Evidence map›Paper›PMID 27203676›Full record

ArticleOncotarget2016

Significant change of cytochrome P450s activities in patients with hepatocellular carcinoma.

Jun Zhou, Qiang Wen, Sai-Fei Li, Yun-Fei Zhang, Na Gao, Xin Tian, Yan Fang, Jie Gao, Ming-Zhu Cui, Xiao-Pei He and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
9.4field-weighted citation impact, top 2% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 87 citations in OpenAlex.

  1. Pooled it
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  12. Role of p53 suppression in the pathogenesis of hepatocellular carcinoma.World journal of gastrointestinal pathophysiology · 2023
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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

13 authors at 2 institutions in 1 country.

Jun ZhouInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, People's Republic of China.
Qiang WenInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, People's Republic of China.
Sai-Fei LiHenan Provincal People's Hospital, Zhengzhou, People's Republic of China.
Yun-Fei ZhangInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, People's Republic of China.
Na GaoInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, People's Republic of China.
Xin TianInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, People's Republic of China.
Yan FangInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, People's Republic of China.
Jie GaoInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, People's Republic of China.
Ming-Zhu CuiHenan Provincal People's Hospital, Zhengzhou, People's Republic of China.
Xiao-Pei HeInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, People's Republic of China.
Lin-Jing JiaInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, People's Republic of China.
Han JinInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, People's Republic of China.
Hai-Ling QiaoInstitute of Clinical Pharmacology, Zhengzhou University, Zhengzhou, People's Republic of China.
Zhengzhou University · CNZhengzhou People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The lack of information concerning individual variation in drug-metabolizing enzymes is one of the most important obstacles for designing personalized medicine approaches for hepatocellular carcinoma (HCC) patients. To assess cytochrome P450 (CYP) in the metabolism of endogenous and exogenous molecules in an HCC setting, the activity changes of 10 major CYPs in microsomes from 105 normal and 102 HCC liver tissue samples were investigated. We found that CYP activity values expressed as intrinsic clearance (CLint) differed between HCC patients and control subjects. HCC patient samples showed increased CLint for CYP2C9, CYP2D6, and CYP2E1 compared to controls. Meanwhile, CYP1A2, CYP2C8, and CYP2C19 CLint values decreased and CYP2A6, CYP2B6, and CYP3A4/5 activity was unchanged relative to controls. For patients with HCC accompanied by fibrosis or cirrhosis, the same activity changes were seen for the CYP isoforms, except for CYP2D6 which had higher values in HCC patients with cirrhosis. Moreover, CYP2D6*10 (100C>T), CYP2C9*3 (42614 A>C), and CYP3A5*3 (6986A>G) polymorphisms had definite effects on enzyme activities. In the HCC group, the CLint of CYP2D6*10 mutant homozygote was decreased by 95% compared to wild-type samples, and the frequency of this homozygote was 2.8-fold lower than the controls.In conclusion, the activities of CYP isoforms were differentially affected in HCC patients. Genetic polymorphisms of some CYP enzymes, especially CYP2D6*10, could affect enzyme activity. CYP2D6*10 allelic frequency was significantly different between HCC patients and control subjects. These findings may be useful for personalizing the clinical treatment of HCC patients as well as predicting the risk of hepatocarcinogenesis.

Indexed as

AdultAgedCarcinoma, HepatocellularCytochrome P-450 CYP2C9Cytochrome P-450 CYP2D6Cytochrome P-450 CYP2E1Cytochrome P-450 CYP3ACytochrome P-450 Enzyme SystemFemaleFibrosisGene FrequencyGenotypeHomozygoteHumansLiverLiver NeoplasmsCytochrome P-450 CYP2C9Cytochrome P-450 CYP2D6Cytochrome P-450 CYP2E1Cytochrome P-450 CYP3ACytochrome P-450 Enzyme Systemcytochrome P450drug metabolismgene polymorphismhepatocellular carcinomahuman liver microsomes

Identifiers

PMID27203676
PMCPMC5226607
OpenAlexW2395532827

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.