Evidence map›Paper›PMID 27147578›Full record

ArticleOncotarget2016

Potential options for managing LOX+ ER- breast cancer patients.

Yong Han, Shenyi Lian, Xingran Cui, Kexin Meng, Balázs Győrffy, Tao Jin, Dongsheng Huang

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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. ATP7A delivers copper to the lysyl oxidase family of enzymes and promotes tumorigenesis and metastasis.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  4. Article
  5. 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

7 authors at 4 institutions in 3 countries.

Yong HanClinical Research Institute, Zhejiang Provincial People's Hospital, Hangzhou, China.
Shenyi LianKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Biochemistry and Molecular Biology, Peking University Cancer Hospital and Institute, Beijing, China.
Xingran CuiDivision of Interdisciplinary Medicine and Biotechnology, Department of Medicine, Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, Massachusetts, USA.
Kexin MengDepartment of Thyroid Breast Surgery, Zhejiang Provincial People's Hospital, Hangzhou, China.
Balázs GyőrffyMomentum Cancer Biomarker Research Group, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary.
Tao JinDepartment of Cardiothoracic Surgery, Zhejiang Provincial People's Hospital, Hangzhou, China.
Dongsheng HuangClinical Research Institute, Zhejiang Provincial People's Hospital, Hangzhou, China.
Zhejiang Provincial People's Hospital · CNBeth Israel Deaconess Medical Center · USPeking University · CNSemmelweis University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overexpression of lysyl oxidase (LOX) is often observed in estrogen receptor negative (ER-) breast cancer patients with bone metastasis. In the present bioinformatics study, we observed that LOX is a prognostic factor for poor progression free survival in patients with ER- breast cancer. LOX overexpression was positively correlated with resistance to radiation, doxorubin and mitoxantrone, but negatively correlated with resistance to bisphosphonate, PARP1 inhibitors, cisplatin, trabectedin and gemcitabine. LOX overexpression was also associated with EMT and stemness of cancer cells, which leads to chemotherapeutic resistance and poor outcome in ER- patients. Although we suggest several therapeutic interventions that may help in the management of LOX+ ER- breast cancer patients, experiments to validate the function of LOX in ER- breast cancer are still needed.

Indexed as

Antineoplastic AgentsBiomarkers, TumorBreast NeoplasmsComputational BiologyDatabases, GeneticDiphosphonatesDisease-Free SurvivalDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionEstrogen Receptor alphaFemaleHumansProtein-Lysine 6-OxidaseRadiation ToleranceTime FactorsTreatment OutcomeAntineoplastic AgentsBiomarkers, TumorDiphosphonatesESR1 protein, humanEstrogen Receptor alphaProtein-Lysine 6-OxidasebisphosphonateschemoresistanceEMTestrogen recepterLOX

Identifiers

PMID27147578
PMCPMC5078060
OpenAlexW2344367141

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.