Evidence map›Paper›PMID 33144882›Full record

ArticleEcancermedicalscience2020

Screening of cytochrome 4Z1 expression in human non-neoplastic, pre-neoplastic and neoplastic tissues.

Yousef M Al-Saraireh, Nafea S Alboaisa, Hamzeh Mohammad Alrawashdeh, Omar Hamdan, Sameeh Al-Sarayreh, Jehad M Al-Shuneigat, Mohammad N Nofal

Open access · goldAbstract read
In one paragraph

Article in Ecancermedicalscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
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  9. Improved methods for the detection of heme and protoporphyrin IX adducts and quantification of heme B from cytochrome P450 containing systems.Journal of chromatography. B, Analytical technologies in the biomedical and life sciences · 2023
    Article
  10. Review
  11. Article
  12. Article
  13. Phytochemistry and Anticancer Effects of Mangrove (Pharmaceuticals (Basel, Switzerland) · 2022
    Article
  14. Article
  15. Human Orphan Cytochromes P450: An Update.Current drug metabolism · 2022
    Article
  16. Article
  17. Article
  18. Article
  19. 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

7 authors at 3 institutions in 2 countries.

Yousef M Al-SarairehDepartment of Pharmacology, Faculty of Medicine, University of Mutah, Karak 61710, Jordan.
Nafea S AlboaisaDepartment of Pathology, College of Medicine, University of Anbar, Baghdad 55431, 55 Ramadi.
Hamzeh Mohammad AlrawashdehDepartment of Ophthalmology, Ibn Al Haytham Hospital, Amman 410739, Jordan.
Omar HamdanDepartment of Pathology, College of Medicine, University of Mutah, Karak 61710, Jordan.
Sameeh Al-SarayrehDepartment of Biochemistry and Molecular Biology, Faculty of Medicine, University of Mutah, Karak 61710, Jordan.
Jehad M Al-ShuneigatDepartment of Biochemistry and Molecular Biology, Faculty of Medicine, University of Mutah, Karak 61710, Jordan.
Mohammad N NofalDepartment of General Surgery, Faculty of Medicine, University of Mutah, Karak 61710, Jordan.
Mutah University · JOJordan Hospital · JOUniversity of Anbar · IQ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCytochromes P450 (CYPs) constitute an enzyme family involved in the oxidative metabolism of a wide variety of endogenous and exogenous compounds, including anti-cancer drugs and carcinogens. Unlike other human CYPs, CYP4Z1 is highly expressed in human breast carcinoma and is associated with poor prognosis. As a result, CYP4Z1 was hypothesised to be a potential biomarker or drug target for the discovery and development of promising anti-cancer therapies. MATERIALS AND

methodsCYP4Z1 expression was immunohistochemically studied in a set of 100 different human tissues, including normal, benign, malignant and metastatic tissues, which originated from 27 anatomical sites. As a tumour model for CYP4Z1 expression, a panel of different breast cancers was evaluated for CYP4Z1 expression and its relation to histopathological features and prognostic immunohistochemical markers.

resultsThe immunohistochemical results revealed that CYP4Z1 was expressed in only one (4.3%) of the normal tissues from the mammary glands, while the expression of the enzyme was positive in 1 (11%), 12 (19%) and 2 (40%) of the benign, malignant and metastatic tissues, respectively. Interestingly, several tumour entities showed prominent expressions of CYP4Z1, including carcinomas of adrenal cortex, squamous cells of oesophagus, lung and cervix, as well as seminoma, astrocytoma, melanoma and lastly endometrial adenocarcinoma. In breast cancers, CYP4Z1 was expressed in 82% of the cases. Its expression was significantly associated with the pathology of tumour, histological grade and status of lymph node metastasis. Importantly, it was also significantly associated with the expressions of Her2, P53 and Ki-67.

conclusionThese findings greatly support future plans for the use of CYP4Z1 as a biomarker or target for anti-cancer drugs. However, large-scale validation studies are needed to better delineate the potential use of CYP4Z1 for therapeutic purposes.

Indexed as

breast cancercancerCYP4Z1cytochrome P450immunohistochemistry

Identifiers

PMID33144882
PMCPMC7581338
OpenAlexW3089904342

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Registered trials

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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.