Evidence map›Paper›PMID 26716419›Full record

ArticleOncotarget2016

FZD7 regulates BMSCs-mediated protection of CML cells.

Na Liu, Shaolei Zang, Yan Liu, Yingqiao Wang, Wei Li, Qiang Liu, Min Ji, Daoxin Ma, Chunyan Ji

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Oncology letters · 2020
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Frizzled-7 is required forBiology open · 2017
    Article
  10. Article
  11. 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 2 institutions in 1 country.

Na LiuDepartment of Hematology Qilu Hospital, Shandong University, Ji'nan 250012, China.
Shaolei ZangDepartment of Hematology Qilu Hospital, Shandong University, Ji'nan 250012, China.
Yan LiuDepartment of Hematology Qilu Hospital, Shandong University, Ji'nan 250012, China.
Yingqiao WangDepartment of Hematology Qilu Hospital, Shandong University, Ji'nan 250012, China.
Wei LiDepartment of Hematology Qilu Hospital, Shandong University, Ji'nan 250012, China.
Qiang LiuMedical Research Center, Shandong Provincial Qianfoshan Hospital, Shandong University, Ji'nan 250014, China.
Min JiDepartment of Hematology Qilu Hospital, Shandong University, Ji'nan 250012, China.
Daoxin MaDepartment of Hematology Qilu Hospital, Shandong University, Ji'nan 250012, China.
Chunyan JiDepartment of Hematology Qilu Hospital, Shandong University, Ji'nan 250012, China.
Qilu Hospital of Shandong University · CNShandong Provincial QianFoShan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inspite of effective treatment with imatinib (IM), chronic myeloid leukemia (CML) is still an incurable disease. Some patients became refractory because of IM resistance. Bone marrow mesenchymal stem cells (BMSCs) have been implicated a role in promoting CML cells' resistance against IM treatment. The detailed molecular mechanisms, however, remain largely unknown. In this study, we found that BMSCs increased the expression of FZD7 and activated Wnt/β-catenin signaling pathway in CML cells. BMSCs from CML patients showed increased efficiency to accelerate CML cell proliferation, enhance the drug resistance of K562 cells and up-regulate the expression of FZD7. Antagonism of FZD7 expression by shRNA significantly suppressed proliferation and increased IM sensitivity of CML cells co-cultured with BMSCs cells. Our findings suggest that FZD7, involved in canonical Wnt signaling pathway, plays a critical role in mediating BMSCs-dependent protection of CML cells, and potentially provide a novel therapeutic target for CML.

Indexed as

Antineoplastic AgentsApoptosisBone Marrow CellsCase-Control StudiesCell ProliferationDown-RegulationFrizzled ReceptorsHumansImatinib MesylateK562 CellsLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMesenchymal Stem CellsRNA, Small InterferingTransfectionWnt Signaling PathwayAntineoplastic AgentsFrizzled ReceptorsFZD7 protein, humanImatinib MesylateRNA, Small InterferingBMSCsCMLFZD7imatinib sensitivityWnt signaling pathway

Identifiers

PMID26716419
PMCPMC4868748
OpenAlexW2221059153

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.