Evidence map›Paper›PMID 28048942›Full record

ArticleMolecular pharmaceutics2017

Therapeutic Efficacy of a Family of pHLIP-MMAF Conjugates in Cancer Cells and Mouse Models.

Kelly E Burns, Harvey Hensley, Matthew K Robinson, Damien Thévenin

Abstract read
In one paragraph

Article in Molecular pharmaceutics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. Article
  3. Next-generation agents for fluorescence-guided glioblastoma surgery.Bioengineering & translational medicine · 2024
    Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Research advances in peptide‒drug conjugates.Acta pharmaceutica Sinica. B · 2023
    Review
  10. Anti-Cancer Peptides: Status and Future Prospects.Molecules (Basel, Switzerland) · 2023
    Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  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

4 authors.

Kelly E BurnsDepartment of Chemistry, Lehigh University , 6 East Packer Avenue, Bethlehem, Pennsylvania 18015, United States.
Harvey HensleyMolecular Therapeutics Program, Fox Chase Cancer Center , 333 Cottman Avenue, Philadelphia, Pennsylvania 19111, United States.
Matthew K RobinsonMolecular Therapeutics Program, Fox Chase Cancer Center , 333 Cottman Avenue, Philadelphia, Pennsylvania 19111, United States.
Damien ThéveninDepartment of Chemistry, Lehigh University , 6 East Packer Avenue, Bethlehem, Pennsylvania 18015, United States.ORCID 0000-0002-1866-0694

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Dietmar J Kappes · 1985 to 2026
$138.8M
Selective Delivery of Monomethyl Auristatin Derivatives to Prostate Tumors UsingR21CA181868 · NCI · LEHIGH UNIVERSITY · PI ROBINSON, MATTHEW K, THEVENIN, DAMIEN · 2014 to 2015
$421k
NCI NIH HHS P30 CA006927NCI NIH HHS R21 CA181868
6 · The paper itself

Abstract

The targeting of therapeutics specifically to diseased tissue is crucial for the development of successful cancer treatments. The approach here is based on the pH(low) insertion peptide (pHLIP) for the delivery of a potent mitotic inhibitor monomethyl auristatin F (MMAF). We investigated six pHLIP variants conjugated to MMAF to compare their efficacy in vitro against cultured cancer cells. While all pHLIP-MMAF conjugates exhibit potent pH- and concentration-dependent killing, their cytotoxicity profiles are remarkably different. We also show that the lead conjugate exhibits significant therapeutic efficacy in mouse models without overt toxicities. This study confirms pHLIP-monomethyl auristatin conjugates as possible new therapeutic options for cancer treatment and supports their further development.

Indexed as

AminobenzoatesAnimalsAntibodies, MonoclonalAntineoplastic AgentsCell LineCell Line, TumorFemaleHeLa CellsHumansHydrogen-Ion ConcentrationImmunoconjugatesMiceMice, NudeOligopeptidesPeptidesAminobenzoatesAntibodies, MonoclonalAntineoplastic AgentsauristatinImmunoconjugatesOligopeptidesPeptidescytotoxicityin vivo efficacymonomethyl auristatinspeptide drug deliverytargeted drug deliverytumor acidity

Identifiers

PMID28048942
PMCPMC5293657

What Socratic holds

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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 Socratic graph.