Evidence map›Paper›PMID 32612385›Full record

ArticleCancer management and research2020

miRNA-181a-5p Enhances the Sensitivity of Cells to Cisplatin in Esophageal Adenocarcinoma by Targeting CBLB.

Song Yang, Peng Wang, Songhua Wang, Aihua Cong, Qi Zhang, Wenhao Shen, Xiangyi Li, Wei Zhang, Gaohua Han

Open access · goldAbstract read
In one paragraph

Article in Cancer management and research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

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  5. Role of miR‑181a‑5p in cancer (Review).International journal of oncology · 2023
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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

9 authors at 2 institutions in 1 country.

Song Yang *Department of Oncology, Taizhou People's Hospital, Taizhou, Jiangsu 225300, People's Republic of China.
Peng Wang *Department of Oncology, Taizhou People's Hospital, Taizhou, Jiangsu 225300, People's Republic of China.
Songhua WangDepartment of Oncology, Taizhou People's Hospital, Taizhou, Jiangsu 225300, People's Republic of China.
Aihua CongDepartment of Oncology, Taizhou People's Hospital, Taizhou, Jiangsu 225300, People's Republic of China.
Qi ZhangDepartment of Oncology, Taizhou People's Hospital, Taizhou, Jiangsu 225300, People's Republic of China.
Wenhao ShenDepartment of Oncology, Taizhou People's Hospital, Taizhou, Jiangsu 225300, People's Republic of China.
Xiangyi LiDepartment of Endocrinology, Taizhou People's Hospital, Taizhou, Jiangsu 225300, People's Republic of China.
Wei ZhangDepartment of Infectious Diseases, Taizhou People's Hospital, Taizhou 225300, Jiangsu, People's Republic of China.
Gaohua HanDepartment of Oncology, Taizhou People's Hospital, Taizhou, Jiangsu 225300, People's Republic of China.
Taizhou People's Hospital · CNNantong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCisplatin (CDDP) is extensively used for esophageal adenocarcinoma (EAC) chemotherapy, while cisplatin resistance is getting worse. microRNA-181a-5p (miR-181a-5p) has been reported to play an important role in various human cancers. However, the effect and underlying mechanism of miR-181a-5p in cisplatin resistance of EAC remain unclear.

methodsCisplatin-resistant EAC cells OE19/CDDP and parental sensitive OE19 cells were applied for experiments in vitro. The expressions of miR-181a-5p and CBLB were measured by quantitative real-time polymerase chain reaction (qRT-PCR) or Western blot. The cisplatin resistance of cells was expressed by cell viability, IC50 and apoptosis rate by using CCK-8 assay or flow cytometry. The interaction between miR-181a-5p and CBLB was evaluated by luciferase reporter assay and RIP assay. In vivo experiments were conducted via the murine xenograft model.

resultsmiR-181a-5p was highly expressed while CBLB was lowly expressed in OE19 cell lines compared with OE19/CDDP cells. In cisplatin-resistant OE19/CDDP cells, miR-181a-5p up-regulation or CBLB knockdown inhibited cell viability and inducted apoptosis. In cisplatin-sensitive OE19 cells, miR-181a-5p inhibition or CBLB overexpression promoted cell viability and suppressed apoptosis. CBLB was confirmed to be a target of miR-181a-5p, and rescue assay showed CBLB overexpression reversed the suppression of OE19/CDDP cell viability induced by miR-181a-5p up-regulation, and its down-regulation attenuated miR-181a-5p-inhibition-mediated enhancement of OE19 cell viability. In addition, miR-181a-5p up-regulation enhanced the cytotoxicity of cisplatin in EAC in vivo.

conclusionmiR-181a-5p enhanced the sensitivity of cells to cisplatin in EAC by targeting CBLB, indicating a promising sensitizer of cisplatin therapy in clinical esophageal cancer.

Indexed as

CBLBcisplatin resistanceEACmiR-181a-5p

Identifiers

PMID32612385
PMCPMC7323973
OpenAlexW3037746870

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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.