Evidence map›Paper›PMID 34094689›Full record

ArticleAmerican journal of cancer research2021

Association between the polygenic liabilities for prostate cancer and breast cancer with biochemical recurrence after radical prostatectomy for localized prostate cancer.

Shi-Heng Wang, Shu-Pin Huang, Yi-Jiun Pan, Po-Chang Hsiao, Chia-Yang Li, Lih-Chyang Chen, Chia-Cheng Yu, Chao-Yuan Huang, Victor C Lin, Te-Ling Lu and 1 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

11 authors at 5 institutions in 1 country.

Shi-Heng WangDepartment of Occupational Safety and Health, China Medical University Taichung 404, Taiwan.
Shu-Pin HuangDepartment of Urology, Kaohsiung Medical University Hospital Kaohsiung 807, Taiwan.
Yi-Jiun PanSchool of Medicine, China Medical University Taichung 404, Taiwan.
Po-Chang HsiaoInstitute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University Taipei 100, Taiwan.
Chia-Yang LiGraduate Institute of Medicine, College of Medicine, Kaohsiung Medical University Kaohsiung 807, Taiwan.
Lih-Chyang ChenDepartment of Medicine, Mackay Medical College New Taipei 252, Taiwan.
Chia-Cheng YuDivision of Urology, Department of Surgery, Kaohsiung Veterans General Hospital Kaohsiung 813, Taiwan.
Chao-Yuan HuangDepartment of Urology, National Taiwan University Hospital, College of Medicine, National Taiwan University Taipei 100, Taiwan.
Victor C LinDepartment of Urology, E-Da Hospital Kaohsiung 824, Taiwan.
Te-Ling LuDepartment of Pharmacy, China Medical University Taichung 404, Taiwan.
Bo-Ying BaoDepartment of Pharmacy, China Medical University Taichung 404, Taiwan.
China Medical University · TWKaohsiung Medical University · TWMackay Medical College · TWNational Taiwan University · TWNational Taiwan University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate and breast cancers are hormone-related malignancies and are characterized by a complex interplay of hundreds of susceptibility loci throughout the genome. Prostate cancer could be inhibited by eliminating androgens through castration or estrogen administration, thus facilitating long-term treatment of prostate cancer; however, the role of estrogen in prostate cancer remains unclear. This study aimed to determine whether polygenic risk scores (PRSs) comprising combinations of genome-wide susceptibility variants influence the clinical outcomes of prostate cancer patients. The study subjects were recruited from four medical centers in Taiwan, and genome-wide genotyping data were obtained from 643 prostate cancer patients. We derived the PRS for prostate cancer (PRS-PC) and for breast cancer (PRS-BC) for each patient. The association between the PRS-PC/PRS-BC at the age of prostate cancer onset and recurrence within seven years was evaluated using a regression model adjusted for population stratification components. A higher PRS-PC was associated with an earlier onset age for prostate cancer (beta in per SD increase in PRS = -0.89,

Indexed as

biochemical recurrencebreast cancerPolygenic risk scoreprostate cancerradical prostatectomy

Identifiers

PMID34094689
PMCPMC8167673
OpenAlexW3170301542

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.