Evidence map›Paper›PMID 28060744›Full record

ReviewOncotarget2017

Targeting macrophage anti-tumor activity to suppress melanoma progression.

Huafeng Wang, Lijuan Zhang, Luhong Yang, Chengfang Liu, Qi Zhang, Linjing Zhang

Open access · diamondAbstract readReview
In one paragraph

Review in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

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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

6 authors at 4 institutions in 1 country.

Huafeng WangModern College of Arts and Science, or School of Life Science, Shanxi Normal University, Linfen, China.
Lijuan ZhangModern College of Arts and Science, or School of Life Science, Shanxi Normal University, Linfen, China.
Luhong YangModern College of Arts and Science, or School of Life Science, Shanxi Normal University, Linfen, China.
Chengfang LiuDepartment of Human Anatomy, Shanxi Medical University, Shanxi Sheng, China.
Qi ZhangNankai Hospital, Tianjin, China.
Linjing ZhangModern College of Arts and Science, or School of Life Science, Shanxi Normal University, Linfen, China.
Shanxi Normal University · CNShanxi Medical University · CNTianjin Medical University · CNTianjin Nankai Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

By phagocytosing cancer cells and their cellular debris, macrophages play a critical role in nonspecific defense (innate immunity) and, as antigen presenters, they help initiate specific defense mechanisms (adaptive immunity). Malignant melanoma is a lethal disease due to its aggressive capacity for metastasis and resistance to therapy. For decades, considerable effort has gone into development of an effective immunotherapy for treatment of metastatic melanoma. In this review, we focus on the anti-tumor activities of macrophages in melanoma and their potential as therapeutic targets in melanoma. Although macrophages can be re-educated through intercellular signaling to promote tumor survival owing to their plasticity, we expect that targeting the anti-tumor activity of macrophages remains a promising strategy for melanoma inhibition. The combination of tumoricidal macrophage activation and other treatments such as surgery, chemotherapy, and radiotherapy, may provide an effective and comprehensive anti-melanoma strategy.

Indexed as

AnimalsDisease ProgressionGranulocyte-Macrophage Colony-Stimulating FactorHumansImmunotherapyMacrophagesMelanomaGranulocyte-Macrophage Colony-Stimulating FactorGM-CSFimmunoadjuvant agentmacrophagemelanoma

Identifiers

PMID28060744
PMCPMC5392344
OpenAlexW2568357586

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.