Targeting the splicing isoforms of spleen tyrosine kinase affects the viability of colorectal cancer cells.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2022
Historique:
received: 18 03 2022
accepted: 26 08 2022
entrez: 14 9 2022
pubmed: 15 9 2022
medline: 17 9 2022
Statut: epublish

Résumé

Spleen tyrosine kinase (Syk) expression have been both positively and negatively associated with tumorigenesis. Our goal was to evaluate the contribution of Syk and its two splice variants, full length Syk (L) and short isoform Syk (S), in the tumor biology of colorectal cancer cells (CRC). The analysis of Syk expression in primary human colorectal tumors, as well as the analysis of TCGA database, revealed a high Syk mRNA expression score in colorectal cancer tumors, suggesting a tumor promotor role of Syk in CRC. Our analysis showed that Syk (L) isoform is highly expressed in the majority of the tumor tissues and that it remains expressed in tumors in which global Syk expression is downregulated, suggesting the dependence of tumors to Syk (L) isoform. We also identified a small cluster of tumor tissues, which express a high proportion of Syk (S) isoform. This specific cluster is associated with overexpressed genes related to translation and mitochondria, and down regulated genes implicated in the progression of mitosis. For our functional studies, we used short hairpin RNA tools to target the expression of Syk in CRC cells bearing the activating K-Ras (G13D) mutation. Our results showed that while global Syk knock down increases cell proliferation and cell motility, Syk (L) expression silencing affects the viability and induces the apoptosis of the cells, confirming the dependence of cells on Syk (L) isoform for their survival. Finally, we report the promising potential of compound C-13, an original non-enzymatic inhibitor of Syk isolated in our group. In vitro studies showed that C-13 exerts cytotoxic effects on Syk-positive CRC cells by inhibiting their proliferation and their motility, and by inducing their apoptosis, while Syk-negative cell lines viability was not affected. Moreover, the oral and intraperitoneal administration of C-13 reduced the tumor growth of CRC DLD-1 cells xenografts in Nude mice in vivo.

Identifiants

pubmed: 36103569
doi: 10.1371/journal.pone.0274390
pii: PONE-D-22-07966
pmc: PMC9473616
doi:

Substances chimiques

Protein Isoforms 0
Syk Kinase EC 2.7.10.2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0274390

Déclaration de conflit d'intérêts

Piona Dariavach and Pierre Martineau are inventors of the patent application No EP 22306229 “SYK INHIBITORS FOR USE IN THE TREATMENT OF CANCER”. All other authors confirm that they have no competing interests.

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Auteurs

Vincent Denis (V)

IRCM, Univ Montpellier, Inserm, ICM, Montpellier, France.

Nadège Cassagnard (N)

IRCM, Univ Montpellier, Inserm, ICM, Montpellier, France.

Maguy Del Rio (M)

IRCM, Univ Montpellier, Inserm, ICM, Montpellier, France.
Institut régional du Cancer de Montpellier (ICM), Montpellier, France.

Emmanuel Cornillot (E)

IRCM, Univ Montpellier, Inserm, ICM, Montpellier, France.

Nicole Bec (N)

IRCM, Univ Montpellier, Inserm, ICM, Montpellier, France.

Christian Larroque (C)

IRCM, Univ Montpellier, Inserm, ICM, Montpellier, France.

Laura Jeanson (L)

IRCM, Univ Montpellier, Inserm, ICM, Montpellier, France.

Marta Jarlier (M)

Institut régional du Cancer de Montpellier (ICM), Montpellier, France.

Eve Combès (E)

IRCM, Univ Montpellier, Inserm, ICM, Montpellier, France.

Bruno Robert (B)

IRCM, Univ Montpellier, Inserm, ICM, Montpellier, France.

Céline Gongora (C)

IRCM, Univ Montpellier, Inserm, ICM, Montpellier, France.

Pierre Martineau (P)

IRCM, Univ Montpellier, Inserm, ICM, Montpellier, France.

Piona Dariavach (P)

IRCM, Univ Montpellier, Inserm, ICM, Montpellier, France.

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