Evidence map›Paper›PMID 29440427›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Cancer-secreted hsa-miR-940 induces an osteoblastic phenotype in the bone metastatic microenvironment via targeting ARHGAP1 and FAM134A.

Kyoko Hashimoto, Hiroki Ochi, Satoko Sunamura, Nobuyoshi Kosaka, Yo Mabuchi, Toru Fukuda, Kenta Yao, Hiroaki Kanda, Keisuke Ae, Atsushi Okawa and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 172 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
172citing papers in PubMed, 4 pooled it
11.3field-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

172 citing papers in PubMed, 4 syntheses or guidelines pooled it, 256 citations in OpenAlex.

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112 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

15 authors at 6 institutions in 1 country.

Kyoko HashimotoDepartment of Physiology and Cell Biology, Tokyo Medical and Dental University (TMDU), Graduate School, 113-8510 Tokyo, Japan.
Hiroki OchiDepartment of Physiology and Cell Biology, Tokyo Medical and Dental University (TMDU), Graduate School, 113-8510 Tokyo, Japan.
Satoko SunamuraDepartment of Physiology and Cell Biology, Tokyo Medical and Dental University (TMDU), Graduate School, 113-8510 Tokyo, Japan.
Nobuyoshi KosakaDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, 104-0045 Tokyo, Japan.
Yo MabuchiDepartment of Biochemistry and Biophysics, Tokyo Medical and Dental University (TMDU), Graduate School, 113-8510 Tokyo, Japan.ORCID 0000-0001-8008-3966
Toru FukudaDepartment of Food Science, Tokyo Seiei College, 124-8530 Tokyo, Japan.
Kenta YaoDepartment of Physiology and Cell Biology, Tokyo Medical and Dental University (TMDU), Graduate School, 113-8510 Tokyo, Japan.
Hiroaki KandaDepartment of Pathology, The Cancer Institute of the Japanese Foundation for Cancer Research, 135-8550 Tokyo, Japan.
Keisuke AeDepartment of Orthopaedic Oncology, Cancer Institute Ariake Hospital, 135-8550 Tokyo, Japan.
Atsushi OkawaDepartment of Orthopaedic Surgery, Tokyo Medical and Dental University (TMDU), Graduate School, 113-8510 Tokyo, Japan.
Chihiro AkazawaDepartment of Biochemistry and Biophysics, Tokyo Medical and Dental University (TMDU), Graduate School, 113-8510 Tokyo, Japan.
Takahiro OchiyaDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, 104-0045 Tokyo, Japan.
Mitsuru FutakuchiDepartment of Pathology, Nagasaki University Graduate School of Biomedical Sciences, 852-8523 Nagasaki, Japan.
Shu TakedaDivision of Endocrinology, Toranomon Hospital Endocrine Center, 105-8470 Tokyo, Japan takeda.phy2@tmd.ac.jp satoshin.phy2@tmd.ac.jp.
Shingo SatoDepartment of Physiology and Cell Biology, Tokyo Medical and Dental University (TMDU), Graduate School, 113-8510 Tokyo, Japan; takeda.phy2@tmd.ac.jp satoshin.phy2@tmd.ac.jp.
Tokyo Medical and Dental University · JPJapanese Foundation For Cancer Research · JPNagasaki University · JPThe Cancer Institute Hospital · JPTokyo Seiei College · JPToranomon Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone metastatic lesions are classified as osteoblastic or osteolytic lesions. Prostate and breast cancer patients frequently exhibit osteoblastic-type and osteolytic-type bone metastasis, respectively. In metastatic lesions, tumor cells interact with many different cell types, including osteoblasts, osteoclasts, and mesenchymal stem cells, resulting in an osteoblastic or osteolytic phenotype. However, the mechanisms responsible for the modification of bone remodeling have not been fully elucidated. MicroRNAs (miRNAs) are transferred between cells via exosomes and serve as intercellular communication tools, and numerous studies have demonstrated that cancer-secreted miRNAs are capable of modifying the tumor microenvironment. Thus, cancer-secreted miRNAs can induce an osteoblastic or osteolytic phenotype in the bone metastatic microenvironment. In this study, we performed a comprehensive expression analysis of exosomal miRNAs secreted by several human cancer cell lines and identified eight types of human miRNAs that were highly expressed in exosomes from osteoblastic phenotype-inducing prostate cancer cell lines. One of these miRNAs, hsa-miR-940, significantly promoted the osteogenic differentiation of human mesenchymal stem cells in vitro by targeting

Indexed as

AdenocarcinomaAnimalsBone NeoplasmsBone SubstitutesBreast NeoplasmsCell Line, TumorFemaleGTPase-Activating ProteinsHumansMaleMembrane ProteinsMesenchymal Stem CellsMiceMicroRNAsNeoplasms, ExperimentalProstatic NeoplasmsARHGAP1 protein, humanBone SubstitutesGTPase-Activating ProteinsMembrane ProteinsMicroRNAsMIRN940 microRNA, humanosteobiolRETREG2 protein, humanbone microenvironmentcancer-secreted microRNAexosomeosteoblastic bone metastasisprostate cancer

Identifiers

PMID29440427
PMCPMC5834702
OpenAlexW2794409974

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.