Evidence map›Paper›PMID 26513297›Full record

ArticleOncotarget2015

CUDR promotes liver cancer stem cell growth through upregulating TERT and C-Myc.

Hu Pu, Qidi Zheng, Haiyan Li, Mengying Wu, Jiahui An, Xin Gui, Tianming Li, Dongdong Lu

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

49 citing papers in PubMed, 80 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. The emerging landscape of long non-coding RNAs in hepatocellular carcinoma.International journal of clinical and experimental pathology · 2021
    Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Dual Effects of Non-Coding RNAs (ncRNAs) in Cancer Stem Cell Biology.International journal of molecular sciences · 2020
    Review
  15. Article
  16. The Dynamic Chromatin Architecture of the Regenerating Liver.Cellular and molecular gastroenterology and hepatology · 2020
    Article
  17. Overexpression of NNT-AS1 Activates TGF-BioMed research international · 2020
    Article
  18. Review
  19. Article
  20. Emerging Roles of Long non-coding RNAs in The Tumor Microenvironment.International journal of biological sciences · 2020
    Review
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 1 institution in 1 country.

Hu PuSchool of Life Science and Technology, Tongji University, Shanghai 200092, China.
Qidi ZhengSchool of Life Science and Technology, Tongji University, Shanghai 200092, China.
Haiyan LiSchool of Life Science and Technology, Tongji University, Shanghai 200092, China.
Mengying WuSchool of Life Science and Technology, Tongji University, Shanghai 200092, China.
Jiahui AnSchool of Life Science and Technology, Tongji University, Shanghai 200092, China.
Xin GuiSchool of Life Science and Technology, Tongji University, Shanghai 200092, China.
Tianming LiSchool of Life Science and Technology, Tongji University, Shanghai 200092, China.
Dongdong LuSchool of Life Science and Technology, Tongji University, Shanghai 200092, China.
Tongji University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer up-regulated drug resistant (CUDR) is a novel non-coding RNA gene. Herein, we demonstrate excessive CUDR cooperates with excessive CyclinD1 or PTEN depletion to accelerate liver cancer stem cells growth and liver stem cell malignant transformation in vitro and in vivo. Mechanistically, we reveal the decrease of PTEN in cells may lead to increase binding capacity of CUDR to CyclinD1. Therefore, CUDR-CyclinD1 complex loads onto the long noncoding RNA H19 promoter region that may lead to reduce the DNA methylation on H19 promoter region and then to enhance the H19 expression. Strikingly, the overexpression of H19 increases the binding of TERT to TERC and reduces the interplay between TERT with TERRA, thus enhancing the cell telomerase activity and extending the telomere length. On the other hand, insulator CTCF recruits the CUDR-CyclinD1 complx to form the composite CUDR-CyclinD1-insulator CTCF complex which occupancied on the C-myc gene promoter region, increasing the outcome of oncogene C-myc. Ultimately, excessive TERT and C-myc lead to liver cancer stem cell and hepatocyte-like stem cell malignant proliferation. To understand the novel functions of long noncoding RNA CUDR will help in the development of new liver cancer therapeutic and diagnostic approaches.

Indexed as

AnimalsApoptosisBlotting, WesternCarcinoma, HepatocellularCell ProliferationCell Transformation, NeoplasticChromatin ImmunoprecipitationGene Expression Regulation, NeoplasticHumansImmunoprecipitationIn Situ HybridizationLiver NeoplasmsMaleMiceMice, Inbred BALB CMice, NudeMYC protein, humanProto-Oncogene Proteins c-mycRNA, Long NoncodingRNA, MessengerTelomeraseTERT protein, humanUCA1 RNA, humanCUDRliver cancer stem cellPTEN

Identifiers

PMID26513297
PMCPMC4747368
OpenAlexW2270778366

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.