Evidence map›Paper›PMID 27760163›Full record

ArticlePloS one2016

Role of PXR in Hepatic Cancer: Its Influences on Liver Detoxification Capacity and Cancer Progression.

Deepak Kotiya, Bharti Jaiswal, Sampa Ghose, Rachna Kaul, Kasturi Datta, Rakesh K Tyagi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.6field-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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Mechanisms and Therapeutic Advances of PXR in Metabolic Diseases and Cancer.International journal of molecular sciences · 2025
    Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
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  11. Article
  12. [Pregnane X receptor promotes programmed cell death protein 4 expression in HepG2 cells].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2020
    Article
  13. PXR: a center of transcriptional regulation in cancer.Acta pharmaceutica Sinica. B · 2020
    Review
  14. Evidence-based complementary and alternative medicine : eCAM · 2019
    Article
  15. Review
  16. Article
  17. 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 1 institution in 1 country.

Deepak KotiyaSpecial Centre for Molecular Medicine, Jawaharlal Nehru University, New Delhi, India.
Bharti JaiswalSpecial Centre for Molecular Medicine, Jawaharlal Nehru University, New Delhi, India.
Sampa GhoseSpecial Centre for Molecular Medicine, Jawaharlal Nehru University, New Delhi, India.
Rachna KaulSpecial Centre for Molecular Medicine, Jawaharlal Nehru University, New Delhi, India.
Kasturi DattaSpecial Centre for Molecular Medicine, Jawaharlal Nehru University, New Delhi, India.
Rakesh K TyagiSpecial Centre for Molecular Medicine, Jawaharlal Nehru University, New Delhi, India.
Jawaharlal Nehru University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of nuclear receptor PXR in detoxification and clearance of xenobiotics and endobiotics is well-established. However, its projected role in hepatic cancer is rather illusive where its expression is reported altered in different cancers depending on the tissue-type and microenvironment. The expression of PXR, its target genes and their biological or clinical significance have not been examined in hepatic cancer. In the present study, by generating DEN-induced hepatic cancer in mice, we report that the expression of PXR and its target genes CYP3A11 and GSTa2 are down-regulated implying impairment of hepatic detoxification capacity. A higher state of inflammation was observed in liver cancer tissues as evident from upregulation of inflammatory cytokines IL-6 and TNF-α along with NF-κB and STAT3. Our data in mouse model suggested a negative correlation between down-regulation of PXR and its target genes with that of higher expression of inflammatory proteins (like IL-6, TNF-α, NF-κB). In conjunction, our findings with relevant cell culture based assays showed that higher expression of PXR is involved in reduction of tumorigenic potential in hepatic cancer. Overall, the findings suggest that inflammation influences the expression of hepatic proteins important in drug metabolism while higher PXR level reduces tumorigenic potential in hepatic cancer.

Indexed as

Disease ProgressionInactivation, MetabolicAnimalsAntineoplastic AgentsBiotransformationCarcinogenesisCell Line, TumorCell Transformation, NeoplasticGene Expression Regulation, NeoplasticHumansLiverLiver NeoplasmsMaleMembrane Transport ProteinsMicePregnane X ReceptorAntineoplastic AgentsMembrane Transport ProteinsPregnane X ReceptorReceptors, Steroid

Identifiers

PMID27760163
PMCPMC5070842
OpenAlexW2537944038

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.