Literature DB >> 27278932

Double inhibition of cAMP and mTOR signalling may potentiate the reduction of cell growth in ADPKD cells.

Lucia de Stephanis1, Anna Bonon1, Katia Varani2, Giovanni Lanza3, Roberta Gafà3, Paolo Pinton4, Monika Pema5, Stefan Somlo6, Alessandra Boletta5, Gianluca Aguiari7.   

Abstract

BACKGROUND: ADPKD is a renal pathology caused by mutations of PKD1 and PKD2 genes, which encode for polycystin-1 (PC1) and polycystin-2 (PC2), respectively. PC1 plays an important role regulating several signal transducers, including cAMP and mTOR, which are involved in abnormal cell proliferation of ADPKD cells leading to the development and expansion of kidney cysts that are a typical hallmark of this disease. Therefore, the inhibition of both pathways could potentiate the reduction of cell proliferation enhancing benefits for ADPKD patients.
METHODS: The inhibition of cAMP- and mTOR-related signalling was performed by Cl-IB-MECA, an agonist of A3 receptors, and rapamycin, respectively. Protein kinase activity was evaluated by immunoblot and cell growth was analyzed by direct cell counting.
RESULTS: The activation of A3AR by the specific agonist Cl-IB-MECA causes a marked reduction of CREB, mTOR, and ERK phosphorylation in kidney tissues of Pkd1 flox/-: Ksp-Cre polycystic mice and reduces cell growth in ADPKD cell lines, but not affects the kidney weight. The combined sequential treatment with rapamycin and Cl-IB-MECA in ADPKD cells potentiates the reduction of cell proliferation compared with the individual compound by the inhibition of CREB, mTOR, and ERK kinase activity. Conversely, the simultaneous application of these drugs counteracts their effect on cell growth, because the inhibition of ERK kinase activity is lost.
CONCLUSION: The double treatment with rapamycin and Cl-IB-MECA may have synergistic effects on the inhibition of cell proliferation in ADPKD cells suggesting that combined therapies could improve renal function in ADPKD patients.

Entities:  

Keywords:  ADPKD; CREB; Cell growth; ERK signalling; Sequential double treatment; mTOR

Mesh:

Substances:

Year:  2016        PMID: 27278932      PMCID: PMC5496448          DOI: 10.1007/s10157-016-1289-1

Source DB:  PubMed          Journal:  Clin Exp Nephrol        ISSN: 1342-1751            Impact factor:   2.801


  25 in total

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4.  Sirolimus and kidney growth in autosomal dominant polycystic kidney disease.

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5.  Immortalized epithelial cells from human autosomal dominant polycystic kidney cysts.

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10.  Effect of longacting somatostatin analogue on kidney and cyst growth in autosomal dominant polycystic kidney disease (ALADIN): a randomised, placebo-controlled, multicentre trial.

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5.  Effects of TORC1 Inhibition during the Early and Established Phases of Polycystic Kidney Disease.

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6.  Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease - a case report.

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8.  Combination of curcumin and ginkgolide B inhibits cystogenesis by regulating multiple signaling pathways.

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9.  Engineered Kidney Tubules for Modeling Patient-Specific Diseases and Drug Discovery.

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