Evidence map›Paper›PMID 35002522›Full record

ReviewInternational journal of biological sciences2022

Insights into the critical role of the PXR in preventing carcinogenesis and chemotherapeutic drug resistance.

Xiaxia Niu, Ting Wu, Gege Li, Xinsheng Gu, Yanan Tian, Hongmei Cui

Open access · goldAbstract readReview
In one paragraph

Review in International journal of biological sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
1.8field-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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
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  13. Regulation of P-Glycoprotein during Oxidative Stress.Antioxidants (Basel, Switzerland) · 2024
    Review
  14. Review
  15. Natural medicinal compounds target signal transduction pathways to overcome ABC drug efflux transporter-mediated multidrug resistance in cancer.Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy · 2023
    Review
  16. Review
  17. Effects ofInternational journal of molecular sciences · 2022
    Article
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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.

Xiaxia NiuInstitute of Toxicology, School of Public Health, Lanzhou University, 730000, Lanzhou, China.
Ting WuInstitute of Toxicology, School of Public Health, Lanzhou University, 730000, Lanzhou, China.
Gege LiInstitute of Toxicology, School of Public Health, Lanzhou University, 730000, Lanzhou, China.
Xinsheng GuDepartment of Pharmacology, College of Basic Medical Sciences, Hubei University of Medicine, Shiyan 442000, Hubei, China.
Yanan TianDepartment of Veterinary Physiology and Pharmacology, Texas A&M University, USA.
Hongmei CuiInstitute of Toxicology, School of Public Health, Lanzhou University, 730000, Lanzhou, China.
Texas A&M University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pregnane x receptor (PXR) as a nuclear receptor is well-established in drug metabolism, however, it has pleiotropic functions in regulating inflammatory responses, glucose metabolism, and protects normal cells against carcinogenesis. Most studies focus on its transcriptional regulation, however, PXR can regulate gene expression at the translational level. Emerging evidences have shown that PXR has a broad protein-protein interaction network, by which is implicated in the cross signaling pathways. Furthermore, the interactions between PXR and some critical proteins (e.g., p53, Tip60, p300/CBP-associated factor) in DNA damage pathway highlight its potential roles in this field. A thorough understanding of how PXR maintains genome stability and prevents carcinogenesis will help clinical diagnosis and finally benefit patients. Meanwhile, due to the regulation of CYP450 enzymes CYP3A4 and multidrug resistance protein 1 (MDR1), PXR contributes to chemotherapeutic drug resistance. It is worthy of note that the co-factor of PXR such as RXRα, also has contributions to this process, which makes the PXR-mediated drug resistance more complicated. Although single nucleotide polymorphisms (SNPs) vary between individuals, the amino acid substitution on exon of PXR finally affects PXR transcriptional activity. In this review, we have summarized the updated mechanisms that PXR protects the human body against carcinogenesis, and major contributions of PXR with its co-factors have made on multidrug resistance. Furthermore, we have also reviewed the current promising antagonist and their clinic applications in reversing chemoresistance. We believe our review will bring insight into PXR-targeted cancer therapy, enlighten the future study direction, and provide substantial evidence for the clinic in future.

Indexed as

AnimalsATP Binding Cassette Transporter, Subfamily B, Member 1CarcinogenesisCytochrome P-450 CYP3ACytochrome P-450 Enzyme SystemDrug Resistance, NeoplasmGene Expression RegulationHumansNeoplasmsPeroxisome-Targeting Signal 1 ReceptorATP Binding Cassette Transporter, Subfamily B, Member 1Cytochrome P-450 CYP3ACytochrome P-450 Enzyme SystemPeroxisome-Targeting Signal 1 ReceptorPEX5 protein, humanchemotherapeutic drug resistancepost-translational modificationsPregnane nuclear receptor (PXR)protein-protein interactions

Identifiers

PMID35002522
PMCPMC8741843
OpenAlexW4200413271

What OpenQuestion holds

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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.