Evidence map›Paper›PMID 27340348›Full record

ReviewWorld journal of gastroenterology2016

MicroRNAs: Novel immunotherapeutic targets in colorectal carcinoma.

Xiang Li, Jing Nie, Qian Mei, Wei-Dong Han

Open access · hybridAbstract readReview
In one paragraph

Review in World journal of gastroenterology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 8% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

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  20. Relationship betweenWorld journal of gastroenterology · 2018
    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

4 authors at 2 institutions in 2 countries.

Xiang LiXiang Li, Jing Nie, Qian Mei, Wei-Dong Han, Department of Molecular Biology, School of Life Sciences, Chinese PLA General Hospital, Beijing 100853, China.
Jing NieXiang Li, Jing Nie, Qian Mei, Wei-Dong Han, Department of Molecular Biology, School of Life Sciences, Chinese PLA General Hospital, Beijing 100853, China.
Qian MeiXiang Li, Jing Nie, Qian Mei, Wei-Dong Han, Department of Molecular Biology, School of Life Sciences, Chinese PLA General Hospital, Beijing 100853, China.
Wei-Dong HanXiang Li, Jing Nie, Qian Mei, Wei-Dong Han, Department of Molecular Biology, School of Life Sciences, Chinese PLA General Hospital, Beijing 100853, China.
Chinese PLA General Hospital · CNCreative Research Enterprises (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal carcinoma (CRC) is one of the most common types of cancer worldwide and the prognosis for CRC patients with recurrence or metastasis is extremely poor. Although chemotherapy and radiation therapy can improve survival, there are still numerous efforts to be performed. Immunotherapy is frequently used, either alone or in combination with other therapies, for the treatment of CRC and is a safe and feasible way to improve CRC treatment. Furthermore, the significance of the immune system in the biology of CRC has been demonstrated by retrospective assessments of immune infiltrates in resected CRC tumors. MicroRNAs (miRNAs) are short, non-coding RNAs that can regulate multiple target genes at the post-transcriptional level and play critical roles in cell proliferation, differentiation and apoptosis. MiRNAs are required for normal immune system development and function. Nevertheless, aberrant expression of miRNAs is often observed in various tumor types and leads to immune disorders or immune evasion. The immunomodulatory function of miRNAs indicates that miRNAs may ultimately be part of the portfolio of anti-cancer targets. Herein, we will review the potential roles of miRNAs in the regulation of the immune response in CRC and then move on to discuss how to utilize different miRNA targets to treat CRC. We also provide an overview of the major limitations and challenges of using miRNAs as immunotherapeutic targets.

Indexed as

ApoptosisBiomarkers, TumorCarcinogenesisCell DifferentiationCell ProliferationColorectal NeoplasmsGene Expression Regulation, NeoplasticHumansImmunity, CellularImmunotherapyMicroRNAsMolecular Targeted TherapyNeoplasm Recurrence, LocalPrognosisSignal TransductionTumor MicroenvironmentBiomarkers, TumorMicroRNAsColorectal carcinomaImmune responseImmunotherapyInflammationInflammatory bowel diseasemicroRNAsTumor microenvironment

Identifiers

PMID27340348
PMCPMC4910653
OpenAlexW2413100463

What OpenQuestion holds

Textmetadata
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.