Evidence map›Paper›PMID 31223284›Full record

ArticleInternational journal of biological sciences2019

Nuclear CD44 Mediated by Importin β Participated in Naïve Genes Transcriptional Regulation in C3A-iCSCs.

Ming Su, Peipei Wang, Xuan Wang, Mingzhi Zhang, Shiruo Wei, Kaiyu Liu, Shuo Han, Xu Han, Yue Deng, Li Shen

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. CD44 as a tumor biomarker and therapeutic target.Experimental hematology & oncology · 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

10 authors at 3 institutions in 1 country.

Ming SuDepartment of Cell Biology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Peipei WangBeijing Cellonis Biotechnologies Co. Ltd, Zhongguancun Bio-Medicine Park, Beijing, People's Republic of China.
Xuan WangState Key Laboratory of Organ Failure Research, Co-Innovation Center for Organ Failure Research, Guangdong Provincial Southern Medical University, Guangzhou, Guangdong Province, 510515, China.
Mingzhi ZhangDepartment of Cell Biology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Shiruo WeiDepartment of Cell Biology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Kaiyu LiuState Key Laboratory of Organ Failure Research, Co-Innovation Center for Organ Failure Research, Guangdong Provincial Southern Medical University, Guangzhou, Guangdong Province, 510515, China.
Shuo HanMedical Center of Human Reproduction, Beijing Chaoyang Hospital, Capital Medical University, Beijing, 100069, China.
Xu HanState Key Laboratory of Organ Failure Research, Co-Innovation Center for Organ Failure Research, Guangdong Provincial Southern Medical University, Guangzhou, Guangdong Province, 510515, China.
Yue DengBeijing Cellonis Biotechnologies Co. Ltd, Zhongguancun Bio-Medicine Park, Beijing, People's Republic of China.
Li ShenDepartment of Cell Biology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Peking University · CNSouthern Medical University · CNCapital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD44 is one of biomarkers of liver cancer stem cells (CSCs). The investigation of mechanism of CD44 translocation helps to uncover new molecular pathways participated in the regulation of various cellular processes in CSCs. In the present study, we observed the translocation of CD44 from cytoplasm to nuclear in the reprogramming process of C3A cells, full-length CD44 presented in the nucleus of liver iCSCs. CD44 was bound with importin β and transportin 1 in liver iCSCs. Inhibition of importin β transport leads to reduction of CD44 in the nucleus. Translocation of CD44 is also influenced by importin α. Besides, overexpression of naïve pluripotent genes,

Indexed as

Active Transport, Cell Nucleusalpha Karyopherinsbeta KaryopherinsBiomarkersCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansHyaluronan ReceptorsLiver NeoplasmsNeoplastic Stem Cellsalpha Karyopherinsbeta KaryopherinsBiomarkersHyaluronan ReceptorsCD44importin βliver iCSCsnaïve gene

Identifiers

PMID31223284
PMCPMC6567805
OpenAlexW2947748141

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.