Evidence map›Paper›PMID 31288064›Full record

ArticleCancer letters2019

Improved anti-tumor efficacy of paclitaxel in combination with MicroRNA-125b-based tumor-associated macrophage repolarization in epithelial ovarian cancer.

Neha N Parayath, Srujan Kumar Gandham, Fraser Leslie, Mansoor M Amiji

Open access · greenAbstract read
In one paragraph

Article in Cancer letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 citations in OpenAlex.

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  17. Current Update on Nanotechnology-Based Approaches in Ovarian Cancer Therapy.Reproductive sciences (Thousand Oaks, Calif.) · 2023
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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

4 authors at 2 institutions in 1 country.

Neha N ParayathDepartment of Pharmaceutical Sciences, School of Pharmacy, Boston, MA, 02115, USA.
Srujan Kumar GandhamDepartment of Pharmaceutical Sciences, School of Pharmacy, Boston, MA, 02115, USA.
Fraser LeslieDepartment of Pharmaceutical Sciences, School of Pharmacy, Boston, MA, 02115, USA.
Mansoor M AmijiDepartment of Pharmaceutical Sciences, School of Pharmacy, Boston, MA, 02115, USA; Department of Chemical Engineering, College of Engineering, Northeastern University, Boston, MA, 02115, USA. Electronic address: m.amiji@northeastern.edu.
Massachusetts College of Pharmacy and Health Sciences · USNortheastern University · US

Funding

Reprogramming Tumor-Associated Macrophages in PDAC with MicroRNA Nano-VectorsR21CA213114 · NCI · NORTHEASTERN UNIVERSITY · PI AMIJI, MANSOOR M., MACKENZIE, GERARDO GUILLERMO · 2017 to 2018
$388k
Targeted Platinates/siRNA Combination Therapy for Resistant Lung CancerR21CA179652 · NCI · NORTHEASTERN UNIVERSITY · PI AMIJI, MANSOOR M., IYER, ARUN · 2014 to 2015
$372k
Integrated Nano-Therapeutics to Overcome Tumor Plasticity and ResistanceR56CA198492 · NCI · NORTHEASTERN UNIVERSITY · PI AMIJI, MANSOOR M. · 2017 to 2017
$300k
NCI NIH HHS R21 CA179652NCI NIH HHS R21 CA213114NCI NIH HHS R56 CA198492
6 · The paper itself

Abstract

In epithelial ovarian cancers, the presence of tumor-associated macrophages (TAMs) is well correlated with the poor disease outcomes. TAMs are know to suppress the immune system, induce pro-tumoral functions and inhibit anti-tumor responses associated with chemotherapy. In this study, we have evaluated the synergistic efficacy of TAM repolarization and intraperitoneal paclitaxel in epithelial ovarian cancers. We demonstrate that hyaluronic acid-based nanoparticles encapsulating miR-125b (HA-PEI-miR-125b) can specifically target TAMs in the peritoneal cavity of a syngeneic ID8-VEGF ovarian cancer mouse model and can repolarize macrophages to an immune-activating phenotype. These HA-PEI-miR-125b nanoparticles in combination with intraperitoneal paclitaxel can enhance the anti-tumor efficacy of paclitaxel during the later stages of disease progression as seen by the significant reduction in the ascitic fluid and peritoneal VEGF levels. Furthermore, these HA-PEI-miR-125b nanoparticles do not induce systemic toxicity and thus warrant a further evaluation in the clinical setting.

Indexed as

AnimalsAntineoplastic Agents, PhytogenicApoptosisBiomarkers, TumorCarcinoma, Ovarian EpithelialCell ProliferationCombined Modality TherapyDrug Delivery SystemsFemaleGene Expression Regulation, NeoplasticHumansHyaluronic AcidMacrophages, PeritonealMiceMice, Inbred C57BLMice, NudeAntineoplastic Agents, PhytogenicBiomarkers, TumorHyaluronic AcidMicroRNAsMIRN125 microRNA, humanPaclitaxelChemotherapyHyaluronic acid-poly(ethylene imine) nanoparticlesID8-VEGF ovarian cancer modelImmune-suppressive macrophagesIntraperitoneal chemotherapy

Identifiers

PMID31288064
PMCPMC6682447
OpenAlexW2955316852

What OpenQuestion holds

Textmetadata
LicenceTDM
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.