Evidence map›Paper›PMID 38665777›Full record

ArticleTurkish journal of biology = Turk biyoloji dergisi2024

Prognostic gene biomarkers for c-Src inhibitor Si162 sensitivity in melanoma cells.

Seyhan Türk, Ayşegül Yilmaz, Ümit Yavuz Malkan, Gülberk Uçar, Can Türk

Open access · diamondAbstract read
In one paragraph

Article in Turkish journal of biology = Turk biyoloji dergisi, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

5 authors at 3 institutions in 2 countries.

Seyhan TürkDepartment of Biochemistry, Faculty of Pharmacy, Hacettepe University, Ankara, Turkiye.ORCID https://orcid.org/0000-0003-3843-4173
Ayşegül YilmazDepartment of Medical Microbiology, Faculty of Medicine, Lokman Hekim University, Ankara, Turkiye.ORCID https://orcid.org/0000-0002-9541-9853
Ümit Yavuz MalkanDepartment of Hematology, Faculty of Medicine, Hacettepe University, Ankara, Turkiye.ORCID https://orcid.org/0000-0001-5444-4895
Gülberk UçarDepartment of Biochemistry, Faculty of Pharmacy, Hacettepe University, Ankara, Turkiye.ORCID https://orcid.org/0000-0002-8647-1545
Can TürkDepartment of Medical Microbiology, Faculty of Medicine, Lokman Hekim University, Ankara, Turkiye.ORCID https://orcid.org/0000-0003-1514-7294
Hacettepe University · TRLaboratoire de Biochimie · FRLokman Hekim Üniversitesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/aim: Early detection and treatment are crucial in combating malignant melanoma. Src is an important therapeutic target in melanoma due to its association with cancer progression. However, developing effective Src-targeting drugs remains challenging and personalized medicine relies on biomarkers and targeted therapies for precise and effective treatment. This study focuses on Si162, a newly synthesized c-Src inhibitor, to identify reliable biomarkers for predicting Si162 sensitivity and explore associated biological characteristics and pathways in melanoma cells. Materials and methods: Primary melanoma cells (M1, M21, M24, M84, M133, M307, and M2025) were obtained from patients diagnosed with melanoma. Si162 cytotoxicity tests were performed using luminescent adenosine triphosphate detection and the half-maximal inhibitory concentration (IC Results: The cells revealed significant differences in response to Si162 based on the IC Conclusion: These findings contribute to our understanding of the underlying biological differences among melanoma cells and suggest potential biomarkers and pathways associated with Si162 response and resistance.

Indexed as

chemotherapyc-Src inhibitorgene biomarkerMelanomasi162

Identifiers

PMID38665777
PMCPMC11042866
OpenAlexW4392364632

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.