PIWIL1 is recruited to centrosomes during mitosis in colorectal cancer cells and is linked to cell cycle progression.

Autor: Garcia-Silva MR; Functional Genomics Laboratory, Institut Pasteur Montevideo, Montevideo, Uruguay. rgarcia@pasteur.edu.uy., Montenegro S; Functional Genomics Laboratory, Institut Pasteur Montevideo, Montevideo, Uruguay., Dacosta S; Functional Genomics Laboratory, Institut Pasteur Montevideo, Montevideo, Uruguay., Tosar JP; Functional Genomics Laboratory, Institut Pasteur Montevideo, Montevideo, Uruguay.; Analytical Biochemistry Unit, Nuclear Research Center, Faculty of Science, Universidad de la República, Montevideo, Uruguay., Cayota A; Functional Genomics Laboratory, Institut Pasteur Montevideo, Montevideo, Uruguay.; Departamento Básico de Medicina, Facultad de Medicina, Hospital de Clínicas, Universidad de la República, Montevideo, Uruguay.
Jazyk: angličtina
Zdroj: Scientific reports [Sci Rep] 2024 Oct 13; Vol. 14 (1), pp. 23928. Date of Electronic Publication: 2024 Oct 13.
DOI: 10.1038/s41598-024-75098-6
Abstrakt: PIWI proteins, traditionally associated with germline development, have recently gained attention for their expression in various cancers, including colorectal cancer. However, the molecular mechanisms underlying their reactivation and impact on cancer initiation and progression remain elusive. Here, we found that PIWIL1 is expressed at relatively high levels in CRC-derived samples and cell lines, where it undergoes a dynamic relocalization to the centrosome during mitosis. Knockdown of PIWIL1 induces G2/M arrest associated with disruption of the mitotic spindle and aberrant metaphase events, highlighting its role in cell cycle progression. We also found that the expression of PIWIL1 is lost during the differentiation of Caco-2 cells into enterocytes and that PIWIL1 is expressed in cells at the base of the intestinal crypts in normal human colon tissue, where intestinal stem cells are known to reside. Thus, it is possible that the presence of PIWIL1 in cancer cells reflects a physiological role of this protein in stem cell maintenance, which would argue in favor of the proposed stem cell origin of CRC. Supporting this view, dedifferentiation of human fibroblasts into induced pluripotent stem cells (iPSCs) involves the reactivation of PIWIL2 expression, another member of the PIWI protein family. Overall, our findings suggest a role of PIWIL1 in mediating cell cycle dynamics, both in colorectal cancer cells and possibly also in intestinal stem cells. In a broader aspect, we provide evidence supporting an involvement of PIWI proteins in somatic stem cell maintenance, thus expanding the known non-gonadal functions of this protein family.
(© 2024. The Author(s).)
Databáze: MEDLINE
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