Evidence map›Paper›PMID 36380291›Full record

ArticleClinical proteomics2022

Functional and quantitative evaluation of the 20S proteasome in serum and intracellular in145 moroccan patients with hematologic malignancies.

Hassan Filali, Ouadie Mohamed El Yaagoubi, Ayoub Lahmadi, Asmaa Quessar, Said El Antri, Hamid Samaki, Souad Aboudkhil

Open access · goldAbstract read
In one paragraph

Article in Clinical proteomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. 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

7 authors at 2 institutions in 1 country.

Hassan FilaliLaboratory of Biochemistry, Environment and Agrifood (URAC 36), Faculty of Science and Technology, Mohammedia-University Hassan II of Casablanca, Mohammedia, Morocco. filali_hassan@hotmail.fr.
Ouadie Mohamed El YaagoubiLaboratory of Biochemistry, Environment and Agrifood (URAC 36), Faculty of Science and Technology, Mohammedia-University Hassan II of Casablanca, Mohammedia, Morocco. ouadie.elyaagoubi@gmail.com.
Ayoub LahmadiLaboratory of Biochemistry, Environment and Agrifood (URAC 36), Faculty of Science and Technology, Mohammedia-University Hassan II of Casablanca, Mohammedia, Morocco.
Asmaa QuessarHematology and Pediatric Oncology Service-Hospital August 20, UniversityHospital Center IBN ROCHD Casablanca, Casablanca, Morocco.
Said El AntriLaboratory of Biochemistry, Environment and Agrifood (URAC 36), Faculty of Science and Technology, Mohammedia-University Hassan II of Casablanca, Mohammedia, Morocco.
Hamid SamakiNational Institute of Social Actions (INAS), Tanger, Morocco.
Souad AboudkhilLaboratory of Biochemistry, Environment and Agrifood (URAC 36), Faculty of Science and Technology, Mohammedia-University Hassan II of Casablanca, Mohammedia, Morocco.
Université Hassan II Mohammedia · MACentre Hospitalier Universitaire Ibn Rochd · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRegulatory degradation of intracellular proteins plays an essential role in most biological processes, particularly in the control of cell proliferation and differentiation. In eukaryotes, intracellular proteolysis is largely provided by the Ubiquitin / Proteasome system. Alterations and dysfunction of protein degradation by the Ubiquitin / Proteasome system, such as transcription factors, cell cycle regulators or tumor suppressor proteins, have been linked to human. Pathologies, including blood cancers. Mainly localized in the nucleus and cytoplasm of cells, the proteasome can be detected in the cell culture supernatant or in the peripheral blood of patients. This study deals with the problems of the search for serum markers specific to certain pathologies and which would be useful in the prevention, diagnosis and monitoring of cancers and which could be used as a therapeutic tool.

methodsThe functional and quantitative analysis of the proteasome is carried out at the serum and subcellular level during a pathological phenomenon in a population of 145 Moroccan patients (sex ratio: 1.10 / average age: 47.9 ± 15, 3 years) using an indirect ELISA test and a follow-up of the fluorescence emitted after enzymatic digestion of specific peptides by proteolytic activity (chymotrypsin-like).

resultsThe evolutionary trend proteasome subcellular is significantly linked to the rate of chymotrypsin-like activity. The entire population of 60 patients called back for a second blood test. After three months of treatment reported a significant drop in the rate and the activity of the proteasome in serum and intracellular level.

conclusionsAlthough the serum proteasome level is a potential new tool for the monitoring of. Patientswithliquid cancer.

trial registrationretrospectively registered.

Indexed as

Chymotrypsin-likeactivityELISA AssayHematologic malignanciesProteasome

Identifiers

PMID36380291
PMCPMC9664591
OpenAlexW4309192643

What OpenQuestion holds

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LicenceCC BY
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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.