Evidence map›Paper›PMID 27227944›Full record

Observational studyMedicine2016

PD-1 rs2227982 Polymorphism Is Associated With the Decreased Risk of Breast Cancer in Northwest Chinese Women: A Hospital-Based Observational Study.

Hong-Tao Ren, Yi-Ming Li, Xi-Jing Wang, Hua-Feng Kang, Tian-Bo Jin, Xiao-Bin Ma, Xing-Han Liu, Meng Wang, Kang Liu, Peng Xu and 2 more

Abstract readObservational Study
In one paragraph

Observational study in Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

34 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Genotype and Haplotype Analysis BetweenHealth science reports · 2025
    Article
  6. Article
  7. Article
  8. Impact of MIR31HG polymorphisms on risk of breast cancer in Chinese women.International journal of clinical oncology · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Association ofPharmacogenomics and personalized medicine · 2022
    Article
  14. Article
  15. Article
  16. Article
  17. Frontiers in oncology · 2021
    Article
  18. PDCD1 and IFNL4 genetic variants and risk of developing hepatitis C virus-related diseases.Liver international : official journal of the International Association for the Study of the Liver · 2021
    Article
  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.

Hong-Tao RenFrom the Departments of Oncology (H-TR, X-JW, H-FK, X-BM, X-HL, MW, KL, PX, Q-LY, Z-JD) and General Surgery (Y-ML), The Second Affiliated Hospital of Xi'an Jiaotong University; and National Engineering Research Center for Miniaturized Detection Systems, School of Life Sciences, Northwest University, Xi'an, China (T-BJ).
Yi-Ming Li
Xi-Jing Wang
Hua-Feng Kang
Tian-Bo Jin
Xiao-Bin Ma
Xing-Han Liu
Meng Wang
Kang Liu
Peng Xu
Qing-Ling Yao
Zhi-Jun Dai

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Programmed death-1 (PD-1) is crucial in cancer and is well characterized as a negative T-cell regulator that functions by delivering inhibitory signals. We aimed to evaluate the relationship between PD-1 polymorphisms (rs10204525, rs2227982, and rs7421861) and breast cancer risk.We selected 560 breast cancer patients and 583 age-, sex-, and ethnicity-matched healthy controls from Northwest China. The PD-1 polymorphisms were genotyped by using Sequenom MassARRAY. Associations were estimated with odds ratios (ORs) and 95% confidence intervals (95% CIs).For the rs10204525 and rs7421861 polymorphisms, no differences in breast cancer risk were found in any of the genetic models. For the rs2227982 polymorphism, the variant genotypes were significantly associated with decreased breast cancer risk (CT vs CC: OR = 0.68, 95% CI = 0.52-0.91; CT + TT vs CC: OR = 0.69, 95% CI = 0.53-0.90). In analyses stratified by age, the decreased risk was observed among the younger subjects (OR = 0.68, 95% CI = 0.47-0.97). We found that the decreased risk observed for the variant genotypes of rs2227982 was associated with the Her-2 status (CT vs CC: OR = 0.55, 95% CI = 0.37-0.84; CT + TT vs CC: OR = 0.56, 95% CI = 0.38-0.82). The haplotype analysis showed that the Ars10204525 Trs2227982 Crs7421861 haplotype was associated with a significantly decreased risk of breast cancer (OR = 0.50, 95% CI = 0.34-0.75).Our findings support an association between the PD-1 rs2227982 polymorphism and decreased breast cancer risk, especially in Her-2 positive breast cancer patients in the Chinese population.

Indexed as

AdultAge FactorsAllelesAsian PeopleBreast NeoplasmsCase-Control StudiesChinaErb-b2 Receptor Tyrosine KinasesFemaleGenetic Predisposition to DiseaseGenotypeHaplotypesHumansMiddle AgedPolymorphism, GeneticProgrammed Cell Death 1 ReceptorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesProgrammed Cell Death 1 Receptor

Identifiers

PMID27227944
PMCPMC4902368

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.