| Literature DB >> 25617365 |
Feng Rao1, Jing Xu1, Chenglai Fu1, Jiyoung Y Cha1, Moataz M Gadalla2, Risheng Xu2, James C Barrow3, Solomon H Snyder4.
Abstract
The inositol pyrophosphates, molecular messengers containing an energetic pyrophosphate bond, impact a wide range of biologic processes. They are generated primarily by a family of three inositol hexakisphosphate kinases (IP6Ks), the principal product of which is diphosphoinositol pentakisphosphate (IP7). We report that IP6K2, via IP7 synthesis, is a major mediator of cancer cell migration and tumor metastasis in cell culture and in intact mice. IP6K2 acts by enhancing cell-matrix adhesion and decreasing cell-cell adhesion. This action is mediated by IP7-elicited nuclear sequestration and inactivation of the tumor suppressor liver kinase B1 (LKB1). Accordingly, inhibitors of IP6K2 offer promise in cancer therapy.Entities:
Keywords: IP6K; LKB1; cell-matrix adhesion; cell–cell adhesion; metastasis
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Year: 2015 PMID: 25617365 PMCID: PMC4330756 DOI: 10.1073/pnas.1424642112
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205