Evidence map›Paper›PMID 27446500›Full record

ArticleTheranostics2016

RGD Peptide Cell-Surface Display Enhances the Targeting and Therapeutic Efficacy of Attenuated Salmonella-mediated Cancer Therapy.

Seung-Hwan Park, Jin Hai Zheng, Vu Hong Nguyen, Sheng-Nan Jiang, Dong-Yeon Kim, Michael Szardenings, Jung Hyun Min, Yeongjin Hong, Hyon E Choy, Jung-Joon Min

Abstract read
In one paragraph

Article in Theranostics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
–field-weighted citation impact
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

90 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Deletion of themBio · 2026
    Article
  6. Review
  7. Review
  8. Living Microbial Drugs.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026
    Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. AttenuatedFrontiers in immunology · 2026
    Review
  17. Article
  18. Optimization Strategies and Synergistic Applications of EngineeredInternational journal of nanomedicine · 2026
    Review
  19. Review
  20. Review

30 more citing papers are in PubMed but not listed here.

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.

Seung-Hwan Park1. Department of Nuclear Medicine, Chonnam National University Medical School, Gwangju, Republic of Korea;; 6. Biological Resource Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Jeongeup, Republic of Korea.
Jin Hai Zheng1. Department of Nuclear Medicine, Chonnam National University Medical School, Gwangju, Republic of Korea;
Vu Hong Nguyen1. Department of Nuclear Medicine, Chonnam National University Medical School, Gwangju, Republic of Korea;
Sheng-Nan Jiang3. Department of Nuclear Medicine, Haikou Hospital Affiliated to Xiangya School of Medicine, Central South University, China;
Dong-Yeon Kim1. Department of Nuclear Medicine, Chonnam National University Medical School, Gwangju, Republic of Korea;
Michael Szardenings4. Fraunhofer IZI, Leipzig, Germany;
Jung Hyun Min5. Department of Biology, Kyung Hee University College of Science, Seoul, Republic of Korea;
Yeongjin Hong2. Department of Microbiology, Chonnam National University Medical School, Gwangju, Republic of Korea;
Hyon E Choy2. Department of Microbiology, Chonnam National University Medical School, Gwangju, Republic of Korea;
Jung-Joon Min1. Department of Nuclear Medicine, Chonnam National University Medical School, Gwangju, Republic of Korea;; 2. Department of Microbiology, Chonnam National University Medical School, Gwangju, Republic of Korea;

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacteria-based anticancer therapies aim to overcome the limitations of current cancer therapy by actively targeting and efficiently removing cancer. To achieve this goal, new approaches that target and maintain bacterial drugs at sufficient concentrations during the therapeutic window are essential. Here, we examined the tumor tropism of attenuated Salmonella typhimurium displaying the RGD peptide sequence (ACDCRGDCFCG) on the external loop of outer membrane protein A (OmpA). RGD-displaying Salmonella strongly bound to cancer cells overexpressing αvβ3, but weakly bound to αvβ3-negative cancer cells, suggesting the feasibility of displaying a preferential homing peptide on the bacterial surface. In vivo studies revealed that RGD-displaying Salmonellae showed strong targeting efficiency, resulting in the regression in αvβ3-overexpressing cancer xenografts, and prolonged survival of mouse models of human breast cancer (MDA-MB-231) and human melanoma (MDA-MB-435). Thus, surface engineering of Salmonellae to display RGD peptides increases both their targeting efficiency and therapeutic effect.

Indexed as

Cell Surface Display TechniquesDrug CarriersAnimalsAntineoplastic AgentsBacterial AdhesionBacterial Outer Membrane ProteinsBreast NeoplasmsDisease Models, AnimalHeterograftsHumansIntegrin alphaVbeta3MelanomaMiceOligopeptidesRecombinant Fusion ProteinsSalmonella typhimuriumAntineoplastic Agentsarginyl-glycyl-aspartic acidBacterial Outer Membrane ProteinsDrug CarriersIntegrin alphaVbeta3OligopeptidesOMPA outer membrane proteinsRecombinant Fusion Proteinsbacteria-mediated cancer therapybioluminescence imaging.RGD peptideSalmonella typhimuriumsurface display

Identifiers

PMID27446500
PMCPMC4955065

What OpenQuestion holds

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Registered trials

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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.