Evidence map›Paper›PMID 25961581›Full record

ArticlePloS one2015

Ano1/TMEM16A Overexpression Is Associated with Good Prognosis in PR-Positive or HER2-Negative Breast Cancer Patients following Tamoxifen Treatment.

Huizhe Wu, Shu Guan, Mingli Sun, Zhaojin Yu, Lin Zhao, Miao He, Haishan Zhao, Weifan Yao, Enhua Wang, Feng Jin and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Journal of personalized medicine · 2023
    Article
  7. Article
  8. Role of ANO1 in tumors and tumor immunity.Journal of cancer research and clinical oncology · 2022
    Review
  9. TMEM16A as a potential treatment target for head and neck cancer.Journal of experimental & clinical cancer research : CR · 2022
    Review
  10. Activation of TMEM16A CaJournal of advanced research · 2021
    Article
  11. Simvastatin inhibits oral squamous cell carcinoma by targeting TMEM16A CaJournal of cancer research and clinical oncology · 2021
    Article
  12. Article
  13. The Prognostic Value and Mechanisms of TMEM16A in Human Cancer.Frontiers in molecular biosciences · 2021
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. 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

12 authors at 2 institutions in 1 country.

Huizhe WuDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, P. R. China.
Shu GuanDepartment of Breast Surgery, First Hospital of China Medical University, Shenyang, Liaoning, P. R. China.
Mingli SunDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, P. R. China.
Zhaojin YuDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, P. R. China.
Lin ZhaoDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, P. R. China.
Miao HeDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, P. R. China.
Haishan ZhaoDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, P. R. China.
Weifan YaoDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, P. R. China.
Enhua WangInstitute of Pathology and Pathophysiology, First Hospital and College of Basic Medical Sciences of China Medical University, Shenyang, Liaoning, P. R. China.
Feng JinDepartment of Breast Surgery, First Hospital of China Medical University, Shenyang, Liaoning, P. R. China.
Qinghuan XiaoDepartment of Ion Channel Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, P. R. China.
Minjie WeiDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning, P. R. China.
China Medical University · CNFirst Hospital of China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The calcium-activated chloride channel Ano1 (TMEM16A) is overexpressed in many tumors. Although Ano1 overexpression is found in breast cancer due to 11q13 amplification, it remains unclear whether signaling pathways are involved in Ano1 overexpression during breast cancer tumorigenesis in vivo. Estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2) have been known to contribute to breast cancer progression. It is unclear whether Ano1 is associated with clinical outcomes in breast cancer patients with different ER, PR and HER2 status. In the present study, we investigated the Ano1 expression in 431 patients with invasive ductal breast carcinoma and 46 patients with fibroadenoma, using immunohistochemistry, and analyzed the association between Ano1 expression and clinical characteristics and outcomes of breast cancer patients with different ER, PR, and HER2 status. Ano1 was overexpressed in breast cancer compared with fibroadenoma. Ano1 was significantly more associated with breast cancer with the lower clinical stage (stage I or II), or triple-negative status. Mostly importantly, Ano1 overexpression was associated with good prognosis in patients with the PR-positive or HER2-negative status, and in patients following tamoxifen treatment. Multivariate Cox regression analysis showed that Ano1 overexpression was a prognostic factor for longer overall survival in PR-positive or HER2-negative patients, and a predictive factor for longer overall survival in patients following tamoxifen treatment. Our findings suggest that Ano1 may be a potential marker for good prognosis in PR-positive or HER2-negative patients following tamoxifen treatment. The PR and HER2 status defines a subtype of breast cancer in which Ano1 overexpression is associated with good prognosis following tamoxifen treatment.

Indexed as

AdultAgedAged, 80 and overAnoctamin-1Biomarkers, TumorBreast NeoplasmsChloride ChannelsErb-b2 Receptor Tyrosine KinasesFemaleHumansImmunohistochemistryIn Vitro TechniquesMiddle AgedNeoplasm ProteinsPrognosisReceptors, ProgesteroneANO1 protein, humanAnoctamin-1Biomarkers, TumorChloride ChannelsERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesNeoplasm ProteinsReceptors, ProgesteroneTamoxifen

Identifiers

PMID25961581
PMCPMC4427473
OpenAlexW326116216

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.