Evidence map›Paper›PMID 28157704›Full record

ArticleOncotarget2017

Overlooked FANCD2 variant encodes a promising, portent tumor suppressor, and alternative polyadenylation contributes to its expression.

Bing Han, Yihang Shen, Piyan Zhang, Panneerselvam Jayabal, Raymond Che, Jun Zhang, Herbert Yu, Peiwen Fei

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Focal Point of Fanconi Anemia Signaling.International journal of molecular sciences · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Multifaceted Fanconi Anemia Signaling.Trends in genetics : TIG · 2018
    Review
  18. Article
  19. Fanconi Anemia Signaling and Cancer.Trends in cancer · 2017
    Review
  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

8 authors at 4 institutions in 1 country.

Bing HanUniversity of Hawaii Cancer Center, University of Hawaii, Honolulu, HI, USA.
Yihang ShenUniversity of Hawaii Cancer Center, University of Hawaii, Honolulu, HI, USA.
Piyan ZhangDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Panneerselvam JayabalUniversity of Hawaii Cancer Center, University of Hawaii, Honolulu, HI, USA.
Raymond CheUniversity of Hawaii Cancer Center, University of Hawaii, Honolulu, HI, USA.
Jun ZhangDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Herbert YuUniversity of Hawaii Cancer Center, University of Hawaii, Honolulu, HI, USA.
Peiwen FeiUniversity of Hawaii Cancer Center, University of Hawaii, Honolulu, HI, USA.
University of Hawaii System · USMayo Clinic in Arizona · USUniversity of Hawaiʻi at Mānoa · USUniversity of Hawaii Cancer Center

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Molecular Insights into the Fanconi Anemia Tumor Suppressor Signaling PathwayR01CA188251 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI FEI, PEIWEN · 2014 to 2018
$1.6M
NCATS NIH HHS UL1 TR001863NCI NIH HHS R01 CA188251
6 · The paper itself

Abstract

Fanconi Anemia (FA) complementation group D2 protein (FANCD2) is the center of the FA tumor suppressor pathway, which has become an important field of investigation in human aging and cancer. Here we report an overlooked central player in the FA pathway, FANCD2 variant 2 (FANCD2-V2), which appears to perform more potent tumor suppressor-function compared to the known variant of FANCD2, namely, FANCD2-V1. Detailed analysis of the FANCD2 gene structure indicated a proximal and distal polyadenylation site (PAS), associated with V2 and V1 transcripts accordingly. RNA polymerase II Chromatin immunoprecipitation (ChIP) targeting the two PAS-regions determined lesser binding of RNA pol II to DNA fragments in the distal PAS region in non-malignant cells compared to malignant cells. Conversely, the opposite occurred in the proximal PAS region. Moreover, RNA immunoprecipitation (RIP) identified that U2 snRNP, a major component of RNA splicing complex that interacts with the 3'end of an intron, showed greater binding to the last intron of the FANCD2-V1 transcript in malignant cells compared to the non-malignant cells. Importantly, our data showed that in human tissue samples, the ratio of V2 /V1 expression in lung, bladder, or ovarian cancer correlates inversely with the tumor stages/grades. Therefore, these findings provide a previously unrecognized central player FANCD2-V2 and thus novel insights into human tumorigenesis, and indicate that V2/V1 can act as an effective biomarker in assisting the recognition of tumor malignance.

Indexed as

Alternative SplicingBiomarkers, TumorCarcinogenesisFanconi AnemiaFanconi Anemia Complementation Group D2 ProteinFemaleGene Expression RegulationHumansLung NeoplasmsNeoplasm StagingOvarian NeoplasmsPolyadenylationTranscriptomeTumor Suppressor ProteinsUrinary Bladder NeoplasmsBiomarkers, TumorFANCD2 protein, humanFanconi Anemia Complementation Group D2 ProteinTumor Suppressor ProteinsFANCD2FANCD2-V1fanconi anemiapolyadenylation site (PAS)tumor suppressor

Identifiers

PMID28157704
PMCPMC5410239
OpenAlexW2585874015

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.