Evidence map›Paper›PMID 26259033›Full record

ArticleNature medicine2015

Retrotransposon insertions in the clonal evolution of pancreatic ductal adenocarcinoma.

Nemanja Rodić, Jared P Steranka, Alvin Makohon-Moore, Allison Moyer, Peilin Shen, Reema Sharma, Zachary A Kohutek, Cheng Ran Huang, Daniel Ahn, Paolo Mita and 6 more

Abstract read
In one paragraph

Article in Nature medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
39.3field-weighted citation impact, top 1% 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

92 citing papers in PubMed, 153 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Revisiting Clonal Evolution Through the Light of Retrotransposons.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  5. Current issues in molecular biology · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Transposons disrupt genomic stability and trigger cancers.Frontiers in cellular and infection microbiology · 2025
    Review
  13. Article
  14. Regulation and function of transposable elements in cancer genomes.Cellular and molecular life sciences : CMLS · 2024
    Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Article

32 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 1 country.

Nemanja RodićDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Jared P SterankaDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Alvin Makohon-MooreDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Allison MoyerDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Peilin ShenDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Reema SharmaDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Zachary A KohutekDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Cheng Ran HuangMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Daniel AhnDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Paolo MitaDepartment of Molecular Biology &Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Martin S TaylorHigh Throughput (HiT) Biology Center, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Norman J BarkerDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Ralph H HrubanDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Christine A Iacobuzio-DonahueDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Jef D BoekeMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Kathleen H BurnsDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Johns Hopkins Medicine · USJohns Hopkins University · USHigh Throughput Biology (United States) · USMemorial Sloan Kettering Cancer Center · US

Funding

Tumor Antigens for Individual Signatures and TherapyP50CA062924 · NCI · JOHNS HOPKINS UNIVERSITY · PI LENNON, ANNE MARIE · 1993 to 2022
$54.6M
Predoctoral Training Program in Human GeneticsT32GM007814 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI VALLE, DAVID · 1985 to 2021
$10.6M
Training CoreP50GM107632 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BOEKE, JEF D · 2013 to 2017
$10.0M
Transposon Insertion Polymorphisms in Predispositions to Hematopoietic NeoplasiaR01CA163705 · NCI · JOHNS HOPKINS UNIVERSITY · PI BURNS, KATHLEEN H · 2013 to 2017
$1.7M
(PQB6) Genetics of Subclonal Evolution in Pancreatic CancerR01CA179991 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI IACOBUZIO-DONAHUE, CHRISTINE A · 2013 to 2016
$1.3M
Mouse Models of Functional Insertion PolymorphismsR01GM103999 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI BURNS, KATHLEEN H · 2013 to 2016
$1.2M
Retrotransposon instability in glioblastoma multiformeR01CA161210 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BOEKE, JEF D · 2011 to 2014
$1.1M
Subclonal Evolution in Metastatic Pancreatic CancerF31CA180682 · NCI · JOHNS HOPKINS UNIVERSITY · PI MAKOHON-MOORE, ALVIN · 2013 to 2014
$74k
NCI NIH HHS F31 CA180682NCI NIH HHS F31CA180682NCI NIH HHS P50 CA062924NCI NIH HHS P50CA62924NCI NIH HHS R01 CA161210NCI NIH HHS R01 CA163705NCI NIH HHS R01CA163705NCI NIH HHS R01 CA179991NCI NIH HHS R01CA179991NIGMS NIH HHS P50 GM107632NIGMS NIH HHS P50GM107632NIGMS NIH HHS R01 GM103999NIGMS NIH HHS R01GM103999NIGMS NIH HHS T32 GM007814
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is typically diagnosed after the disease has metastasized; it is among the most lethal forms of cancer. We recently described aberrant expression of an open reading frame 1 protein, ORF1p, encoded by long interspersed element-1 (LINE-1; L1) retrotransposon, in PDAC. To test whether LINE-1 expression leads to somatic insertions of this mobile DNA, we used a targeted method to sequence LINE-1 insertion sites in matched PDAC and normal samples. We found evidence of 465 somatic LINE-1 insertions in 20 PDAC genomes, which were absent from corresponding normal samples. In cases in which matched normal tissue, primary PDAC and metastatic disease sites were available, insertions were found in primary and metastatic tissues in differing proportions. Two adenocarcinomas secondarily involving the pancreas, but originating in the stomach and duodenum, acquired insertions with a similar discordance between primary and metastatic sites. Together, our findings show that LINE-1 contributes to the genetic evolution of PDAC and suggest that somatic insertions are acquired discontinuously in gastrointestinal neoplasms.

Indexed as

Clonal EvolutionApoptotic Protease-Activating Factor 1Carcinoma, Pancreatic DuctalHumansLong Interspersed Nucleotide ElementsPancreatic NeoplasmsAPAF1 protein, humanApoptotic Protease-Activating Factor 1

Identifiers

PMID26259033
PMCPMC4775273
OpenAlexW1176330553

What OpenQuestion holds

Textmetadata
LicenceTDM
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.