Evidence map›Paper›PMID 27613132›Full record

ReviewAdvances in cancer research2016

Immune Regulation of the Metastatic Process: Implications for Therapy.

A de Mingo Pulido, B Ruffell

Abstract readReview
In one paragraph

Review in Advances in cancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
14.4field-weighted citation impact, top 1% 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

6 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. The Immune Microenvironment and Cancer Metastasis.Cold Spring Harbor perspectives in medicine · 2020
    Review
  4. Article
  5. Article
  6. Review
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

2 authors at 1 institution in 1 country.

A de Mingo PulidoH. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, United States.
B RuffellH. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, United States. Electronic address: brian.ruffell@moffitt.org.
Moffitt Cancer Center · US

Funding

Regulating Intratumoral Leukocytes to Improve Response to ChemotherapyR00CA185325 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI RUFFELL, BRIAN · 2015 to 2017
$752k
NCI NIH HHS R00 CA185325
6 · The paper itself

Abstract

Metastatic disease is the major cause of fatalities in cancer patients, but few therapies are designed to target the metastatic process. Cancer cells must perform a number of steps to successfully establish metastatic foci, including local invasion, intravasation, survival, extravasation, and growth in ectopic tissue. Due to the nonrandom distribution of metastasis, it has long been recognized that the tissue microenvironment must be an important determinant of colonization. More recently it has been established in animal models that immune cells regulate the metastatic process, including a dominant role for monocytes and macrophages, and emerging roles for neutrophils and various lymphocyte populations. While most research has focused on the early dissemination process, patients usually present clinically with disseminated, if not macroscopic, disease. Identifying pathways by which immune cells regulate growth and therapeutic resistance within metastatic sites is therefore key to the development of pharmacological agents that will significantly extend patient survival.

Indexed as

ImmunotherapyAnimalsAntineoplastic AgentsHumansNeoplasm MetastasisNeoplasmsTumor MicroenvironmentAntineoplastic AgentsChemotherapyImmuneImmunotherapyLeukocyteLymphocyteMacrophageMetastasisMonocyteNeutrophilsTumor

Identifiers

PMID27613132
PMCPMC5364524
OpenAlexW2432307783

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.