TY - JOUR
T1 - A new method for investigating microbiota-produced small molecules in adenomatous polyps
AU - Barberis, Elettra
AU - Joseph, Soni
AU - Amede, Elia
AU - Clavenna, Michela Giulia
AU - La Vecchia, Marta
AU - Sculco, Marika
AU - Aspesi, Anna
AU - Occhipinti, Pietro
AU - Robotti, Elisa
AU - Boldorini, Renzo
AU - Marengo, Emilio
AU - Dianzani, Irma
AU - Manfredi, Marcello
N1 - Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/9/22
Y1 - 2021/9/22
N2 - The intestinal microbiota is composed of a large number of different bacteria that produce a variety of metabolites. Colorectal cancer, which typically develops from adenomatous polyps, is highly influenced by microbiota. Since a variety of molecular changes may occur as these polyps transform from benign tumor to malignant carcinoma, the ability to study the microbiota-produced metabolites can lead to new discoveries about the development and progression of this cancer. However, to address the complexity of the microbiota-produced molecules, novel methods are needed. To this aim, in the present work, we developed a high-throughput metabolomics method to capture the metabolic complexity of the microbiota metabolome adherent to adenomatous polyps and adenocarcinoma. For the first time, the method enables the simultaneous quantification of almost 300 metabolites, while preserving the integrity of the original sample. The metabolomics approach was analytically validated and had excellent performances in terms of recovery, linearity, specificity, intra- and inter-day precision, limits of detection, and quantification. Furthermore, the clinical potential of the method was demonstrated in adenoma collected for a colorectal adenoma study.
AB - The intestinal microbiota is composed of a large number of different bacteria that produce a variety of metabolites. Colorectal cancer, which typically develops from adenomatous polyps, is highly influenced by microbiota. Since a variety of molecular changes may occur as these polyps transform from benign tumor to malignant carcinoma, the ability to study the microbiota-produced metabolites can lead to new discoveries about the development and progression of this cancer. However, to address the complexity of the microbiota-produced molecules, novel methods are needed. To this aim, in the present work, we developed a high-throughput metabolomics method to capture the metabolic complexity of the microbiota metabolome adherent to adenomatous polyps and adenocarcinoma. For the first time, the method enables the simultaneous quantification of almost 300 metabolites, while preserving the integrity of the original sample. The metabolomics approach was analytically validated and had excellent performances in terms of recovery, linearity, specificity, intra- and inter-day precision, limits of detection, and quantification. Furthermore, the clinical potential of the method was demonstrated in adenoma collected for a colorectal adenoma study.
KW - Colorectal cancer
KW - Metabolomics
KW - Microbiome
KW - Microbiota-derived metabolome
KW - Non-invasive
UR - https://www.scopus.com/pages/publications/85110212097
U2 - 10.1016/j.aca.2021.338841
DO - 10.1016/j.aca.2021.338841
M3 - Article
SN - 0003-2670
VL - 1179
JO - Analytica Chimica Acta
JF - Analytica Chimica Acta
M1 - 338841
ER -