published in | Journal of Chromatography A Vol. 1683; p. 463504 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
08.11.2022
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Subjects | |
Online Access | Get full text |
ISSN | 0021-9673 |
DOI | 10.1016/j.chroma.2022.463504 |
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Abstract | •A convenient and efficient workflow for absolute quantification of carboxyl submetabolome was established based on the DEABA-labeled polarity-response-homodispersed strategy.•Carboxyl submetabolome profiling in the whole course of hepatocellular carcinoma was monitored.•Combined with analysis of variance (ANOVA), orthogonal partial least squares discrimination analysis (OPLS-DA) and Bayesian linear discriminant analysis (BLDA), the biomarkers were screened out and the diagnostic model was established.
Recent studies have shown that dysregulation of carboxyl submetabolome homeostasis is closely related to the occurrence and development of hepatocellular carcinoma (HCC). However, it is still a challenge to quantify carboxyl metabolites with high efficiency by conventional methods due to their species diversity and nature differences. Moreover, there are few studies on carboxyl submetabolome profiling during the whole progression of HCC. In this study, a convenient and efficient workflow for absolute quantification of carboxyl submetabolome was established based on the 4-(diethylamino)-butylamine (DEABA)-labeled polarity-response-homodispersed strategy. After optimizing derivation conditions with response surface methodology (RSM), the reaction only needed 1 min at room temperature, which radically simplified the labeling process. Compared with nonderivatization, the gaps of polarities and responses of the analytes were narrowed by DEABA labeling, realizing the polarity-response-homodispersion. Then resolution and sensitivity in HPLC-MS/MS were improved significantly. Ultimately, the workflow was applied to monitor carboxyl metabolic profile in human plasma of the whole progressive course of hepatocellular carcinoma. Combined with analysis of variance (ANOVA), orthogonal partial least squares discrimination analysis (OPLS-DA), Bayesian linear discriminant analysis (BLDA) and other data mining methods, the biomarkers of “health-hepatitis-cirrhosis-HCC” were screened out, and the diagnostic model was established. Furthermore, the relevancy between carboxyl submetabolome disorders and the pathogenesis of HCC was investigated. The developed method has the characteristics of high sensitivity, high coverage and high practicability, which is suitable for the study of biomarkers of carboxyl submetabolome in the whole progression of HCC.
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AbstractList | Recent studies have shown that dysregulation of carboxyl submetabolome homeostasis is closely related to the occurrence and development of hepatocellular carcinoma (HCC). However, it is still a challenge to quantify carboxyl metabolites with high efficiency by conventional methods due to their species diversity and nature differences. Moreover, there are few studies on carboxyl submetabolome profiling during the whole progression of HCC. In this study, a convenient and efficient workflow for absolute quantification of carboxyl submetabolome was established based on the 4-(diethylamino)-butylamine (DEABA)-labeled polarity-response-homodispersed strategy. After optimizing derivation conditions with response surface methodology (RSM), the reaction only needed 1 min at room temperature, which radically simplified the labeling process. Compared with nonderivatization, the gaps of polarities and responses of the analytes were narrowed by DEABA labeling, realizing the polarity-response-homodispersion. Then resolution and sensitivity in HPLC-MS/MS were improved significantly. Ultimately, the workflow was applied to monitor carboxyl metabolic profile in human plasma of the whole progressive course of hepatocellular carcinoma. Combined with analysis of variance (ANOVA), orthogonal partial least squares discrimination analysis (OPLS-DA), Bayesian linear discriminant analysis (BLDA) and other data mining methods, the biomarkers of “health-hepatitis-cirrhosis-HCC” were screened out, and the diagnostic model was established. Furthermore, the relevancy between carboxyl submetabolome disorders and the pathogenesis of HCC was investigated. The developed method has the characteristics of high sensitivity, high coverage and high practicability, which is suitable for the study of biomarkers of carboxyl submetabolome in the whole progression of HCC. •A convenient and efficient workflow for absolute quantification of carboxyl submetabolome was established based on the DEABA-labeled polarity-response-homodispersed strategy.•Carboxyl submetabolome profiling in the whole course of hepatocellular carcinoma was monitored.•Combined with analysis of variance (ANOVA), orthogonal partial least squares discrimination analysis (OPLS-DA) and Bayesian linear discriminant analysis (BLDA), the biomarkers were screened out and the diagnostic model was established. Recent studies have shown that dysregulation of carboxyl submetabolome homeostasis is closely related to the occurrence and development of hepatocellular carcinoma (HCC). However, it is still a challenge to quantify carboxyl metabolites with high efficiency by conventional methods due to their species diversity and nature differences. Moreover, there are few studies on carboxyl submetabolome profiling during the whole progression of HCC. In this study, a convenient and efficient workflow for absolute quantification of carboxyl submetabolome was established based on the 4-(diethylamino)-butylamine (DEABA)-labeled polarity-response-homodispersed strategy. After optimizing derivation conditions with response surface methodology (RSM), the reaction only needed 1 min at room temperature, which radically simplified the labeling process. Compared with nonderivatization, the gaps of polarities and responses of the analytes were narrowed by DEABA labeling, realizing the polarity-response-homodispersion. Then resolution and sensitivity in HPLC-MS/MS were improved significantly. Ultimately, the workflow was applied to monitor carboxyl metabolic profile in human plasma of the whole progressive course of hepatocellular carcinoma. Combined with analysis of variance (ANOVA), orthogonal partial least squares discrimination analysis (OPLS-DA), Bayesian linear discriminant analysis (BLDA) and other data mining methods, the biomarkers of “health-hepatitis-cirrhosis-HCC” were screened out, and the diagnostic model was established. Furthermore, the relevancy between carboxyl submetabolome disorders and the pathogenesis of HCC was investigated. The developed method has the characteristics of high sensitivity, high coverage and high practicability, which is suitable for the study of biomarkers of carboxyl submetabolome in the whole progression of HCC. [Display omitted] |
ArticleNumber | 463504 |
Author | Zhang, Qian Xing, Luwen Bi, Kaishun Li, Qing Tong, Minghui Zhang, Yiwen |
Author_xml | – sequence: 1 givenname: Minghui surname: Tong fullname: Tong, Minghui – sequence: 2 givenname: Qian surname: Zhang fullname: Zhang, Qian – sequence: 3 givenname: Yiwen surname: Zhang fullname: Zhang, Yiwen – sequence: 4 givenname: Luwen surname: Xing fullname: Xing, Luwen – sequence: 5 givenname: Kaishun surname: Bi fullname: Bi, Kaishun – sequence: 6 givenname: Qing orcidid: 0000-0003-3087-4692 surname: Li fullname: Li, Qing email: lqyxm@hotmail.com |
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Keywords | DEABA LLOQ Hepatocellular carcinoma MRM UDCA Derivatization GCDCA MDCA ANOVA BLDA HOBt FA 20:2-n6 ESI HATU CDCA PGE2 RSD DCA GCA HPLC-MS OPLS-DA HCC GHDCA RSM COX RE HDCA Carboxyl submetabolome |
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Snippet | •A convenient and efficient workflow for absolute quantification of carboxyl submetabolome was established based on the DEABA-labeled... Recent studies have shown that dysregulation of carboxyl submetabolome homeostasis is closely related to the occurrence and development of hepatocellular... |
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SubjectTerms | ambient temperature analysis of variance Bayesian theory biomarkers Carboxyl submetabolome chemical species chromatography Derivatization discriminant analysis Hepatocellular carcinoma hepatoma homeostasis humans metabolites pathogenesis response surface methodology species diversity |
Title | A convenient and efficient 4-(diethylamino)-butylamine-labeled polarity-response-homodispersed strategy for absolute quantification of carboxyl submetabolome: Monitoring the whole progressive course of hepatocellular carcinoma |
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