Abstract

Deregulation of intracellular signal transduction pathways is a hallmark of cancer cells, clearly differentiating them from healthy cells. Differential intracellular distribution of the cAMP-dependent protein kinases (PKA) was previously detected in cell cultures and in vivo in glioblastoma and medulloblastoma. Our goal is to extend this observation to meningioma, to explore possible differences among tumors of different origins and prospective outcomes. The distribution of regulatory and catalytic subunits of PKA has been examined in tissue specimens obtained during surgery from meningioma patients. PKA RI subunit appeared more evenly distributed throughout the cytoplasm, but it was clearly detectable only in some tumors. RII was present in discrete spots, presumably at high local concentration; these aggregates could also be visualized under equilibrium binding conditions with fluorescent 8-substituted cAMP analogues, at variance with normal brain tissue and other brain tumors. The PKA catalytic subunit showed exactly overlapping pattern to RII and in fixed sections could be visualized by fluorescent cAMP analogues. Gene expression analysis showed that the PKA catalytic subunit revealed a significant correlation pattern with genes involved in meningioma. Hence, meningioma patients show a distinctive distribution pattern of PKA regulatory and catalytic subunits, different from glioblastoma, medulloblastoma, and healthy brain tissue. These observations raise the possibility of exploiting the PKA intracellular pathway as a diagnostic tool and possible therapeutic interventions.

Highlights

  • Meningiomas comprise the largest number of central nervous system (CNS) tumors, accounting for more than one-third of all CNS tumors, with a female:male ratio of about 2:1 [1]

  • Meningioma specimens were obtained at surgery and were examined via immunofluorescence to reveal the presence of regulatory and catalytic subunits of protein kinases (PKA), followed by equilibrium binding of fluorescently-tagged 8-derivatives of cyclic adenosine-monophosphate (cAMP)

  • The conditions for optimal immunofluorescence were set on frozen samples: a mild fixation followed by permeabilization gave optimal results for PKA catalytic immunofluorescence

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Summary

Introduction

Meningiomas comprise the largest number of central nervous system (CNS) tumors, accounting for more than one-third of all CNS tumors, with a female:male ratio of about 2:1 [1]. Deregulation of signal transduction mechanisms can be detected in almost all tumor cells, and aberrant signal transduction mechanisms involved in cytoskeleton regulation are presumably present in many meningiomas. In this sense, meningiomas may prove to be of interest because of the involvement of Merlin, a protein encoded by the NF2 gene, which is mutated or lost in roughly one half of meningioma patients [3]. Known as schwannomin, is apparently devoid of any catalytic or DNA binding activity, but is presumably involved in cytoskeleton dynamics, by binding actin, Cancers 2019, 11, 1686; doi:10.3390/cancers11111686 www.mdpi.com/journal/cancers

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