Evidence map›Paper›PMID 28038461›Full record

ArticleOncotarget2017

Homeobox A11 hypermethylation indicates unfavorable prognosis in breast cancer.

Bingshu Xia, Ming Shan, Ji Wang, Zhenbin Zhong, Jingshu Geng, Xiaohui He, Tung Vu, Dekai Zhang, Da Pang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Review
  7. Oncology reports · 2021
    Article
  8. Article
  9. Methylation inCells · 2020
    Review
  10. The "Janus Face" of Platelets in Cancer.International journal of molecular sciences · 2020
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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 4 institutions in 2 countries.

Bingshu XiaDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150081, China.
Ming ShanDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150081, China.
Ji WangDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150081, China.
Zhenbin ZhongDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150081, China.
Jingshu GengDepartment of Pathology, Harbin Medical University Cancer Hospital, Harbin, 150081, China.
Xiaohui HeDepartment of Medical Records, Harbin Medical University Cancer Hospital, Harbin, 150081, China.
Tung VuCenter for Infectious and Inflammatory Diseases, Institute of Biosciences and Technology, Texas A&M University Health Science Center, Houston, Texas, 77030, USA.
Dekai ZhangCenter for Infectious and Inflammatory Diseases, Institute of Biosciences and Technology, Texas A&M University Health Science Center, Houston, Texas, 77030, USA.
Da PangDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150081, China.
Third Affiliated Hospital of Harbin Medical University · CNHarbin Medical University · CNTexas A&M University · USHeilongjiang Academy of Sciences · CN

Funding

Targeting tumor cell Toll-like receptorR21CA176698 · NCI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ZHANG, DEKAI · 2014 to 2015
$341k
NCI NIH HHS R21 CA176698
6 · The paper itself

Abstract

Homeobox A11 (HOXA11) is one of the hypermethylated genes in breast cancer and its function in breast tumorigenesis remains elusive. In this study, we analyzed the methylation status of HOXA11 in 264 paired breast cancer and normal tissue as well as in matched serum samples by MethyLight assay. Further, the function of HOXA11 in breast tumorigenesis was analyzed by cell proliferation and migration assays. We found that HOXA11 was hypermethylated in cancer tissues (45.08%), especially in invasive ductal carcinomas (P<0.001), patients with a family history of cancer (P=0.033), cases with metastatic lymph nodes (P=0.004) and P53 positive group (P=0.017). Kaplan-Meier survival analysis and Cox regression analysis revealed that HOXA11 hypermethylation is an independent predictor of poor outcomes. The over expression of HOXA11 suppressed cell growth in MDA-MB-231, MCF7, SKBR3 and BT474 cells. In conclusion, the hypermethylation of HOXA11 is an independent prognostic biomarker in breast cancer. Additionally, HOXA11 can be a potential tumor suppressor.

Indexed as

DNA MethylationAdultAgedBiomarkers, TumorBreast NeoplasmsCarcinoma, Ductal, BreastCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseHeredityHomeodomain ProteinsHumansKaplan-Meier EstimateLymphatic MetastasisBiomarkers, TumorHomeodomain ProteinsHOXA11 protein, humanbiomarkerbreast cancerDNA methylationHOX genesprognosis

Identifiers

PMID28038461
PMCPMC5354771
OpenAlexW2566317377

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.