Evidence map›Paper›PMID 21170807›Full record

ArticleJournal of toxicology and environmental health. Part B, Critical reviews2010

Metabolism, genotoxicity, and carcinogenicity of comfrey.

Nan Mei, Lei Guo, Peter P Fu, James C Fuscoe, Yang Luan, Tao Chen

Open access · greenAbstract read
In one paragraph

Article in Journal of toxicology and environmental health. Part B, Critical reviews, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Ethnopharmacological insights intoFrontiers in pharmacology · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Comprehensive safety evaluation ofFrontiers in nutrition · 2025
    Article
  8. Review
  9. Advancing botanical safety: A strategy for selecting, sourcing, and characterizing botanicals for developing toxicological tools.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2024
    Article
  10. HPLC-HESI-MS/MS Analysis of Phenolic Compounds fromPlants (Basel, Switzerland) · 2024
    Article
  11. Article
  12. Article
  13. Rumen Metabolism ofJournal of agricultural and food chemistry · 2022
    Article
  14. Article
  15. Review
  16. Genotoxicity of Water Extract from Bark-RemovedMolecules (Basel, Switzerland) · 2021
    Article
  17. Evaluation of pyrrolizidine alkaloid-induced genotoxicity using metabolically competent TK6 cell lines.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2020
    Article
  18. Article
  19. Molecules (Basel, Switzerland) · 2019
    Review
  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

6 authors at 3 institutions in 3 countries.

Nan MeiDivision of Genetic and Reproductive Toxicology, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, Arkansas 72079, USA. nan.mei@fda.hhs.gov
Lei Guo
Peter P Fu
James C Fuscoe
Yang Luan
Tao Chen
Biochemical Society · GBUnited States Food and Drug Administration · USShanghai Institute of Materia Medica · CN

Funding

Intramural FDA HHS FD999999
6 · The paper itself

Abstract

Comfrey has been consumed by humans as a vegetable and a tea and used as an herbal medicine for more than 2000 years. Comfrey, however, produces hepatotoxicity in livestock and humans and carcinogenicity in experimental animals. Comfrey contains as many as 14 pyrrolizidine alkaloids (PA), including 7-acetylintermedine, 7-acetyllycopsamine, echimidine, intermedine, lasiocarpine, lycopsamine, myoscorpine, symlandine, symphytine, and symviridine. The mechanisms underlying comfrey-induced genotoxicity and carcinogenicity are still not fully understood. The available evidence suggests that the active metabolites of PA in comfrey interact with DNA in liver endothelial cells and hepatocytes, resulting in DNA damage, mutation induction, and cancer development. Genotoxicities attributed to comfrey and riddelliine (a representative genotoxic PA and a proven rodent mutagen and carcinogen) are discussed in this review. Both of these compounds induced similar profiles of 6,7-dihydro-7-hydroxy-1-hydroxymethyl-5H-pyrrolizine (DHP)-derived DNA adducts and similar mutation spectra. Further, the two agents share common mechanisms of drug metabolism and carcinogenesis. Overall, comfrey is mutagenic in liver, and PA contained in comfrey appear to be responsible for comfrey-induced toxicity and tumor induction.

Indexed as

AnimalsCarcinogensComfreyHumansLiverMutagensPlant PreparationsPyrrolizidine AlkaloidsRatsCarcinogensMutagensPlant PreparationsPyrrolizidine Alkaloids

Identifiers

PMID21170807
PMCPMC5894094
OpenAlexW1998693962

What OpenQuestion holds

Textmetadata
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.