Evidence map›Paper›PMID 31268161›Full record

ArticleInternational journal of oncology2019

miR‑1 reverses multidrug resistance in gastric cancer cells via downregulation of sorcin through promoting the accumulation of intracellular drugs and apoptosis of cells.

Lang-Mei Deng, Tan Tan, Tian-Yi Zhang, Xue-Fei Xiao, Huan Gu

Open access · hybridAbstract read
In one paragraph

Article in International journal of oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

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  8. MicroRNA-1: Diverse role of a small player in multiple cancers.Seminars in cell & developmental biology · 2022
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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

5 authors at 3 institutions in 1 country.

Lang-Mei DengCritical Care Center, The Third Xiangya Hospital of Central South University, Changsha, Hunan 410013, P.R. China.
Tan TanDepartment of Inspection, Chenzhou No.1 People's Hospital, Chenzhou, Hunan 423000, P.R. China.
Tian-Yi ZhangCritical Care Center, The Third Xiangya Hospital of Central South University, Changsha, Hunan 410013, P.R. China.
Xue-Fei XiaoCritical Care Center, The Third Xiangya Hospital of Central South University, Changsha, Hunan 410013, P.R. China.
Huan GuDepartment of Gastroenterology, Xiangya Hospital of Central South University, Changsha, Hunan 410008, P.R. China.
Central South University · CNChenzhou First People's Hospital · CNXiangya Hospital Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric cancer (GC) is one of the most common cancers worldwide and results in the second greatest rate of cancer‑associated mortality globally. Multidrug resistance (MDR) often develops during the chemotherapy, resulting in the failure of treatment. To investigate the molecular mechanism of MDR, the roles of microRNA (miR)‑1 were studied in GC. Reverse transcription‑quantitative polymerase chain reaction and western blotting were used to investigate the expression levels of miR‑1 and sorcin in SGC7901/ADM and SGC7901/VCR cell lines. The effect of miR‑1 on the half maximal inhibitory concentration (IC50), cell apoptosis rates and drug accumulation was uncovered by MTT assay and flow cytometric analysis. Furthermore, dual‑luciferase assay and western blotting were used to determine the target of miR‑1 in GC. It was demonstrated that miR‑1 was highly downregulated in MDR GC cell lines, including SGC7901/ADM and SGC7901/VCR. Overexpression of miR‑1 in MDR GC cells decreased IC50, but increased the cell apoptosis rates and promoted the drug accumulation in cancer cells. Dual‑luciferase activity assay indicated that sorcin was the target of miR‑1 in GC. In addition, overexpression of sorcin could partially reverse the effect of miR‑1 in MDR GC cells. The role of miR‑1 in MDR GC cells makes it a potential therapeutic target for a successful clinical outcome.

Indexed as

Antibiotics, AntineoplasticAntineoplastic Agents, PhytogenicApoptosisCalcium-Binding ProteinsCell ProliferationDoxorubicinDrug Resistance, MultipleDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHumansMicroRNAsStomach NeoplasmsTumor Cells, CulturedVincristineAntibiotics, AntineoplasticAntineoplastic Agents, PhytogenicCalcium-Binding ProteinsDoxorubicinMicroRNAsMIRN1 microRNA, humanSRI protein, humanVincristine

Identifiers

PMID31268161
PMCPMC6615921
OpenAlexW2955510822

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.