PTEN Overexpression Cooperates With Lithium to Reduce the Malignancy and to Increase Cell Death by Apoptosis via PI3K/Akt Suppression in Colorectal Cancer Cells. Issue 2 (February 2016)

• Record Type: Journal Article
• Authors: de Araujo, Wallace Martins; Robbs, Bruno Kaufmann; Bastos, Lilian G.; de Souza, Waldemir F.; Vidal, Flávia C.B; Viola, João P.B.; Morgado‐Diaz, Jose A.
• Is Part Of: Journal of cellular biochemistry. Volume 117:Issue 2(2016:Feb.)
• Page Start: 458
• Page End: 469
• Publication Date: 2016-02
• Subjects: COLORECTAL CANCER -- PI3K/Akt -- LITHIUM -- PTEN; Cytochemistry -- Periodicals; 572
• DOI: 10.1002/jcb.25294
• Languages: English
• ISSNs: 0730-2312

Abstract

ABSTRACT: Lithium is a well‐established non‐competitive inhibitor of glycogen synthase kinase‐3β (GSK‐3β), a kinase that is involved in several cellular processes related to cancer progression. GSK‐3β is regulated upstream by PI3K/Akt, which is negatively modulated by PTEN. The role that lithium plays in cancer is controversial because lithium can activate or inhibit survival signaling pathways depending on the cell type. In this study, we analyzed the mechanisms by which lithium can modulate events related to colorectal cancer (CRC) progression and evaluated the role that survival signaling pathways such as PI3K/Akt and PTEN play in this context. We show that the administration of lithium decreased the proliferative potential of CRC cells in a GSK‐3β‐independent manner but induced the accumulation of cells in G2/M phase. Furthermore, high doses of lithium increased apoptosis, which was accompanied by decreased proteins levels of Akt and PTEN. Then, cells that were induced to overexpress PTEN were treated with lithium; we observed that low doses of lithium strongly increased apoptosis. Additionally, PTEN overexpression reduced proliferation, but this effect was minor compared with that in cells treated with lithium alone. Furthermore, we demonstrated that PTEN overexpression and lithium treatment separately reduced cell migration, colony formation, and invasion, and these effects were enhanced when lithium treatment and PTEN overexpression were combined. In conclusion, our findings indicate that PTEN overexpression and lithium treatment cooperate to reduce the malignancy of CRC cells and highlight lithium and PTEN as potential candidates for studies to identify new therapeutic approaches for CRC treatment. J. Cell. Biochem. 117: 458–469, 2016. © 2015 Wiley Periodicals, Inc.