PIKfyve, MTMR3 and their product PtdIns5P regulate cancer cell migration and invasion through activation of Rac1.

Publisher: Published by Portland Press on behalf of the Biochemical Society Country of Publication: England NLM ID: 2984726R Publication Model: Print Cited Medium: Internet ISSN: 1470-8728 (Electronic) Linking ISSN: 02646021 NLM ISO Abbreviation: Biochem J Subsets: MEDLINE

Original Publication: London, UK : Published by Portland Press on behalf of the Biochemical Society

Carcinoma/*metabolism ; Neoplasm Proteins/*metabolism ; Phosphatidylinositol 3-Kinases/*metabolism ; Phosphatidylinositol Phosphates/*metabolism ; Protein Tyrosine Phosphatases, Non-Receptor/*metabolism ; Sarcoma/*metabolism ; rac1 GTP-Binding Protein/*agonists; Carcinoma/drug therapy ; Carcinoma/pathology ; Cell Line ; Cell Line, Tumor ; Cell Movement/drug effects ; Cell Polarity ; Computational Biology ; Databases, Genetic ; Enzyme Activation/drug effects ; Enzyme Inhibitors/pharmacology ; Expert Systems ; Gene Expression Regulation, Neoplastic ; Humans ; Neoplasm Invasiveness ; Neoplasm Proteins/agonists ; Neoplasm Proteins/antagonists & inhibitors ; Neoplasm Proteins/genetics ; Phosphatidylinositol 3-Kinases/genetics ; Phosphoinositide-3 Kinase Inhibitors ; Protein Tyrosine Phosphatases, Non-Receptor/antagonists & inhibitors ; Protein Tyrosine Phosphatases, Non-Receptor/genetics ; RNA Interference ; Sarcoma/drug therapy ; Sarcoma/pathology ; Software ; rac1 GTP-Binding Protein/metabolism

Previously, we have shown that the phosphoinositide metabolizing enzymes PIKfyve (phosphoinositide 5-kinase, FYVE finger containing) and MTMR3 (myotubularin-related protein 3), together with their lipid product PtdIns5P, are important for migration of normal human fibroblasts. As these proteins are a kinase and a phosphatase respectively, and thereby considered druggable, we wanted to test their involvement in cancer cell migration and invasion. First, we showed that PIKfyve and MTMR3 are expressed in most cancer cells. Next, we demonstrated that depletion of PIKfyve or MTMR3 resulted in decreased velocity in three different cancer cell lines by using new software for cell tracking. Inhibition of the enzymatic activity of PIKfyve by the inhibitor YM201636 also led to a strong reduction in cell velocity. Mechanistically, we show that PIKfyve and MTMR3 regulate the activation of the Rho family GTPase Rac1. Further experiments also implicated PtdIns5P in the activation of Rac1. The results suggest a model for the activation of Rac1 in cell migration where PIKfyve and MTMR3 produce PtdIns5P on cellular membranes which may then serve to recruit effectors to activate Rac1. Finally, in an invasion assay, we demonstrate that both PIKfyve and MTMR3 are implicated in invasive behaviour of cancer cells. Thus PIKfyve and MTMR3 could represent novel therapeutic targets in metastatic cancer.

0 (Enzyme Inhibitors)
0 (Neoplasm Proteins)
0 (Phosphatidylinositol Phosphates)
0 (Phosphoinositide-3 Kinase Inhibitors)
0 (RAC1 protein, human)
0 (phosphatidylinositol 5-phosphate)
EC 2.7.1.137 (PIKFYVE protein, human)
EC 3.1.3.48 (MTMR3 protein, human)
EC 3.1.3.48 (Protein Tyrosine Phosphatases, Non-Receptor)
EC 3.6.5.2 (rac1 GTP-Binding Protein)

Date Created: 20140521 Date Completed: 20140921 Latest Revision: 20191210

20231215

10.1042/BJ20140132

24840251