Evidence map›Paper›PMID 24737320›Full record

ArticleThe Journal of biological chemistry2014

Artemin, a member of the glial cell line-derived neurotrophic factor family of ligands, is HER2-regulated and mediates acquired trastuzumab resistance by promoting cancer stem cell-like behavior in mammary carcinoma cells.

Keshuo Ding, Arindam Banerjee, Sheng Tan, JunSong Zhao, Qian Zhuang, Rui Li, Pengxu Qian, Suling Liu, Zheng-Sheng Wu, Peter E Lobie and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-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

23 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
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  4. JHDM1D-AS1-driven inhibition of miR-940 releases ARTN expression to induce breast carcinogenesis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Article
  5. Review
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  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
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  13. Article
  14. Review
  15. Article
  16. Article
  17. Artemin promotes proliferation and metastasis in human laryngeal squamous cell carcinoma.International journal of clinical and experimental pathology · 2017
    Article
  18. Neurotrophic Factors and Their Potential Applications in Tissue Regeneration.Archivum immunologiae et therapiae experimentalis · 2016
    Review
  19. Article
  20. Review
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

11 authors at 4 institutions in 2 countries.

Keshuo DingFrom the Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei, Anhui 230027, People's Republic of China.
Arindam Banerjeethe Cancer Science Institute of Singapore and Department of Pharmacology, National University of Singapore, Singapore 117599, and.
Sheng TanFrom the Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei, Anhui 230027, People's Republic of China.
JunSong ZhaoFrom the Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei, Anhui 230027, People's Republic of China.
Qian ZhuangFrom the Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei, Anhui 230027, People's Republic of China.
Rui LiFrom the Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei, Anhui 230027, People's Republic of China.
Pengxu QianFrom the Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei, Anhui 230027, People's Republic of China.
Suling LiuFrom the Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei, Anhui 230027, People's Republic of China.
Zheng-Sheng WuFrom the Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei, Anhui 230027, People's Republic of China, the Department of Pathology, Anhui Medical University, Hefei, Anhui 230032, People's Republic of China, the Department of Pathology, Shanghai Medical College, Fudan University, Yangpu, Shanghai, China.
Peter E Lobiethe Cancer Science Institute of Singapore and Department of Pharmacology, National University of Singapore, Singapore 117599, and the National Cancer Institute of Singapore, National University Health System, Singapore 119074 csipel@nus.edu.sg.
Tao ZhuFrom the Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei, Anhui 230027, People's Republic of China, zhut@ustc.edu.cn.
University of Science and Technology of China · CNNational University Cancer Institute, Singapore · SGNational University of Singapore · SGShanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous studies have demonstrated that Artemin (ARTN) functions as a cancer stem cell (CSC) and metastatic factor in mammary carcinoma. Herein, we report that ARTN mediates acquired resistance to trastuzumab in HER2-positive mammary carcinoma cells. Ligands that increase HER2 activity increased ARTN expression in HER2-positive mammary carcinoma cells, whereas trastuzumab inhibited ARTN expression. Forced expression of ARTN decreased the sensitivity of HER2-positive mammary carcinoma cells to trastuzumab both in vitro and in vivo. Conversely, siRNA-mediated depletion of ARTN enhanced trastuzumab efficacy. Cells with acquired resistance to trastuzumab exhibited increased ARTN expression, the depletion of which restored trastuzumab sensitivity. Trastuzumab resistance produced an increased CSC population concomitant with enhanced mammospheric growth. ARTN mediated the enhancement of the CSC population by increased BCL-2 expression, and the CSC population in trastuzumab-resistant cells was abrogated upon inhibition of BCL-2. Hence, we conclude that ARTN is one mediator of acquired resistance to trastuzumab in HER2-positive mammary carcinoma cells.

Indexed as

Antibodies, Monoclonal, HumanizedBase SequenceBreast NeoplasmsCell Line, TumorDNA PrimersDrug Resistance, NeoplasmErb-b2 Receptor Tyrosine KinasesFemaleGlial Cell Line-Derived Neurotrophic FactorHumansNeoplastic Stem CellsNerve Tissue ProteinsPolymerase Chain ReactionTrastuzumabAntibodies, Monoclonal, HumanizedARTN protein, humanDNA PrimersERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesGlial Cell Line-Derived Neurotrophic FactorNerve Tissue ProteinsTrastuzumabBreast CancerCancer Stem CellsChemoresistanceOncogeneTumor Metastases

Identifiers

PMID24737320
PMCPMC4047380
OpenAlexW2036902611

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.