Evidence map›Paper›PMID 23359505›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Antitumor effect of paclitaxel is mediated by inhibition of myeloid-derived suppressor cells and chronic inflammation in the spontaneous melanoma model.

Alexandra Sevko, Tillmann Michels, Melissa Vrohlings, Ludmila Umansky, Philipp Beckhove, Masashi Kato, Galina V Shurin, Michael R Shurin, Viktor Umansky

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 132 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
132citing papers in PubMed, 2 pooled it
9.4field-weighted citation impact, top 2% 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

132 citing papers in PubMed, 2 syntheses or guidelines pooled it, 240 citations in OpenAlex.

  1. Pooled it
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  5. Systemic Immune Activity Predicts Overall Survival in Treatment-Naïve Patients with Metastatic Pancreatic Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
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  19. Harnessing myeloid cells in cancer.Molecular cancer · 2025
    Review
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72 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

9 authors at 5 institutions in 3 countries.

Alexandra SevkoSkin Cancer Unit, German Cancer Research Center, 69120 Heidelberg, Germany.
Tillmann Michels
Melissa Vrohlings
Ludmila Umansky
Philipp Beckhove
Masashi Kato
Galina V Shurin
Michael R Shurin
Viktor Umansky
German Cancer Research Center · DEHeidelberg University · DEUniversity of Pittsburgh Medical Center · USChubu University · JPUniversity Hospital Heidelberg · DE

Funding

Chemomodulation of the Tumor MicroenvironmentR01CA154369 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SHURIN, MICHAEL R · 2011 to 2015
$1.5M
NCI NIH HHS R01 CA154369
6 · The paper itself

Abstract

The antitumor effects of paclitaxel are generally attributed to the suppression of microtubule dynamics resulting in defects in cell division. New data demonstrated that in ultralow noncytotoxic concentrations, paclitaxel modulated in immune cells in vitro the activity of small Rho GTPases, the key regulators of intracellular actin dynamics. However, the immunomodulatory properties of paclitaxel in vivo have not been evaluated. In this study, using the ret transgenic murine melanoma model, which mimics human cutaneous melanoma, we tested effects of ultralow noncytotoxic dose paclitaxel on functions of myeloid-derived suppressor cells (MDSCs), chronic inflammatory mediators, and T cell activities in the tumor microenvironment in vivo. Administration of paclitaxel significantly decreased accumulation and immunosuppressive activities of tumor-infiltrating MDSCs without alterations of the bone marrow hematopoiesis. This was associated with the inhibition of p38 MAPK activity, TNF-α and production, and S100A9 expression in MDSCs. The production of mediators of chronic inflammation in the tumor milieu also was diminished. Importantly, reduced tumor burden and increased animal survival upon paclitaxel application was mediated by the restoration of CD8 T cell effector functions. We suggest that the ability of paclitaxel in a noncytotoxic dose to block the immunosuppressive potential of MDSCs in vivo represents a new therapeutic strategy to downregulate immunosuppression and chronic inflammation in the tumor microenvironment for enhancing the efficacy of concomitant anticancer therapies.

Indexed as

AnimalsAntineoplastic Agents, PhytogenicCalgranulin BChronic DiseaseDose-Response Relationship, ImmunologicHumansImmunosuppression TherapyInflammationMelanomaMiceMice, Inbred C57BLMice, TransgenicMitogen-Activated Protein KinasesMyeloid CellsPaclitaxelPrimary Cell CultureAntineoplastic Agents, PhytogenicCalgranulin BMitogen-Activated Protein KinasesPaclitaxelS100A9 protein, mouseTumor Necrosis Factor-alpha

Identifiers

PMID23359505
PMCPMC3578135
OpenAlexW1894005600

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.