Evidence map›Paper›PMID 23531335›Full record

ArticleJournal of hematology & oncology2013

Lynch syndrome related endometrial cancer: clinical significance beyond the endometrium.

Yiying Wang, Yue Wang, Jie Li, Janiel Cragun, Kenneth Hatch, Setsuko K Chambers, Wenxin Zheng

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Journal of hematology & oncology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05257057 (Frequency of Endometrial Cancer Precursors Associated with Lynch Syndrome), which is not on this map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.6field-weighted citation impact, top 11% 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.

NCT05257057 completednot on this mapstarted 2019, after this paper: background citation

Frequency of Endometrial Cancer Precursors Associated with Lynch Syndrome

TypeobservationalSponsorWellSpan HealthRan2019 to 2023Enrolled91ConditionsLynch Syndrome, Endometrial Cancer, Endometrial Hyperplasia, Mismatch Repair DeficiencyArmsImmunohistochemical staining
3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. circRNAs in Endometrial Cancer-A Promising Biomarker: State of the Art.International journal of molecular sciences · 2024
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Diagnostics of Mutations in MMR/Diagnostics (Basel, Switzerland) · 2020
    Review
  14. Article
  15. Review
  16. Review
  17. Cancer management and research · 2020
    Article
  18. 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

7 authors at 3 institutions in 2 countries.

Yiying WangDepartment of Obstetrics and Gynecology, Henan Province People’s Hospital Zhengzhou, Henan, China.
Yue Wang
Jie Li
Janiel Cragun
Kenneth Hatch
Setsuko K Chambers
Wenxin Zheng
University of Arizona · USHenan Provincial People's Hospital · CNQilu Hospital of Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lynch syndrome (LS), an autosomal dominant inherited cancer susceptibility syndrome, also known as hereditary non-polyposis colon cancer (HNPCC), is caused by a germline mutation in one of several DNA mismatch repair (MMR) genes. LS is the most common presentation of hereditary colorectal cancer (CRC), accounting for about 2-5% of all CRC cases. More recently, it is found that a similar number of endometrial cancers is also due to one of the MMR gene mutations. There has been significant progress in LS-related CRC in terms of molecular pathogenesis, risks, genetic basis, and cancer prevention. In contrast, the advance about LS-related endometrial cancer (EC) is very much limited. In this commentary, we summarize the main clinicopathologic features of LS-related EC and propose universal screening for LS in individuals with endometrial cancer.

Indexed as

Genetic TestingColorectal Neoplasms, Hereditary NonpolyposisEndometrial NeoplasmsFemaleHumansPrognosis

Identifiers

PMID23531335
PMCPMC3623651
OpenAlexW2122079027

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.