Evidence map›Paper›PMID 24649007›Full record

ArticleBiomedical reports2013

Construction and identification of the pshRNA-CACNA1G-SH-SY5Ycells targeted to silence Cav3.1 mRNA expression.

Xianjie Wen, Shiyuan Xu, Hongzhen Liu, Hua Liang, Chenxiang Yang, Hanbing Wang

Open access · bronzeAbstract read
In one paragraph

Article in Biomedical reports, 2013. 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
0.1field-weighted citation impact, top 44% 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

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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, 2 citations in OpenAlex.

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

6 authors at 3 institutions in 1 country.

Xianjie WenDepartment of Anesthesiology, Zhujiang Hospital of Southern Medical University, Guangzhou, Guangdong 510282, P.R. China ; Department of Anesthesiology, The First People's Hospital of Foshan and Foshan Hospital of Sun Yat-Sen University, Foshan, Guangdong 528000, P.R. China.
Shiyuan XuDepartment of Anesthesiology, Zhujiang Hospital of Southern Medical University, Guangzhou, Guangdong 510282, P.R. China.
Hongzhen LiuDepartment of Anesthesiology, The First People's Hospital of Foshan and Foshan Hospital of Sun Yat-Sen University, Foshan, Guangdong 528000, P.R. China.
Hua LiangDepartment of Anesthesiology, The First People's Hospital of Foshan and Foshan Hospital of Sun Yat-Sen University, Foshan, Guangdong 528000, P.R. China.
Chenxiang YangDepartment of Anesthesiology, The First People's Hospital of Foshan and Foshan Hospital of Sun Yat-Sen University, Foshan, Guangdong 528000, P.R. China.
Hanbing WangDepartment of Anesthesiology, The First People's Hospital of Foshan and Foshan Hospital of Sun Yat-Sen University, Foshan, Guangdong 528000, P.R. China.
First People's Hospital of Foshan · CNSouthern Medical University · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-type calcium channels are a class of low voltage-dependent calcium channels that may be activated following minor depolarizations of the cell membrane. Cav3.1 is the dominant subtype of the T-type calcium channel in SH-SY5Y cells. T-type channels play a key role in the regulation of the intracellular calcium concentration, which is involved in the neurotoxic effect of local anesthetics. However, there is a lack of specific inhibitors of T-type calcium channels. The existing T-type calcium channel inhibitors exhibit poor specificity and may block the high voltage-dependent calcium channels, such as the L- and N-type channels. Furthermore, there is no selectivity to the subtype of the T-type calcium channel. Therefore, the development of a specific T-type calcium channel inhibitor may contribute to the elucidation of the functions and characteristics of T-type calcium channels. The aim of this study was to silence the Cav3.1 mRNA expression in SH-SY5Y cells via the RNA interference (RNAi) method in order to construct pshRNA-CACNA1G-SH-SY5Y cells and assess Cav3.1 mRNA and protein expression by western blot analysis and reverse transcription-polymerase chain reaction (RT-PCR) to identify the constructed cell line. The results demonstrated that Cav3.1 mRNA and protein expression were significantly reduced following transfection with the SH-SY5Y cells by the supernatant liquors. The results also demonstrated that the pshRNA-CACNA1G-SH-SY5Y cells were successfully constructed. These findings may contribute to the elucidation of the functions of Cav3.1 in SH-SY5Y cells.

Indexed as

Cav3.1reverse transcription-polymerase chain reactionRNA interferenceT-type calcium channelwestern blot analysis

Identifiers

PMID24649007
PMCPMC3917022
OpenAlexW2030625394

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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.