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Proteins in stool as biomarkers for non-invasive detection of colorectal adenomas with high risk of progression.
Komor, Malgorzata A; Bosch, Linda Jw; Coupé, Veerle Mh; Rausch, Christian; Pham, Thang V; Piersma, Sander R; Mongera, Sandra; Mulder, Chris Jj; Dekker, Evelien; Kuipers, Ernst J; van de Wiel, Mark A; Carvalho, Beatriz; Fijneman, Remond Ja; Jimenez, Connie R; Meijer, Gerrit A; de Wit, Meike.
Afiliación
  • Komor MA; Department of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Bosch LJ; Department of Medical Oncology, Amsterdam UMC, VU University Medical Center, Amsterdam, The Netherlands.
  • Coupé VM; Department of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Rausch C; Department of Epidemiology and Biostatistics, Amsterdam UMC, VU University Medical Center, Amsterdam, The Netherlands.
  • Pham TV; Department of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Piersma SR; Department of Medical Oncology, Amsterdam UMC, VU University Medical Center, Amsterdam, The Netherlands.
  • Mongera S; Department of Medical Oncology, Amsterdam UMC, VU University Medical Center, Amsterdam, The Netherlands.
  • Mulder CJ; Department of Pathology, Amsterdam UMC, VU University Medical Center, Amsterdam, The Netherlands.
  • Dekker E; Department of Gastroenterology and Hepatology, Amsterdam UMC, VU University Medical Center, Amsterdam, The Netherlands.
  • Kuipers EJ; Department of Gastroenterology and Hepatology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • van de Wiel MA; Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
  • Carvalho B; Department of Epidemiology and Biostatistics, Amsterdam UMC, VU University Medical Center, Amsterdam, The Netherlands.
  • Fijneman RJ; Department of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Jimenez CR; Department of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Meijer GA; Department of Medical Oncology, Amsterdam UMC, VU University Medical Center, Amsterdam, The Netherlands.
  • de Wit M; Department of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
J Pathol ; 250(3): 288-298, 2020 03.
Article en En | MEDLINE | ID: mdl-31784980
ABSTRACT
Screening to detect colorectal cancer (CRC) in an early or premalignant state is an effective method to reduce CRC mortality rates. Current stool-based screening tests, e.g. fecal immunochemical test (FIT), have a suboptimal sensitivity for colorectal adenomas and difficulty distinguishing adenomas at high risk of progressing to cancer from those at lower risk. We aimed to identify stool protein biomarker panels that can be used for the early detection of high-risk adenomas and CRC. Proteomics data (LC-MS/MS) were collected on stool samples from adenoma (n = 71) and CRC patients (n = 81) as well as controls (n = 129). Colorectal adenoma tissue samples were characterized by low-coverage whole-genome sequencing to determine their risk of progression based on specific DNA copy number changes. Proteomics data were used for logistic regression modeling to establish protein biomarker panels. In total, 15 of the adenomas (15.8%) were defined as high risk of progressing to cancer. A protein panel, consisting of haptoglobin (Hp), LAMP1, SYNE2, and ANXA6, was identified for the detection of high-risk adenomas (sensitivity of 53% at specificity of 95%). Two panels, one consisting of Hp and LRG1 and one of Hp, LRG1, RBP4, and FN1, were identified for high-risk adenomas and CRCs detection (sensitivity of 66% and 62%, respectively, at specificity of 95%). Validation of Hp as a biomarker for high-risk adenomas and CRCs was performed using an antibody-based assay in FIT samples from a subset of individuals from the discovery series (n = 158) and an independent validation series (n = 795). Hp protein was significantly more abundant in high-risk adenoma FIT samples compared to controls in the discovery (p = 0.036) and the validation series (p = 9e-5). We conclude that Hp, LAMP1, SYNE2, LRG1, RBP4, FN1, and ANXA6 may be of value as stool biomarkers for early detection of high-risk adenomas and CRCs. © 2019 Authors. Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Biomarcadores de Tumor / Adenoma / Detección Precoz del Cáncer / Heces Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Biomarcadores de Tumor / Adenoma / Detección Precoz del Cáncer / Heces Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article