Evidence map›Paper›PMID 40646362›Full record

ReviewCurrent microbiology2025

Optimizing Gene Sources for L-asparaginase Production: A Comparative Review.

Vida Ebrahimi, Atieh Hashemi

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Vida EbrahimiDepartment of Pharmaceutical Biotechnology, School of Pharmacy, Shahid Beheshti University of Medical Sciences, No. 2660, Valiasr-Niayesh Junction, Vali-E-Asr Ave, Tehran, 19968-35113, Iran.ORCID http://orcid.org/0000-0003-3920-5073
Atieh HashemiDepartment of Pharmaceutical Biotechnology, School of Pharmacy, Shahid Beheshti University of Medical Sciences, No. 2660, Valiasr-Niayesh Junction, Vali-E-Asr Ave, Tehran, 19968-35113, Iran. at_hashemi@sbmu.ac.ir.ORCID http://orcid.org/0000-0001-7121-5306

Funding

Shahid Beheshti University of Medical Sciences IR.SBMU.PHARMACY.REC.1402.025
6 · The paper itself

Abstract

L-asparaginase is a versatile enzyme that has been a vital tool in both cancer treatment and food production. In the clinic, it's used as a first-line treatment for acute lymphoblastic leukemia. That's because it can deplete the extracellular L-asparagine that cancer cells need to multiply. In the food industry, it helps reduce the formation of acrylamide in starchy foods that are cooked at high heat. That makes food safer for consumers. The enzyme's performance depends heavily on where its genes come from. That source affects how well it works, how stable it is, how likely it is to trigger an immune response-and how feasible it is to produce. To evaluate the best gene sources for L-asparaginase, this review scoured the major biomedical databases. It fills a gap in existing research by systematically assessing gene sources based on their suitability for different applications: cancer therapy, food safety and biosensing. By matching gene selection with the needs of downstream applications, this review shows how application-driven gene sourcing can lead to safer, more effective and more viable L-asparaginase variants. That approach gives us new insights to guide the next generation of biotech and clinical advancements in enzyme design and deployment.

Indexed as

AsparaginaseBacteriaHumansAsparaginase

Identifiers

What OpenQuestion holds

Textmetadata
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.