Evidence map›Paper›PMID 37247274›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2023

LncRNA CASC2 Inhibits Progression of Glioblastoma by Regulating the Expression of AKT in T98G Cell Line, Treated by TMZ and Thiosemicarbazone Complex.

Shohreh Shahmir, Neda Zahmatkesh, Sina Mirzaahmadi, Golnaz Asaadi Tehrani

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
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  3. Roles of TRPM channels in glioma.Cancer biology & therapy · 2024
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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

4 authors at 1 institution in 1 country.

Shohreh ShahmirDepartment of Genetics, Zanjan Branch, Islamic Azad University, Zanjan, Iran.
Neda ZahmatkeshDepartment of Genetics, Zanjan Branch, Islamic Azad University, Zanjan, Iran.
Sina MirzaahmadiDepartment of Genetics, Zanjan Branch, Islamic Azad University, Zanjan, Iran.
Golnaz Asaadi TehraniDepartment of Genetics, Zanjan Branch, Islamic Azad University, Zanjan, Iran.
Islamic Azad University of Zanjan · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim of this study was to evaluate the expression alterations of CACS2 and its target gene, AKT, in T98G cell line treated with Temozolomide and Thiosemicarbazone complex (Ni, Cu) and to compare the results with each other.

methodsTemozolomide and Thiosemicarbazone complexes were prepared in different concentrations. Cell culturing of T98G cell line was carried out and was classified into 3 groups based on the incubation time (24, 48, and 72h) with utilized agents, after RNA extraction the expression level of CACS2 and AKT genes were evaluated by Real-time PCR. Ultimately, the results were analyzed by Rest software.

resultsCASC2 expression under Temozolomide treatment at different concentrations (100, 150, 200, and 250 µM) and different time periods (24, 48, and 72h) was increased. Moreover, its expression was significantly upregulated after treating with Ni at the concentrations of 100.5 and 104 µM after 24h. Furthermore, its expression was augmented after 72 h Cu treatment at the concentrations of 15, 16, 17, and 18 µM. In addition, AKT expression after Temozolomide and Thiosemicarbazone complex treatment was significantly decreased (P <0.001). The results showed that the expression alterations of CASC2 and its target gene, AKT, after treatment with Temozolomide and Thiosemicarbazone are highly depended on incubation time and concentration.

conclusionIn a conclusion, the studied agents at different concentrations and times showed a high potential to control the expression of the studied lncRNA and gene in glioblastoma cells.

Indexed as

Brain NeoplasmsGlioblastomaRNA, Long NoncodingAntineoplastic Agents, AlkylatingCell Line, TumorDrug Resistance, NeoplasmHumansProto-Oncogene Proteins c-aktTemozolomideAntineoplastic Agents, AlkylatingProto-Oncogene Proteins c-aktRNA, Long NoncodingTemozolomideGlioblastomaTemozolomideThiosemicarbazone

Identifiers

PMID37247274
PMCPMC10495874
OpenAlexW4378714269

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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.