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Decoding chromosomal instability insights in CRC by integrating omics and patient-derived organoids

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Autores de INCLIVA

Participantes ajenos a INCLIVA

  • Papaccio, F
  • Gutiérrez-Bravo, MF
  • del Pino, MMS

Grupos y Plataformas de I+D+i

Abstract

BackgroundChromosomal instability (CIN) is involved in about 70% of colorectal cancers (CRCs) and is associated with poor prognosis and drug resistance. From a clinical perspective, a better knowledge of these tumour's biology will help to guide therapeutic strategies more effectively.MethodsWe used high-density chromosomal microarray analysis to evaluate CIN level of patient-derived organoids (PDOs) and their original mCRC tissues. We integrated the RNA-seq and mass spectrometry-based proteomics data from PDOs in a functional interaction network to identify the significantly dysregulated processes in CIN. This was followed by a proteome-wGII Pearson correlation analysis and an in silico validation of main findings using functional genomic databases and patient-tissues datasets to prioritize the high-confidence CIN features.ResultsBy applying the weighted Genome Instability Index (wGII) to identify CIN, we classified PDOs and demonstrated a good correlation with tissues. Multi-omics analysis showed that our organoids recapitulated genomic, transcriptomic and proteomic CIN features of independent tissues cohorts. Thanks to proteotranscriptomics, we uncovered significant associations between mitochondrial metabolism and epithelial-mesenchymal transition in CIN CRC PDOs. Correlating PDOs wGII with protein abundance, we identified a subset of proteins significantly correlated with CIN. Co-localisation analysis in PDOs strengthened the putative role of IPO7 and YAP, and, through in silico analysis, we found that some of the targets give significant dependencies in cell lines with CIN compatible status.ConclusionsWe first demonstrated that PDO models are a faithful reflection of CIN tissues at the genetic and phenotypic level. Our new findings prioritize a subset of genes and molecular processes putatively required to cope with the burden on cellular fitness imposed by CIN and associated with disease aggressiveness.

Datos de la publicación

ISSN/ISSNe:
0392-9078, 1756-9966

JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH  BioMed Central

Tipo:
Article
Páginas:
77-77
PubMed:
40022181

Citas Recibidas en Web of Science: 2

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Keywords

  • Chromosomal instability; Colorectal cancer; Multi-omics; Mass spectrometry-based proteomics; Patient-derived organoids

Campos de Estudio

Financiación

INSTITUTO SALUD CARLOS III (PT20/00029)
Precision Medicine Unit

Proyectos y Estudios Clínicos

Unidad de biobancos y biomodelos de INCLIVA.

Investigador Principal: ANTONIO FERRANDEZ IZQUIERDO

PT20/00029 . INSTITUTO SALUD CARLOS III . 2021

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