Evidence map›Paper›PMID 24115212›Full record

ArticleMolecular carcinogenesis2015

Cyclic AMP regulates the migration and invasion potential of human pancreatic cancer cells.

Noah P Zimmerman, Ishan Roy, Andrew D Hauser, Jessica M Wilson, Carol L Williams, Michael B Dwinell

Open access · bronzeAbstract read
In one paragraph

Article in Molecular carcinogenesis, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.2field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
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  6. Kisspeptin/KISS1R Signaling Modulates Human Airway Smooth Muscle Cell Migration.American journal of respiratory cell and molecular biology · 2024
    Article
  7. Review
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  17. The Role of PDE8 in T Cell Recruitment and Function in Inflammation.Frontiers in cell and developmental biology · 2021
    Review
  18. Review
  19. Regulating cellular cyclic adenosine monophosphate: "Sources," "sinks," and now, "tunable valves".Wiley interdisciplinary reviews. Systems biology and medicine · 2020
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Noah P ZimmermanDepartment of Microbiology and Molecular Genetics, The Medical College of Wisconsin Cancer Center, 8701 Watertown Plank Road, Milwaukee, Wisconsin, 53226.
Ishan Roy
Andrew D Hauser
Jessica M Wilson
Carol L Williams
Michael B Dwinell
Medical College of Wisconsin · USMedical College of Wisconsin Cancer Center

Funding

Medical Scientist Training ProgramT32GM080202 · NIGMS · MEDICAL COLLEGE OF WISCONSIN · PI BARBIERI, JOSEPH T, SALZMAN, NITA H · 2010 to 2024
$5.7M
Regulation of Ras and Rho Family GTPases in Lung CancerR01CA136799 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI WILLIAMS, CAROL LUCILLE · 2010 to 2014
$1.5M
NCI NIH HHS R01 CA136799NIGMS NIH HHS T32 GM080202
6 · The paper itself

Abstract

Aggressive dissemination and metastasis of pancreatic ductal adenocarcinoma (PDAC) results in poor prognosis and marked lethality. Rho monomeric G protein levels are increased in pancreatic cancer tissue. As the mechanisms underlying PDAC malignancy are little understood, we investigated the role for cAMP in regulating monomeric G protein regulated invasion and migration of pancreatic cancer cells. Treatment of PDAC cells with cAMP elevating agents that activate adenylyl cyclases, forskolin, protein kinase A (PKA), 6-Bnz-cAMP, or the cyclic nucleotide phosphodiesterase inhibitor cilostamide significantly decreased migration and Matrigel invasion of PDAC cell lines. Inhibition was dose-dependent and not significantly different between forskolin or cilostamide treatment. cAMP elevating drugs not only blocked basal migration, but similarly abrogated transforming-growth factor-β-directed PDAC cell migration and invasion. The inhibitory effects of cAMP were prevented by the pharmacological blockade of PKA. Drugs that increase cellular cAMP levels decreased levels of active RhoA or RhoC, with a concomitant increase in phosphorylated RhoA. Diminished Rho signaling was correlated with the appearance of thickened cortical actin bands along the perimeter of non-motile forskolin or cilostamide-treated cells. Decreased migration did not reflect alterations in cell growth or programmed cell death. Collectively these data support the notion that increased levels of cAMP specifically hinder PDAC cell motility through F-actin remodeling.

Indexed as

1-Methyl-3-isobutylxanthineAmidesApoptosisCarcinoma, Pancreatic DuctalCell Line, TumorCell MovementCell ProliferationColforsinCyclic AMPCyclic AMP-Dependent Protein KinasesDeoxycytidineEnzyme InhibitorsGemcitabineHumansNeoplasm InvasivenessPancreatic Neoplasms1-Methyl-3-isobutylxanthineAmidescilostamideColforsinCyclic AMPCyclic AMP-Dependent Protein KinasesDeoxycytidineEnzyme InhibitorsGemcitabinePhosphodiesterase InhibitorsPyridinesQuinolonesrhoA GTP-Binding ProteinrhoC GTP-Binding ProteinRHOC protein, humanrho GTP-Binding ProteinsVasodilator AgentsY 27632carcinoma metastasispancreasphosphodiesteraseprotein kinase ARho

Identifiers

PMID24115212
PMCPMC4087083
OpenAlexW1945691413

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.