Evidence map›Paper›PMID 38999958›Full record

ArticleInternational journal of molecular sciences2024

Integrating In Silico and In Vitro Approaches to Identify Natural Peptides with Selective Cytotoxicity against Cancer Cells.

Hui-Ju Kao, Tzu-Han Weng, Chia-Hung Chen, Yu-Chi Chen, Yu-Hsiang Chi, Kai-Yao Huang, Shun-Long Weng

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
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.

Hui-Ju KaoDepartment of Medical Research, Hsinchu MacKay Memorial Hospital, Hsinchu City 300, Taiwan.
Tzu-Han WengDepartment of Dermatology, MacKay Memorial Hospital, Taipei City 104, Taiwan.
Chia-Hung ChenDepartment of Medical Research, Hsinchu MacKay Memorial Hospital, Hsinchu City 300, Taiwan.
Yu-Chi ChenDepartment of Medical Research, Hsinchu MacKay Memorial Hospital, Hsinchu City 300, Taiwan.
Yu-Hsiang ChiNational Center for High-Performance Computing, Hsinchu City 300, Taiwan.
Kai-Yao HuangDepartment of Medical Research, Hsinchu MacKay Memorial Hospital, Hsinchu City 300, Taiwan.
Shun-Long WengDepartment of Medicine, MacKay Medical College, New Taipei City 252, Taiwan.

Funding

National Science and Technology Council, R.O.C NSTC 112-2221-E-195-002
6 · The paper itself

Abstract

Anticancer peptides (ACPs) are bioactive compounds known for their selective cytotoxicity against tumor cells via various mechanisms. Recent studies have demonstrated that in silico machine learning methods are effective in predicting peptides with anticancer activity. In this study, we collected and analyzed over a thousand experimentally verified ACPs, specifically targeting peptides derived from natural sources. We developed a precise prediction model based on their sequence and structural features, and the model's evaluation results suggest its strong predictive ability for anticancer activity. To enhance reliability, we integrated the results of this model with those from other available methods. In total, we identified 176 potential ACPs, some of which were synthesized and further evaluated using the MTT colorimetric assay. All of these putative ACPs exhibited significant anticancer effects and selective cytotoxicity against specific tumor cells. In summary, we present a strategy for identifying and characterizing natural peptides with selective cytotoxicity against cancer cells, which could serve as novel therapeutic agents. Our prediction model can effectively screen new molecules for potential anticancer activity, and the results from in vitro experiments provide compelling evidence of the candidates' anticancer effects and selective cytotoxicity.

Indexed as

Antineoplastic AgentsComputer SimulationPeptidesBiological ProductsCell Line, TumorCell SurvivalDrug Screening Assays, AntitumorHumansMachine LearningNeoplasmsAntineoplastic AgentsBiological ProductsPeptidesanticancer activityanticancer peptideantitumor peptidein silico analysisin vitro experimentsmachine learningselective cytotoxicity

Identifiers

PMID38999958
PMCPMC11240926

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.