Evidence map›Paper›PMID 28100395›Full record

ArticleeLife2017

Replication Study: Coadministration of a tumor-penetrating peptide enhances the efficacy of cancer drugs.

Christine Mantis, Irawati Kandela, Fraser Aird, Reproducibility Project: Cancer Biology

Abstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
–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

25 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Exosomal targeting and its potential clinical application.Drug delivery and translational research · 2022
    Review
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  7. Review
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  11. Article
  12. On the low reproducibility of cancer studies.National science review · 2018
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Overcoming key biological barriers to cancer drug delivery and efficacy.Journal of controlled release : official journal of the Controlled Release Society · 2017
    Review
  19. Targeted drug delivery using iRGD peptide for solid cancer treatment.Molecular systems design & engineering · 2017
    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

4 authors.

Christine MantisDevelopmental Therapeutics Core, Northwestern University, Evanston, United States.
Irawati KandelaDevelopmental Therapeutics Core, Northwestern University, Evanston, United States.
Fraser AirdDevelopmental Therapeutics Core, Northwestern University, Evanston, United States.
Reproducibility Project: Cancer Biology

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In 2015, as part of the Reproducibility Project: Cancer Biology, we published a Registered Report (Kandela et al., 2015) that described how we intended to replicate selected experiments from the paper "Coadministration of a tumor-penetrating peptide enhances the efficacy of cancer drugs" (Sugahara et al., 2010). Here we report the results of those experiments. We found that coadministration with iRGD peptide did not have an impact on permeability of the chemotherapeutic agent doxorubicin (DOX) in a xenograft model of prostate cancer, whereas the original study reported that it increased the penetrance of this cancer drug (Figure 2B; Sugahara et al., 2010). Further, in mice bearing orthotopic 22Rv1 human prostate tumors, we did not find a statistically significant difference in tumor weight for mice treated with DOX and iRGD compared to DOX alone, whereas the original study reported a decrease in tumor weight when DOX was coadministered with iRGD (Figure 2C; Sugahara et al., 2010). In addition, we did not find a statistically significant difference in TUNEL staining in tumor tissue between mice treated with DOX and iRGD compared to DOX alone, while the original study reported an increase in TUNEL positive staining with iRGD coadministration (Figure 2D; Sugahara et al., 2010). Similar to the original study (Supplemental Figure 9A; Sugahara et al., 2010), we did not observe an impact on mouse body weight with DOX and iRGD treatment. Finally, we report meta-analyses for each result.

Indexed as

AnimalsAntineoplastic Combined Chemotherapy ProtocolsCell Line, TumorDoxorubicinDrug Delivery SystemsHumansLiposomesMaleMicePeptidesProstatic NeoplasmsReproducibility of ResultsTumor BurdenXenograft Model Antitumor AssaysDoxorubicinLiposomesPeptidescancer biologydoxorubicinhumanmetasciencemousereplicationreproducibilityReproducibility Project: Cancer Biologytumor penetrating peptide

Identifiers

PMID28100395
PMCPMC5245960

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.