Evidence map›Paper›PMID 25193509›Full record

ArticleMolecular cancer therapeutics2014

Bisphosphonates inhibit stellate cell activity and enhance antitumor effects of nanoparticle albumin-bound paclitaxel in pancreatic ductal adenocarcinoma.

Vianey Gonzalez-Villasana, Cristian Rodriguez-Aguayo, Thiruvengadam Arumugam, Zobeida Cruz-Monserrate, Enrique Fuentes-Mattei, Defeng Deng, Rosa F Hwang, Huamin Wang, Cristina Ivan, Raul Joshua Garza and 14 more

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  4. Review
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  13. Rac1/Pak1/p38/MMP-2 Axis Regulates Angiogenesis in Ovarian Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    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

24 authors at 1 institution in 1 country.

Vianey Gonzalez-VillasanaDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cristian Rodriguez-AguayoDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Thiruvengadam ArumugamDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Zobeida Cruz-MonserrateDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Enrique Fuentes-MatteiDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Defeng DengDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Rosa F HwangDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Huamin WangDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cristina IvanDepartment of Gynecologic Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Raul Joshua GarzaDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Evan CohenDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Hui GaoDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Guillermo N Armaiz-PenaDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas. Department of Gynecologic Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Paloma Del C Monroig-BosqueDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas. University of Puerto Rico School of Medicine, San Juan, Puerto Rico.
Bincy PhilipDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Mohammed H RashedDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas. Al-Azhar University, Cairo, Egypt.
Burcu AslanDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Mumin Alper ErdoganDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Yolanda Gutierrez-PuenteUniversidad Autonoma de Nuevo Leon, San Nicolas de los Garza, Nuevo Leon, Mexico.
Bulent OzpolatDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
James M ReubenDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Anil K SoodDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas. Department of Gynecologic Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas. Center for RNAi and Non-coding RNA, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Craig LogsdonDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Gabriel Lopez-BeresteinDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas. Center for RNAi and Non-coding RNA, The University of Texas MD Anderson Cancer Center, Houston, Texas. glopez@mdanderson.org.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
UNIVERSITY OF TEXAS MD ANDERSON SPORE IN OVARIAN CANCERP50CA083639 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BAST, ROBERT C · 1999 to 2015
$33.0M
UPR/MDACC Partnership for Excellence in Cancer Research (Luis Segarra supplement)U54CA096300 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Lauren Elizabeth Colbert · 2002 to 2026
$23.8M
Texas Center for Cancer NanomedicineU54CA151668 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FERRARI, MAURO · 2010 to 2014
$12.4M
TRANS-NETWORK PROJECTSU54CA143837 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FERRARI, MAURO · 2009 to 2014
$10.8M
Subcellular localization of nanoparticlesRC2GM092599 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CHIU, WAH, DECUZZI, PAOLO · 2009 to 2010
$3.0M
Novel extra cellular RNA-based combinatorial RNA inhibition therapyUH2TR000943 · NCATS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CALIN, GEORGE A., LOPEZ-BERESTEIN, GABRIEL · 2013 to 2014
$1.1M
(PQD3) The role and therapeutic potential of ZNF304 in Ovarian CancerR21CA180145 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LOPEZ-BERESTEIN, GABRIEL, OZPOLAT, BULENT · 2013 to 2014
$378k
NCATS NIH HHS NCI-UH2TR00943NCATS NIH HHS UH2 TR000943NCI NIH HHS CA151668NCI NIH HHS CA180145NCI NIH HHS NCI-CA151668NCI NIH HHS NCI-U54CA096300NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA083639NCI NIH HHS R21 CA180145NCI NIH HHS U54 CA096300NCI NIH HHS U54 CA143837NCI NIH HHS U54CA143837NCI NIH HHS U54 CA151668NCI NIH HHS U54CA151668NIGMS NIH HHS RC2 GM092599NIGMS NIH HHS RC2GM092599PHS HHS NCI-P50PKCA093459
6 · The paper itself

Abstract

Pancreatic stellate cells (PSC) have been recognized as the principal cells responsible for the production of fibrosis in pancreatic ductal adenocarcinoma (PDAC). Recently, PSCs have been noted to share characteristics with cells of monocyte-macrophage lineage (MML cells). Thus, we tested whether PSCs could be targeted with the nitrogen-containing bisphosphonates (NBP; pamidronate or zoledronic acid), which are potent MML cell inhibitors. In addition, we tested NBPs treatment combination with nanoparticle albumin-bound paclitaxel (nab-paclitaxel) to enhance antitumor activity. In vitro, we observed that PSCs possess α-naphthyl butyrate esterase (ANBE) enzyme activity, a specific marker of MML cells. Moreover, NBPs inhibited PSCs proliferation, activation, release of macrophage chemoattractant protein-1 (MCP-1), and type I collagen expression. NBPs also induced PSCs apoptosis and cell-cycle arrest in the G1 phase. In vivo, NBPs inactivated PSCs; reduced fibrosis; inhibited tumor volume, tumor weight, peritoneal dissemination, angiogenesis, and cell proliferation; and increased apoptosis in an orthotopic murine model of PDAC. These in vivo antitumor effects were enhanced when NBPs were combined with nab-paclitaxel but not gemcitabine. Our study suggests that targeting PSCs and tumor cells with NBPs in combination with nab-paclitaxel may be a novel therapeutic approach to PDAC.

Indexed as

AdultAlbuminsAnimalsApoptosisCarcinoma, Pancreatic DuctalCell Line, TumorCell ProliferationDiphosphonatesDrug SynergismFemaleHumansImmunohistochemistryMiceMice, NudeNanoparticlesPaclitaxelAlbuminsDiphosphonatesPaclitaxelPamidronate

Identifiers

PMID25193509
PMCPMC4221441
OpenAlexW1973665853

What OpenQuestion holds

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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.