Evidence map›Paper›PMID 26065715›Full record

ArticleScientific reports2015

Caveolin-1 is Associated with Tumor Progression and Confers a Multi-Modality Resistance Phenotype in Pancreatic Cancer.

Moumita Chatterjee, Edgar Ben-Josef, Dafydd G Thomas, Meredith A Morgan, Mark M Zalupski, Gazala Khan, Charles Andrew Robinson, Kent A Griffith, Ching-Shih Chen, Thomas Ludwig and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

67 citing papers in PubMed, 102 citations in OpenAlex.

  1. Elevated Expression of Caveolin-1 Reflects a Poor Prognosis in Patients With Primary Central Nervous System Lymphomas.Neuropathology : official journal of the Japanese Society of Neuropathology · 2026
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  15. Endocytosis in cancer and cancer therapy.Nature reviews. Cancer · 2023
    Review
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7 more citing papers are in PubMed but not listed here.

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

13 authors at 6 institutions in 1 country.

Moumita ChatterjeeThe Ohio State University Medical Center, Arthur G. James Comprehensive Cancer Center and Richard J. Solove Research Institute, Columbus, OH 43210.
Edgar Ben-JosefHospital of the University of Pennsylvania, Philadelphia, PA, 19104.
Dafydd G ThomasUniversity of Michigan Medical Center, Ann Arbor, MI, 48109.
Meredith A MorganUniversity of Michigan Medical Center, Ann Arbor, MI, 48109.
Mark M ZalupskiUniversity of Michigan Medical Center, Ann Arbor, MI, 48109.
Gazala KhanHenry Ford Hospital System, West Bloomfield, MI, 48322.
Charles Andrew RobinsonThe Ohio State University Medical Center, Arthur G. James Comprehensive Cancer Center and Richard J. Solove Research Institute, Columbus, OH 43210.
Kent A GriffithUniversity of Michigan Medical Center, Ann Arbor, MI, 48109.
Ching-Shih ChenThe Ohio State University Medical Center, Arthur G. James Comprehensive Cancer Center and Richard J. Solove Research Institute, Columbus, OH 43210.
Thomas LudwigThe Ohio State University Medical Center, Arthur G. James Comprehensive Cancer Center and Richard J. Solove Research Institute, Columbus, OH 43210.
Tanios Bekaii-SaabThe Ohio State University Medical Center, Arthur G. James Comprehensive Cancer Center and Richard J. Solove Research Institute, Columbus, OH 43210.
Arnab ChakravartiThe Ohio State University Medical Center, Arthur G. James Comprehensive Cancer Center and Richard J. Solove Research Institute, Columbus, OH 43210.
Terence M WilliamsThe Ohio State University Medical Center, Arthur G. James Comprehensive Cancer Center and Richard J. Solove Research Institute, Columbus, OH 43210.
The Ohio State University Wexner Medical Center · USUniversity of Michigan–Ann Arbor · USThe Ohio State University · USHenry Ford Hospital · USHospital of the University of Pennsylvania · USThe Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
The Ohio State University Center for Clinical and Translational ScienceKL2TR001068 · NCATS · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2013 to 2017
$2.7M
Selective Sensitization of Pancreatic Cancer to Therapy by Chk1 and PARP1 InhibitR01CA163895 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MORGAN, MEREDITH A · 2012 to 2016
$1.6M
NCATS NIH HHS KL2 TR001068NCATS NIH HHS KL2TR001068NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA163895
6 · The paper itself

Abstract

Caveolin-1 (Cav-1) is a 21 kDa protein enriched in caveolae, and has been implicated in oncogenic cell transformation, tumorigenesis, and metastasis. We explored roles for Cav-1 in pancreatic cancer (PC) prognostication, tumor progression, resistance to therapy, and whether targeted downregulation could lead to therapeutic sensitization. Cav-1 expression was assessed in cell lines, mouse models, and patient samples, and knocked down in order to compare changes in proliferation, invasion, migration, response to chemotherapy and radiation, and tumor growth. We found Cav-1 is overexpressed in human PC cell lines, mouse models, and human pancreatic tumors, and is associated with worse tumor grade and clinical outcomes. In PC cell lines, disruption/depletion of caveolae/Cav-1 reduces proliferation, colony formation, and invasion. Radiation and chemotherapy up-regulate Cav-1 expression, while Cav-1 depletion induces both chemosensitization and radiosensitization through altered apoptotic and DNA repair signaling. In vivo, Cav-1 depletion significantly attenuates tumor initiation and growth. Finally, Cav-1 depletion leads to altered JAK/STAT, JNK, and Src signaling in PC cells. Together, higher Cav-1 expression is correlated with worse outcomes, is essential for tumor growth and invasion (both in vitro and in vivo), is responsible for promoting resistance to therapies, and may serve as a prognostic/predictive biomarker and target in PC.

Indexed as

Gene Expression Regulation, NeoplasticRadiation ToleranceSignal TransductionAnimalsCaveolin 1Cell Line, TumorDNA RepairHEK293 CellsHeterograftsHumansMaleMiceMice, NudeNeoplasm MetastasisNeoplasm ProteinsNeoplasm TransplantationCAV1 protein, humanCaveolin 1Neoplasm Proteins

Identifiers

PMID26065715
PMCPMC4464260
OpenAlexW2267744930

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.