Evidence map›Paper›PMID 31754084›Full record

ArticleAging2019

p62-DNA-encoding plasmid reverts tumor grade, changes tumor stroma, and enhances anticancer immunity.

Franco M Venanzi, Vladimir Gabai, Francesca Mariotti, Gian Enrico Magi, Cecilia Vullo, Albert A Sufianov, Sergey I Kolesnikov, Alexander Shneider

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Recombinant probioticFrontiers in microbiology · 2024
    Article
  6. Review
  7. Review
  8. p62: Friend or Foe? Evidences forInternational journal of molecular sciences · 2020
    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

8 authors at 4 institutions in 4 countries.

Franco M VenanziSechenov First Moscow State Medical University, Moscow, Russia.
Vladimir GabaiCureLab Oncology, Inc, Deadham, MA 02026, USA.
Francesca MariottiSchool of Biosciences and Veterinary Medicine, University of Camerino, Camerino, Italy.
Gian Enrico MagiSchool of Biosciences and Veterinary Medicine, University of Camerino, Camerino, Italy.
Cecilia VulloSchool of Biosciences and Veterinary Medicine, University of Camerino, Camerino, Italy.
Albert A SufianovSechenov First Moscow State Medical University, Moscow, Russia.
Sergey I KolesnikovRussian Academy of Sciences, Moscow, Russia.
Alexander ShneiderSechenov First Moscow State Medical University, Moscow, Russia.
Sechenov University · RUUniversità di Camerino · ITBoston University · USLomonosov Moscow State University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previously, we reported that the administration of a p62/SQSTM1-encoding plasmid demonstrates high safety and signs of clinical benefits for human cancer patients. The treatment also suppressed tumor growth and metastasis in dogs and mouse models. Here we investigated some mechanistic aspects of these effects. In mammary tumors bearing-dogs, i.m. injections of p62 plasmid reduced tumor sizes and their aggressive potential in 5 out of 6 animals, with one carcinoma switching to adenoma. The treatment increased levels of smooth muscle actin in stroma cells and type III collagen in the extracellular matrix, which correlate with a good clinical prognosis. The p62 treatment also increased the abundance of intratumoral T-cells. Because of the role of adaptive immunity cannot be tested in dogs, we compared the protective effects of the p62 plasmid against B16 melanoma in wild type C57BL/6J mice versus their SCID counterpart lacking lymphocytes. The plasmid was only protective in the wild type strain. Also, p62 plasmid amplified the anti-tumor effect of T-cell transfer from tumor-bearing animals to animals challenged with the same tumors. We conclude that the plasmid acts via re-modeling of the tumor microenvironment, making it more favorable for increased anti-cancer immunity. Thus, the p62-encoding plasmid might be a new adjuvant for cancer treatments.

Indexed as

Genetic TherapyMammary Neoplasms, ExperimentalSequestosome-1 ProteinTumor MicroenvironmentAnimalsDogsFemaleGenetic VectorsMelanoma, ExperimentalMiceMice, Inbred C57BLMice, SCIDPlasmidsSequestosome-1 ProteinSQSTM1 protein, humananti-cancer immunitycanine tumorsDNA plasmidp62 /SQSTM1tumor microenvironment

Identifiers

PMID31754084
PMCPMC6914433
OpenAlexW2990253966

What OpenQuestion holds

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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.