Evidence map›Paper›PMID 29068672›Full record

ArticleChemical research in toxicology2017

Effects of Black Raspberry Extract and Berry Compounds on Repair of DNA Damage and Mutagenesis Induced by Chemical and Physical Agents in Human Oral Leukoplakia and Rat Oral Fibroblasts.

Joseph B Guttenplan, Kun-Ming Chen, Yuan-Wan Sun, Braulio Lajara, Nora A E Shalaby, Wieslawa Kosinska, Gabrielle Benitez, Krishne Gowda, Shantu Amin, Gary Stoner and 1 more

Open access · greenAbstract read
In one paragraph

Article in Chemical research in toxicology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
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  7. Review
  8. Review
  9. Article
  10. Effects of the Tobacco CarcinogensChemical research in toxicology · 2019
    Article
  11. Effects of Black Raspberry on Dibenzo[Cancer prevention research (Philadelphia, Pa.) · 2018
    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

11 authors at 2 institutions in 1 country.

Joseph B GuttenplanDepartment of Basic Science, New York University College of Dentistry , New York, New York 10010, United States.ORCID 0000-0002-8873-9349
Kun-Ming Chen
Yuan-Wan Sun
Braulio LajaraDepartment of Basic Science, New York University College of Dentistry , New York, New York 10010, United States.
Nora A E ShalabyDepartment of Basic Science, New York University College of Dentistry , New York, New York 10010, United States.
Wieslawa KosinskaDepartment of Basic Science, New York University College of Dentistry , New York, New York 10010, United States.
Gabrielle Benitez
Krishne Gowda
Shantu Amin
Gary StonerDepartment of Medicine, Medical College of Wisconsin , Milwaukee, Wisconsin 53226, United States.
New York University · USMedical College of Wisconsin · US

Funding

Chemoprevention by Black Raspberry of Oral Cancer Induced by Tobacco Carcinogens: Translational StudiesR01CA173465 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI EL-BAYOUMY, KARAM E · 2013 to 2024
$3.1M
NCI NIH HHS R01 CA173465
6 · The paper itself

Abstract

Black raspberries (BRB) have been shown to inhibit carcinogenesis in a number of systems, with most studies focusing on progression. Previously we reported that an anthocyanin-enriched black raspberry extract (BE) enhanced repair of dibenzo-[a,l]-pyrene dihydrodiol (DBP-diol)-induced DNA adducts and inhibited DBP-diol and DBP-diolepoxide (DBPDE)-induced mutagenesis in a lacI rat oral fibroblast cell line, suggesting a role for BRB in the inhibition of initiation of carcinogenesis. Here we extend this work to protection by BE against DNA adduct formation induced by dibenzo-[a,l]-pyrene (DBP) in a human oral leukoplakia cell line (MSK) and to a second carcinogen, UV light. Treatment of MSK cells with DBP and DBPDE led to a dose-dependent increase in DBP-DNA adducts. Treatment of MSK cells with BE after addition of DBP reduced levels of adducts relative to cells treated with DBP alone, and treatment of rat oral fibroblasts with BE after addition of DBPDE inhibited mutagenesis. These observations showed that BE affected repair of DNA adducts and not metabolism of DBP. As a proof of principle we also tested aglycones of two anthocyanins commonly found in berries, delphinidin chloride and pelargonidin chloride. Delphinidin chloride reduced DBP-DNA adduct levels in MSK cells, while PGA did not. These results suggested that certain anthocyanins can enhance repair of bulky DNA adducts. As DBP and its metabolites induced formation of bulky DNA adducts, we investigated the effects of BE on genotoxic effects of a second carcinogen that induces bulky DNA damage, UV light. UV irradiation produced a dose-dependent increase in cyclobutanepyrimidine dimer levels in MSK cells, and post-UV treatment with BE resulted in lower cyclobutanepyrimidine dimer levels. Post-UV treatment of the rat lacI cells with BE reduced UV-induced mutagenesis. Taken together, the results demonstrate that BE extract reduces bulky DNA damage and mutagenesis and support a role for BRB in the inhibition of initiation of carcinogenesis.

Indexed as

AnimalsBenzopyrenesCells, CulturedDNADNA AdductsDNA DamageDose-Response Relationship, DrugFibroblastsHumansLeukoplakia, OralMiceMolecular StructurePlant ExtractsRatsRubusStructure-Activity RelationshipBenzopyrenesdibenzo(a,l)pyreneDNADNA AdductsPlant Extracts

Identifiers

PMID29068672
PMCPMC7880227
OpenAlexW2766784056

What OpenQuestion holds

Textmetadata
LicenceTDM
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.