Evidence map›Paper›PMID 32027096›Full record

ArticleCancer medicine2020

Genetic association analysis identifies a role for ANO5 in prostate cancer progression.

Chia-Cheng Yu, Lih-Chyang Chen, Chao-Yuan Huang, Victor C Lin, Te-Ling Lu, Cheng-Hsueh Lee, Shu-Pin Huang, Bo-Ying Bao

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-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

13 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. From Plastics to Prognosis:Diagnostics (Basel, Switzerland) · 2026
    Article
  4. Article
  5. Article
  6. ANO10 Function in Health and Disease.Cerebellum (London, England) · 2023
    Review
  7. Article
  8. CaInternational journal of molecular sciences · 2022
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. 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

8 authors at 7 institutions in 1 country.

Chia-Cheng YuDivision of Urology/Transplant Surgery, Department of Surgery, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.
Lih-Chyang ChenDepartment of Medicine, Mackay Medical College, New Taipei City, Taiwan.
Chao-Yuan HuangDepartment of Urology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan.
Victor C LinDepartment of Urology, E-Da Hospital, Kaohsiung, Taiwan.
Te-Ling LuDepartment of Pharmacy, China Medical University, Taichung, Taiwan.
Cheng-Hsueh LeeDepartment of Urology, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Shu-Pin HuangDepartment of Urology, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Bo-Ying BaoDepartment of Pharmacy, China Medical University, Taichung, Taiwan.ORCID 0000-0001-5510-6513
Kaohsiung Medical University · TWAsia University · TWChina Medical University · TWE-Da Hospital · TWMackay Medical University · TWNational Taiwan University Hospital · TWNational Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anoctamins were originally identified as a family of calcium-activated chloride channels, but recently their roles in the development of different types of malignancies were suggested. Here, we evaluated the associations between 211 common single-nucleotide polymorphisms in 10 anoctamin genes with biochemical recurrence (BCR) after radical prostatectomy (RP) for localized prostate cancer. Four SNPs (ANO4 rs585335, ANO5 rs4622263, ANO7 rs62187431, and ANO10 rs118005571) remained significantly associated with BCR after multiple test correction (P < .05 and q = 0.232) and adjustment for known prognostic factors. Expression quantitative trait loci analysis found that ANO5 rs4622263 C and ANO10 rs118005571 C alleles were associated with decreased mRNA expression levels. Moreover, lower expression of ANO5 was correlated with more advanced tumors and poorer outcomes in two independent prostate cancer cohorts. Taken together, ANO5 rs4622263 was associated with BCR, and ANO5 gene expression was correlated with patient prognosis, suggesting a pivotal role for ANO5 in prostate cancer progression.

Indexed as

Polymorphism, Single NucleotideQuantitative Trait LociAgedAnoctaminsBiomarkers, TumorDisease ProgressionFollow-Up StudiesGenetic TestingHumansMaleMiddle AgedPatient SelectionPrognosisProstatectomyProstatic NeoplasmsSurvival RateANO5 protein, humanAnoctaminsBiomarkers, Tumoranoctaminbiomarkerprognosisprogressionprostate cancer

Identifiers

PMID32027096
PMCPMC7131841
OpenAlexW3005184229

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.