Evidence map›Paper›PMID 29445099›Full record

ArticleScientific reports2018

Pharmacokinetic-pharmacodynamic correlations in the development of ginger extract as an anticancer agent.

Rao Mukkavilli, Chunhua Yang, Reenu Singh Tanwar, Roopali Saxena, Sushma R Gundala, Yingyi Zhang, Ahmed Ghareeb, Stephan D Floyd, Subrahmanyam Vangala, Wei-Wen Kuo and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Potential Role of Ginger (Frontiers in nutrition · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. The Role of Curcumin in the Modulation of Ageing.International journal of molecular sciences · 2019
    Review
  17. Review
  18. 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

12 authors at 2 institutions in 2 countries.

Rao MukkavilliDepartment of Biology, Georgia State University, Atlanta, GA-30303, USA.
Chunhua YangDepartment of Biology, Georgia State University, Atlanta, GA-30303, USA.
Reenu Singh TanwarDepartment of Biology, Georgia State University, Atlanta, GA-30303, USA.
Roopali SaxenaDepartment of Biology, Georgia State University, Atlanta, GA-30303, USA.
Sushma R GundalaDepartment of Biology, Georgia State University, Atlanta, GA-30303, USA.
Yingyi ZhangDepartment of Biology, Georgia State University, Atlanta, GA-30303, USA.
Ahmed GhareebDepartment of Biology, Georgia State University, Atlanta, GA-30303, USA.
Stephan D FloydDepartment of Biology, Georgia State University, Atlanta, GA-30303, USA.
Subrahmanyam VangalaReaGene Biosciences Private Limited, Bengaluru, India.
Wei-Wen KuoDepartment of Biological Science and Technology, College of Biopharmaceutical and Food Sciences, China Medical University, Taichung, Taiwan, ROC.
Padmashree C G RidaDepartment of Biology, Georgia State University, Atlanta, GA-30303, USA.
Ritu AnejaDepartment of Biology, Georgia State University, Atlanta, GA-30303, USA. raneja@gsu.edu.
Georgia State University · USChina Medical University · TW

Funding

Evaluation of HSET as a Novel Theranostic Target for Breast Cancer TherapyR01CA169127 · NCI · GEORGIA STATE UNIVERSITY · PI ANEJA, RITU · 2012 to 2016
$1.7M
NCI NIH HHS R01 CA169127
6 · The paper itself

Abstract

Anticancer efficacy of ginger phenolics (GPs) has been demonstrated in various in vitro assays and xenograft mouse models. However, only sub-therapeutic plasma concentrations of GPs were detected in human and mouse pharmacokinetic (PK) studies. Intriguingly, a significant portion of GPs occurred as phase II metabolites (mainly glucuronide conjugates) in plasma. To evaluate the disposition of GPs and understand the real players responsible for efficacy, we performed a PK and tissue distribution study in mice. Plasma exposure of GPs was similar on day 1 and 7, suggesting no induction or inhibition of clearance pathways. Both free and conjugated GPs accumulated in all tissues including tumors. While non-cytotoxicity of 6-ginerol glucuronide precluded the role of conjugated GPs in cell death, the free forms were cytotoxic against prostate cancer cells. The efficacy of ginger was best explained by the reconversion of conjugated GPs to free forms by β-glucuronidase, which is over-expressed in the tumor tissue. This previously unrecognized two-step process suggests an instantaneous conversion of ingested free GPs into conjugated forms, followed by their subsequent absorption into systemic circulation and reconversion into free forms. This proposed model uncovers the mechanistic underpinnings of ginger's anticancer activity despite sub-therapeutic levels of free GPs in the plasma.

Indexed as

AnimalsAntineoplastic Agents, PhytogenicCatecholsCell Line, TumorCell ProliferationHumansMaleMiceMice, Inbred C57BLMice, NudePC-3 CellsPhenolsPlant ExtractsProstatic NeoplasmsXenograft Model Antitumor AssaysZingiber officinaleAntineoplastic Agents, PhytogenicCatecholsPhenolsPlant Extracts

Identifiers

PMID29445099
PMCPMC5813242
OpenAlexW2806483023

What OpenQuestion holds

Textmetadata
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.