Evidence map›Paper›PMID 26409826›Full record

ArticleBMC genomics2015

Integrative genomics analysis of genes with biallelic loss and its relation to the expression of mRNA and micro-RNA in esophageal squamous cell carcinoma.

Nan Hu, Chaoyu Wang, Robert J Clifford, Howard H Yang, Hua Su, Lemin Wang, Yuan Wang, Yi Xu, Ze-Zhong Tang, Ti Ding and 5 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

25 citing papers in PubMed, 50 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Cancers · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  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

15 authors at 5 institutions in 2 countries.

Nan HuGenetic Epidemiology Branch, DCEG, NCI, 9609 Medical Center Drive, Rm 6E444 MSC 9769, Bethesda, MD, 20892-9769, USA. nhu@nih.gov.
Chaoyu WangGenetic Epidemiology Branch, DCEG, NCI, 9609 Medical Center Drive, Rm 6E444 MSC 9769, Bethesda, MD, 20892-9769, USA. wangc@mail.nih.gov.
Robert J CliffordHigh-dimension Data Analysis Group, Basic Research Laboratory, Center for Cancer Research, 9609 Medical Center Drive, Rm 1W586, Bethesda, MD, 20892, USA. robert.j.clifford21.ctr@mail.mil.
Howard H YangHigh-dimension Data Analysis Group, Basic Research Laboratory, Center for Cancer Research, 9609 Medical Center Drive, Rm 1W586, Bethesda, MD, 20892, USA. hy43h@nih.gov.
Hua SuGenetic Epidemiology Branch, DCEG, NCI, 9609 Medical Center Drive, Rm 6E444 MSC 9769, Bethesda, MD, 20892-9769, USA. suhu@mail.nih.gov.
Lemin WangGenetic Epidemiology Branch, DCEG, NCI, 9609 Medical Center Drive, Rm 6E444 MSC 9769, Bethesda, MD, 20892-9769, USA. wangl4@mail.nih.gov.
Yuan WangShanxi Cancer Hospital, Taiyuan, Shanxi, 030013, People's Republic of China. zmkt_z@yeah.net.
Yi XuShanxi Cancer Hospital, Taiyuan, Shanxi, 030013, People's Republic of China. zmkt_z@yeah.net.
Ze-Zhong TangShanxi Cancer Hospital, Taiyuan, Shanxi, 030013, People's Republic of China. zmkt_z@yeah.net.
Ti DingShanxi Cancer Hospital, Taiyuan, Shanxi, 030013, People's Republic of China. zmkt_z@yeah.net.
Tongwu ZhangLaboratory of Translational Genomics, DCEG, NCI, Bethesda, MD, 20892, USA. tongwu.zhang@nih.gov.
Alisa M GoldsteinGenetic Epidemiology Branch, DCEG, NCI, 9609 Medical Center Drive, Rm 6E444 MSC 9769, Bethesda, MD, 20892-9769, USA. ag26o@nih.gov.
Carol GiffenInformation Management Services, Inc., Silver Spring, Bethesda, MD, 20904, USA. giffenc@imsweb.com.
Maxwell P LeeHigh-dimension Data Analysis Group, Basic Research Laboratory, Center for Cancer Research, 9609 Medical Center Drive, Rm 1W586, Bethesda, MD, 20892, USA. leemax@mail.nih.gov.
Philip R TaylorGenetic Epidemiology Branch, DCEG, NCI, 9609 Medical Center Drive, Rm 6E444 MSC 9769, Bethesda, MD, 20892-9769, USA. ptaylor@mail.nih.gov.
Shanxi Provincial Cancer Hospital · CNAnalysis Group (United States) · USCenter for Cancer Research · USID Genomics (United States) · USInformation Management Services · US

Funding

Esophageal cancer genetic projectZIACP010224 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI GOLDSTEIN, ALISA · 2012 to 2025
$7.3M
Intramural NIH HHS
6 · The paper itself

Abstract

backgroundGenomic instability plays an important role in human cancers. We previously characterized genomic instability in esophageal squamous cell carcinomas (ESCC) in terms of loss of heterozygosity (LOH) and copy number (CN) changes in tumors. In the current study we focus on biallelic loss and its relation to expression of mRNA and miRNA in ESCC using results from 500 K SNP, mRNA, and miRNA arrays in 30 cases from a high-risk region of China.

results(i) Biallelic loss was uncommon but when it occurred it exhibited a consistent pattern: only 77 genes (<0.5%) showed biallelic loss in at least 10% of ESCC samples, but nearly all of these genes were concentrated on just four chromosomal arms (i.e., 42 genes on 3p, 14 genes on 9p, 10 genes on 5q, and seven genes on 4p). (ii) Biallelic loss was associated with lower mRNA expression: 52 of the 77 genes also had RNA expression data, and 41 (79%) showed lower expression levels in cases with biallelic loss compared to those without. (iii) The relation of biallelic loss to miRNA expression was less clear but appeared to favor higher miRNA levels: of 60 miRNA-target gene pairs, 34 pairs (57%) had higher miRNA expression with biallelic loss than without, while 26 pairs (43%) had lower miRNA expression. (iv) Finally, the effect of biallelic loss on the relation between miRNA and mRNA expression was complex. Biallelic loss was most commonly associated with a pattern of elevated miRNA and reduced mRNA (43%), but a pattern of both reduced miRNA and mRNA was also common (35%).

conclusionOur results indicate that biallelic loss in ESCC is uncommon, but when it occurs it is localized to a few specific chromosome regions and is associated with reduced mRNA expression of affected genes. The effect of biallelic loss on miRNA expression and on the relation between miRNA and mRNA expressions was complex.

Indexed as

Genetic Association StudiesAdultAgedAllelesCarcinoma, Squamous CellChinaChromosomes, HumanEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaFemaleGenomic InstabilityHumansMaleMicroRNAsMiddle AgedNeoplasm GradingMicroRNAsRNA, Messenger

Identifiers

PMID26409826
PMCPMC4584010
OpenAlexW2148243390

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.