PARP-1 Expression Influences Cancer Stem Cell Phenotype in Colorectal Cancer Depending on p53

Author:

Puentes-Pardo Jose D.12ORCID,Moreno-SanJuan Sara13,Casado Jorge1,Escudero-Feliu Julia1,López-Pérez David12,Sánchez-Uceta Paula1,González-Novoa Paula1,Gálvez Julio124ORCID,Carazo Ángel15,León Josefa16ORCID

Affiliation:

1. Instituto de Investigación Biosanitaria de Granada, ibs.GRANADA, 18012 Granada, Spain

2. Departamento de Farmacología, Facultad de Farmacia, Universidad de Granada, 18011 Granada, Spain

3. Cytometry and Microscopy Research Service, Instituto de Investigación Biosanitaria de Granada, ibs.GRANADA, 18012 Granada, Spain

4. Centro de Investigación Biomédica en Red-Enfermedades Hepáticas y Digestivas (CIBER-ehd), 18011 Granada, Spain

5. Unidad de Gestión de Microbiología, Hospital Universitario San Cecilio de Granada, 18016 Granada, Spain

6. Unidad de Gestión Clínica de Aparato Digestivo, Hospital Universitario San Cecilio de Granada, 18016 Granada, Spain

Abstract

Poly(ADP-ribose) polymerase-1 (PARP-1) is a protein involved in multiple physiological processes. Elevated PARP-1 expression has been found in several tumours, being associated with stemness and tumorigenesis. In colorectal cancer (CRC), some controversy among studies has been described. In this study, we analysed the expression of PARP-1 and cancer stem cell (CSC) markers in CRC patients with different p53 status. In addition, we used an in vitro model to evaluate the influence of PARP-1 in CSC phenotype regarding p53. In CRC patients, PARP-1 expression correlated with the differentiation grade, but this association was only maintained for tumours harbouring wild-type p53. Additionally, in those tumours, PARP-1 and CSC markers were positively correlated. In mutated p53 tumours, no associations were found, but PARP-1 was an independent factor for survival. According to our in vitro model, PARP-1 regulates CSC phenotype depending on p53 status. PARP-1 overexpression in a wild type p53 context increases CSC markers and sphere forming ability. By contrast, those features were reduced in mutated p53 cells. These results could implicate that patients with elevated PARP-1 expression and wild type p53 could benefit from PARP-1 inhibition therapies, meanwhile it could have adverse effects for those carrying mutated p53 tumours.

Funder

Instituto de Salud Carlos III

Nicolás Monardes Program from the Andalusian Health Service

Ministerio de Universidades

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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