Evidence map›Paper›PMID 23461856›Full record

ArticleThe FEBS journal2013

Cancer stem-like cell properties are regulated by EGFR/AKT/β-catenin signaling and preferentially inhibited by gefitinib in nasopharyngeal carcinoma.

Lei Ma, Gong Zhang, Xiao-Bo Miao, Xu-Bin Deng, Yue Wu, Ying Liu, Zhi-Ru Jin, Xi-Qing Li, Qiu-Zhen Liu, Du-Xin Sun and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The FEBS journal, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

54 citing papers in PubMed, 93 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Knockdown ofCell adhesion & migration · 2023
    Article
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  7. Article
  8. International journal of molecular sciences · 2022
    Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Nimotuzumab plus platinum-based chemotherapyTherapeutic advances in medical oncology · 2020
    Article
  15. Review
  16. 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

13 authors at 3 institutions in 2 countries.

Lei Ma *Cancer Institute, Southern Medical University, Guangzhou, China.
Gong Zhang *Cancer Institute, Southern Medical University, Guangzhou, China.
Xiao-Bo MiaoCancer Institute, Southern Medical University, Guangzhou, China.
Xu-Bin DengCancer Institute, Southern Medical University, Guangzhou, China.
Yue WuCancer Institute, Southern Medical University, Guangzhou, China.
Ying LiuCancer Institute, Southern Medical University, Guangzhou, China.
Zhi-Ru JinCancer Institute, Southern Medical University, Guangzhou, China.
Xi-Qing LiCancer Institute, Southern Medical University, Guangzhou, China.
Qiu-Zhen LiuCancer Institute, Southern Medical University, Guangzhou, China.
Du-Xin SunDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Michigan, Ann Arbor, MI, USA.
Joseph R TestaFox Chase Cancer Center, Philadelphia, USA.
Kai-Tai YaoCancer Institute, Southern Medical University, Guangzhou, China.
Guang-Hui XiaoCancer Institute, Southern Medical University, Guangzhou, China.
Southern Medical University · CNFox Chase Cancer Center · USUniversity of Michigan–Ann Arbor · US

Funding

Basis for Lymphomagenesis in Akt2 Transgenic MiceR01CA077429 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI TESTA, JOSEPH R. · 1998 to 2013
$4.7M
NCI NIH HHS CA77429NCI NIH HHS R01 CA077429
6 · The paper itself

Abstract

We report that the epidermal growth factor receptor (EGFR) pathway plays a critical role in regulating cancer stem-like cells (CSCs) in nasopharyngeal carcinoma (NPC), one of the most common malignant tumors in Southeast Asia. Effects of EGFR on maintaining CSCs are mainly mediated by AKT signaling, and β-catenin is responsible for governing CSC properties in response to EGFR/AKT activation. Significantly, CSCs are enriched by cisplatin and decreased by gefitinib in NPC xenograft models. Upon reimplantation in secondary mice, tumor cells derived from cisplatin-treated mice grew rapidly, whereas regrowth of tumor cells from gefitinib-treated mice was severely diminished. We further demonstrate that expression of EGFR correlates with expression of β-catenin and Nanog in primary tumor specimens from NPC patients. These findings provide mechanistic and preclinical evidence supporting the use of gefitinib alone or in combination with a chemotherapeutic agent in first-line therapy for patients with NPC. In addition, our results suggest that targeting β-catenin represents a rational clinical modality for patients whose tumors harbor activated EGFR or AKT.

Indexed as

Signal TransductionAnimalsAntineoplastic Agentsbeta CateninCarcinomaCell Line, TumorCell ProliferationCell SurvivalCell Transformation, NeoplasticCisplatinErbB ReceptorsGefitinibGene Knockdown TechniquesHomeodomain ProteinsHumansMiceAntineoplastic Agentsbeta CateninCisplatinErbB ReceptorsGefitinibHomeodomain ProteinsNanog Homeobox ProteinNANOG protein, humanProto-Oncogene Proteins c-aktQuinazolines

Identifiers

PMID23461856
PMCPMC3831031
OpenAlexW1988890456

What OpenQuestion holds

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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.