Evidence map›Paper›PMID 30755640›Full record

ArticleScientific reports2019

Prognostic nomogram of hypoxia-related genes predicting overall survival of colorectal cancer-Analysis of TCGA database.

Joon-Hyop Lee, Sohee Jung, Won Seo Park, Eun Kyung Choe, Eunyoung Kim, Rumi Shin, Seung Chul Heo, Jae Hyun Lee, Kwangsoo Kim, Young Jun Chai

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
–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

38 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. CuPCA: a web server for pan-cancer association analysis of large-scale cuproptosis-related genes.Database : the journal of biological databases and curation · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

10 authors.

Joon-Hyop LeeDepartment of Surgery, Gachon University College of Medicine, Gil Medical Center, Incheon, Republic of Korea.ORCID 0000-0003-0470-7719
Sohee JungDivision of Clinical Bioinformatics, Biomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0003-0596-7926
Won Seo ParkDepartment of Surgery, Kyung Hee University Hospital, Seoul, Republic of Korea.
Eun Kyung ChoeDepartment of Surgery, Seoul National University Hospital Healthcare System, Gangnam Center, Seoul, Republic of Korea.
Eunyoung KimDepartment of Surgery, National Medical Center, Seoul, Republic of Korea.
Rumi ShinDepartment of Surgery, Seoul Metropolitan Government, Seoul National University Boramae Medical Center, Seoul, Republic of Korea.
Seung Chul HeoDepartment of Surgery, Seoul Metropolitan Government, Seoul National University Boramae Medical Center, Seoul, Republic of Korea.
Jae Hyun LeeDepartment of Statistics, Korea University, Seoul, Republic of Korea.
Kwangsoo KimDivision of Clinical Bioinformatics, Biomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea. kksoo@snuh.org.
Young Jun ChaiDepartment of Surgery, Seoul Metropolitan Government, Seoul National University Boramae Medical Center, Seoul, Republic of Korea. kevinjoon@naver.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypoxia-related gene (HRG) expression is associated with survival outcomes of colorectal cancer (CRC). Our aim was developing a nomogram predicting CRC overall survival (OS) with HRGs and clinicopathological factors. The Cancer Genome Atlas (TCGA) database was used as discovery cohort and two Gene Expression Omnibus databases (GSE39582 and GSE41258) served as validation cohorts. A genetic risk score model prognosticating OS was developed using mRNA expression level of HRGs. Nomogram predicting OS was developed using genetic risk score model and clinicopathological variables. The genetic risk score model included four HRGs (HSPA1L, PUM1, UBE2D2, and HSP27) and successfully prognosticated OS of discovery and two validation cohorts (p < 0.001 for TCGA discovery set, p < 0.003 for the GSE39582 and p = 0.042 for the GSE41258 datasets). Nomogram included genetic risk score, age, and TNM stage. Harrell's concordance indexes of the nomogram were higher than those of TNM stage alone in the discovery set (0.77 vs. 0.69, p < 0.001), GSE39582 (0.65 vs. 0.63, p < 0.001), and GSE41258 datasets (0.78 vs. 0.77, p < 0.001). Our nomogram successfully predicted OS of CRC patients. The mRNA expression level of the HRGs might be useful as an ancillary marker for prognosticating CRC outcome.

Indexed as

Databases, FactualAgedColorectal NeoplasmsFemaleHumansMaleMiddle AgedNomogramsPrognosisProportional Hazards ModelsRisk FactorsRNA, MessengerRNA, Messenger

Identifiers

PMID30755640
PMCPMC6372658

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.