Evidence map›Paper›PMID 27371094›Full record

ArticleJournal of experimental & clinical cancer research : CR2016

Enhanced therapeutic effect of an antiangiogenesis peptide on lung cancer in vivo combined with salmonella VNP20009 carrying a Sox2 shRNA construct.

Changhong Zhao, Junjin He, Haoran Cheng, Zhaohao Zhu, Hanmei Xu

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.7field-weighted citation impact, top 12% 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

27 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
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  3. Biomedicines · 2025
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  7. Non-pathogenic Trojan horseMaterials today. Bio · 2024
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  8. Bacterial live therapeutics for human diseases.Molecular systems biology · 2024
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  11. Attenuated mutants ofExperimental biology and medicine (Maywood, N.J.) · 2024
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  13. Acta biochimica et biophysica Sinica · 2023
    Review
  14. Article
  15. Frontiers in cellular and infection microbiology · 2023
    Review
  16. Pharmaceutics · 2022
    Review
  17. Recombinant AttenuatedCancers · 2022
    Review
  18. Review
  19. Review
  20. Integration ofCancers · 2021
    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

5 authors at 1 institution in 1 country.

Changhong ZhaoThe Engineering Research Center of Peptide Drug Discovery and Development, China Pharmaceutical University, 24 Tongjia Xiang, Nanjing, 210009, People's Republic of China.
Junjin HeThe Engineering Research Center of Peptide Drug Discovery and Development, China Pharmaceutical University, 24 Tongjia Xiang, Nanjing, 210009, People's Republic of China.
Haoran ChengThe Engineering Research Center of Peptide Drug Discovery and Development, China Pharmaceutical University, 24 Tongjia Xiang, Nanjing, 210009, People's Republic of China.
Zhaohao ZhuThe Engineering Research Center of Peptide Drug Discovery and Development, China Pharmaceutical University, 24 Tongjia Xiang, Nanjing, 210009, People's Republic of China.
Hanmei XuThe Engineering Research Center of Peptide Drug Discovery and Development, China Pharmaceutical University, 24 Tongjia Xiang, Nanjing, 210009, People's Republic of China. 13913925346@126.com.
China Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHM-3 is a polypeptide inhibiting angiogenesis. Recent reports suggest that the antitumor effect of angiogenesis inhibitors administered alone might be limited. Cancer stem cells can survive the lack of oxygen and nutrients. To achieve better anti-tumor effect, HM-3 was administered in combination with the attenuated Salmonella typhimurium VNP20009 transformed with a shRNA construct against sex determining region Y-box 2 (Sox2).

methodsCell invasion assay and soft agar colony formation assay were used to assess the migration and growth capability of A549 cells once Sox2 was knocked down with the shRNA construct. The shRNA construct targeting Sox2 was transformed into VNP20009. After the mouse xenograft model of A549 was established, HM-3 was co-administered with VNP20009 carrying the shRNA construct. The growth of tumor was checked to compare the effectiveness of different therapies. Western blotting assay and immunohistochemistry staining of the tumor tissue were used to measure the levels of proteins associated with the apoptosis pathway.

resultsSox2 was necessary for the migration and growth of A549 cells. The expression of Sox2 was down regulated in the tumor tissue of the combined treatment group of HM-3 with VNP20009 carrying the Sox2 shRNA construct. Together with the accumulation of salmonella in tumor and the inhibition of angiogenesis by HM-3, more tumor cells went through cell apoptosis with increased expression of Bax, cleaved Caspase 3 and decreased expression of Bcl2.

conclusionsThe results suggest the combination of antiangiogenesis agent HM-3 with gene therapy targeting Sox2 delivered by salmonella as a promising strategy for the treatment of lung cancer.

Indexed as

A549 CellsAngiogenesis InhibitorsAnimalsApoptosis Regulatory ProteinsBacterial VaccinesCell Line, TumorCell MovementCell ProliferationCell SurvivalCombined Modality TherapyGene Expression Regulation, NeoplasticHumansLung NeoplasmsMicePeptidesRNA, Small InterferingAngiogenesis InhibitorsApoptosis Regulatory ProteinsBacterial VaccinesPeptidesRNA, Small InterferingSOX2 protein, humanSOXB1 Transcription FactorsVNP 20009AntiangiogenesisApoptosisLung cancerSalmonella typhimuriumSox2

Identifiers

PMID27371094
PMCPMC4930618
OpenAlexW2467799941

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.