Evidence map›Paper›PMID 27157622›Full record

ArticleOncogene2016

miR-135b, a key regulator of malignancy, is linked to poor prognosis in human myxoid liposarcoma.

Y Nezu, K Hagiwara, Y Yamamoto, T Fujiwara, K Matsuo, A Yoshida, A Kawai, T Saito, T Ochiya

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

33 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Liposarcoma: State of the Art-A Scoping Review.Medical sciences (Basel, Switzerland) · 2026
    Article
  3. Review
  4. Article
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  16. Article
  17. Article
  18. Molecular signatures of tumor progression in myxoid liposarcoma identified by N-glycan mass spectrometry imaging.Laboratory investigation; a journal of technical methods and pathology · 2020
    Article
  19. Article
  20. 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

9 authors at 3 institutions in 1 country.

Y NezuDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.
K HagiwaraDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.
Y YamamotoDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.
T FujiwaraDepartment of Orthopaedic Surgery, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama, Japan.
K MatsuoDepartment of Orthopaedic Surgery, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
A YoshidaDivision of Pathology and Clinical Laboratories, National Cancer Center Hospital, Tokyo, Japan.
A KawaiDivision of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
T SaitoDepartment of Orthopaedic Surgery, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
T OchiyaDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.
Yokohama City University · JPOkayama University · JPTokyo National Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myxoid/round cell (RC) liposarcomas (MLS) were originally classified into two distinct populations based on histological differences; a myxoid component and a RC component. It is notable that, depending on an increase of the RC component, the prognosis significantly differs. Hence, the RC component is associated with metastasis and poor prognosis. However, the molecular mechanisms that contribute to the malignancy of the RC component still remain largely unknown. Here, we report microRNA-135b (miR-135b), a key regulator of the malignancy, highly expressed in the RC component and promoting MLS cell invasion in vitro and metastasis in vivo through the direct suppression of thrombospondin 2 (THBS2). Decreased THBS2 expression by miR-135b increases the total amount of matrix metalloproteinase 2 (MMP2) and influences cellular density and an extracellular matrix structure, thereby resulting in morphological change in tumor. The expression levels of miR-135b and THBS2 significantly correlated with a poor prognosis in MLS patients. Overall, our study reveals that the miR-135b/THBS2/MMP2 axis is tightly related to MLS pathophysiology and has an important clinical implication. This work provides noteworthy evidence for overcoming metastasis and improving patient outcomes, and sheds light on miR-135b and THBS2 as novel molecular targets for diagnosis and therapy in MLS.

Indexed as

Gene Expression Regulation, Neoplastic3' Untranslated RegionsAnimalsCell Line, TumorCell MovementDisease Models, AnimalGene Expression ProfilingGene SilencingHigh-Throughput Nucleotide SequencingHumansLiposarcoma, MyxoidLung NeoplasmsMatrix Metalloproteinase 2MiceMice, KnockoutMicroRNAs3' Untranslated RegionsMatrix Metalloproteinase 2MicroRNAsMIRN135 microRNA, humanThrombospondin 2Thrombospondins

Identifiers

PMID27157622
PMCPMC5143367
OpenAlexW2346457782

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.