Evidence map›Paper›PMID 28529626›Full record

ArticleTheranostics2017

Cancer-derived Circulating MicroRNAs Promote Tumor Angiogenesis by Entering Dendritic Cells to Degrade Highly Complementary MicroRNAs.

Jiaqi Wang, Huamao Ye, Dandan Zhang, Kai Cheng, Yijun Hu, Xiya Yu, Lei Lu, Jingjing Hu, Changjing Zuo, Baohua Qian and 5 more

Open access · goldAbstract read
In one paragraph

Article in Theranostics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 37 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

15 authors at 3 institutions in 2 countries.

Jiaqi WangChanghai Hospital, Second Military Medical University, Shanghai 200433, China.
Huamao YeChanghai Hospital, Second Military Medical University, Shanghai 200433, China.
Dandan ZhangChanghai Hospital, Second Military Medical University, Shanghai 200433, China.
Kai ChengChanghai Hospital, Second Military Medical University, Shanghai 200433, China.
Yijun HuChanghai Hospital, Second Military Medical University, Shanghai 200433, China.
Xiya YuChanghai Hospital, Second Military Medical University, Shanghai 200433, China.
Lei LuChanghai Hospital, Second Military Medical University, Shanghai 200433, China.
Jingjing HuChanghai Hospital, Second Military Medical University, Shanghai 200433, China.
Changjing ZuoChanghai Hospital, Second Military Medical University, Shanghai 200433, China.
Baohua QianChanghai Hospital, Second Military Medical University, Shanghai 200433, China.
Yongwei YuChanghai Hospital, Second Military Medical University, Shanghai 200433, China.
Shupeng LiuChanghai Hospital, Second Military Medical University, Shanghai 200433, China.
Geng LiuMOE Key Laboratory of Model Animal for Disease Study, Model Animal Research Center of Nanjing University, Nanjing 210061 China.
Chuanbin MaoDepartment of Chemistry and Biochemistry, Stephenson Life Sciences Research Center, University of Oklahoma, 101 Stephenson Parkway, Norman, Oklahoma 73019-5300, USA.
Shanrong LiuChanghai Hospital, Second Military Medical University, Shanghai 200433, China.
Changhai Hospital · CNSecond Military Medical University · CNUniversity of Oklahoma · US

Funding

Virus-based nanoparticles for detecting breast cancer biomarkersR01EB021339 · NIBIB · UNIVERSITY OF OKLAHOMA · PI CAO, BINRUI · 2016 to 2019
$1.4M
Selective tumor inhibition by tumor-homing angiogenesis-suppressing nanofibersR21CA200504 · NCI · UNIVERSITY OF OKLAHOMA · PI MAO, CHUANBIN · 2015 to 2016
$361k
Hiring Non-toxic Virus Nanoparticles to Count Cancer Biomarker MoleculesR21CA195607 · NCI · UNIVERSITY OF OKLAHOMA · PI MAO, CHUANBIN · 2015 to 2016
$359k
NCI NIH HHS R21 CA195607NCI NIH HHS R21 CA200504NIBIB NIH HHS R01 EB021339
6 · The paper itself

Abstract

Understanding the interaction between cancer cells and immunocytes will inspire new cancer therapy strategies. However, how cancer-derived circulating miRNAs modulate such interaction remains unclear. Here we discovered that circulating miR-410-5p, secreted by prostate cancer cells, entered dendritic cells (DCs), with the aid of argonaute-2 protein. The cancer cell antigens stimulated the DCs to produce miR-410-3p, a highly complementary counterpart of miR-410-5p derived from pre-miR-410. The DC-internalized miR-410-5p degraded the miR-410-3p by base pairing and thus inhibited its function in suppressing tumor angiogenesis, promoting tumor growth. Furthermore, blockade of the miR-410-5p upregulated the miR-410-3p to inhibit tumor growth. Our work suggests a new miRNA-mediated role of immunocytes in cancer progression and a new strategy of cancer therapy through suppressing circulating miRNAs.

Indexed as

RNA StabilityAnimalsCell Line, TumorCirculating MicroRNADendritic CellsHumansMaleMice, Inbred C57BLMicroRNAsNeovascularization, PathologicProstatic NeoplasmsCirculating MicroRNAMicroRNAsMIRN410 microRNA, humanMIRN423 microRNA, humanMirn423 microRNA, mousecancer angiogenesiscirculating microRNAdendritic cellsprostate cancer.

Identifiers

PMID28529626
PMCPMC5436502
OpenAlexW2604167833

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.