Evidence map›Paper›PMID 30536376›Full record

ArticleJournal of cellular physiology2019

Artemisinin inhibits breast cancer-induced osteolysis by inhibiting osteoclast formation and breast cancer cell proliferation.

Jia Li, Wenyu Feng, Huiping Lu, Yan Wei, Shiting Ma, Linfeng Wei, Qian Liu, Jinmin Zhao, Qingjun Wei, Jun Yao

Erratum issuedAbstract read
In one paragraph

Article in Journal of cellular physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

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  12. The role of macrophages during breast cancer development and response to chemotherapy.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Jia LiDepartment of Pathology, The First Affliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Wenyu FengDepartment of Orthopaedic Surgery, The First Affliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.ORCID 0000-0003-0937-9670
Huiping LuDepartment of Pathology, The First Affliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Yan WeiDepartment of Pathology, The First Affliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Shiting MaDepartment of Orthopaedic Surgery, The First Affliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Linfeng WeiDepartment of Orthopaedic Surgery, The First Affliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Qian LiuResearch Centre for Regenerative Medicine and Guangxi Key Laboratory of Regenerative Medicine, Guangxi Medical University, Nanning, People's Republic of China.
Jinmin ZhaoDepartment of Orthopaedic Surgery, The First Affliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Qingjun WeiDepartment of Orthopaedic Surgery, The First Affliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Jun YaoResearch Centre for Regenerative Medicine and Guangxi Key Laboratory of Regenerative Medicine, Guangxi Medical University, Nanning, People's Republic of China.
Guangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In addition to being used to treat malaria, artemisinin (Art) can be used as an anti-inflammatory and antitumor agent. In this study, we evaluated the effects of Art on osteoclast formation and activation and on the development of breast cancer cells in bone. To evaluate the effect of Art on osteoclast differentiation in vitro, we treated bone marrow-derived macrophages (BMMs) with various concentrations of Art and evaluated the expression of genes and proteins involved in osteoclast formation. We also performed cell counting kit-8 assays to evaluate the toxicity of Art in BMMs and MDA-MB-231 cells. We also performed Transwell assays, wound-healing assays, colony formation assays, and cell apoptosis assays to evaluate the effect of Art in MDA-MB-231 cells. We also evaluated the effect of Art in an in vivo osteoclast bone resorption assay using a nude mouse model. We demonstrated that Art inhibits the differentiation and establishment of osteoclasts even though Art is not toxic to osteoclasts. In addition, Art reduced expression of genes involved in osteoclast formation and inhibited osteoclast bone resorption in a concentration-dependent manner. Based on our data, we believe that Art can inhibit proliferation of breast cancer cells by activating apoptosis pathways, and inhibit osteoclast formation and differentiation by inhibiting activation of cathepsin K, ATPase H+ transporting V0 subunit D2, nuclear factor of activated T cells 1, calcitonin receptor, and tartrate-resistant acid phosphatase and by inhibiting nuclear factor-κB activation.

Indexed as

AnimalsApoptosisArtemisininsBone Marrow CellsBreast NeoplasmsCathepsin KCell DifferentiationCell Line, TumorCell ProliferationMiceMice, Inbred C57BLMice, NudeNFATC Transcription FactorsNF-kappa BOsteoclastsOsteolysisArtemisininsCathepsin KNFATC Transcription FactorsNF-kappa BProton-Translocating ATPasesReceptors, CalcitoninTartrate-Resistant Acid Phosphataseartemisininbreast cancerosteoclastRANKL

Identifiers

PMID30536376
PMCPMC13484186
OpenAlexW2905472567

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.