Evidence map›Paper›PMID 16786358›Full record

ArticleJournal of cancer research and clinical oncology2006

The membrane-cytoskeleton organizer ezrin is necessary for hepatocellular carcinoma cell growth and invasiveness.

Yan Zhang, Mei-Yu Hu, Wei-Zhong Wu, Zhi-Jun Wang, Kang Zhou, Xi-Liang Zha, Kang-Da Liu

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Expression and significance of Six1 and Ezrin in cervical cancer tissue.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2011
    Article
  13. Expression change of ezrin as a prognostic factor in primary osteosarcoma.Medical oncology (Northwood, London, England) · 2011
    Article
  14. Expression of ezrin in human embryonic, fetal, and normal adult tissues.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2011
    Article
  15. Article
  16. Proteomic analysis of differentially expressed proteins in peripheral cholangiocarcinoma.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2010
    Article
  17. Article
  18. Article
  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

7 authors at 3 institutions in 1 country.

Yan ZhangExperimental Center of Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Mei-Yu Hu
Wei-Zhong Wu
Zhi-Jun Wang
Kang Zhou
Xi-Liang Zha
Kang-Da Liu
Fudan University · CNZhongshan Hospital · CNFudan University Shanghai Cancer Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe change of cell mobility is one of the preconditions of tumor metastasis. Cell skeleton alteration and rearrangement of F-actin was closely related to cell mobility. Ezrin is a membrane-cytoskeleton organizer that can mediate the rearrangement and the function of F-actin. In this paper, we investigated the effect of ezrin on hepatocellular carcinoma cell growth and invasiveness.

methodsHepatocellular carcinoma cell lines such as MHCC-1, MHCC97-H, SF7721, SMMC7721, Hep3B, and HepG2 were chosen in this study. We first examined the expression and the distribution of ezrin and F-actin in these cell lines using immunofluorescence, RT-PCR, and the western blot. Next we used small interfering RNA (siRNA) to down-regulate ezrin expression in MHCC-1, MHCC97-H, SF7721, and HepG2 to investigate the role of ezrin in tumor cell growth and invasiveness.

resultsOur preliminary results showed that the expression of ezrin and gamma-actin in MHCC-1, MHCC97-H, and SF7721 with higher metastatic potential were obviously up-regulated than those in SMMC7721, Hep3B, and HepG2 with lower potential. No different expression of beta-actin was found in the above tumor cell lines. The outcome of RNAi indicated that decreasing ezrin expression can notably inhibit the proliferation of the four hepatocellular carcinoma cell lines (p < 0.01, n = 10). The proportion of cells in G2-M phase also decreased after RNAi. The number of pseudopods decreased as well after RNAi treatment (p < 0.01, n = 5). The mobility and invasiveness of cancer cells decreased with decreasing ezrin expression tested by transwell assay (p < 0.01, n = 8).

conclusionEzrin plays an important role in the process of hepatocellular carcinoma cell proliferation, migration, and invasiveness.

Indexed as

Cell ProliferationActinsApoptosisBlotting, WesternCarcinoma, HepatocellularCell DivisionCell MembraneCytoskeletal ProteinsCytoskeletonEzrinFluorescent Antibody TechniqueG2 PhaseHumansLiver NeoplasmsNeoplasm InvasivenessPseudopodiaActinsCytoskeletal ProteinsEzrinRNA, Small Interfering

Identifiers

PMID16786358
PMCPMC12161023
OpenAlexW2012953879

What OpenQuestion holds

Textmetadata
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.