Evidence map›Paper›PMID 31173223›Full record

ArticleMolecular medicine reports2019

Long non‑coding RNA CASC2 enhances berberine‑induced cytotoxicity in colorectal cancer cells by silencing BCL2.

Wei Dai, Liyuan Mu, Yali Cui, Yingying Li, Ping Chen, Hongjian Xie, Xia Wang

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 32 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Wei DaiDepartment of Medical Laboratory, West China Second University Hospital, Sichuan University, Chengdu, Sichuan 610000, P.R. China.
Liyuan MuDepartment of Medical Laboratory, West China Second University Hospital, Sichuan University, Chengdu, Sichuan 610000, P.R. China.
Yali CuiDepartment of Medical Laboratory, West China Second University Hospital, Sichuan University, Chengdu, Sichuan 610000, P.R. China.
Yingying LiDepartment of Medical Laboratory, West China Second University Hospital, Sichuan University, Chengdu, Sichuan 610000, P.R. China.
Ping ChenDepartment of Medical Laboratory, West China Second University Hospital, Sichuan University, Chengdu, Sichuan 610000, P.R. China.
Hongjian XieDepartment of Medical Laboratory, West China Second University Hospital, Sichuan University, Chengdu, Sichuan 610000, P.R. China.
Xia WangDepartment of Medical Laboratory, West China Second University Hospital, Sichuan University, Chengdu, Sichuan 610000, P.R. China.
Sichuan University · CNWest China Second University Hospital of Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Berberine, a natural isoquinoline alkaloid derived from Berberis species, has been reported to have anticancer effects. However, the mechanisms of action in human colorectal cancer (CRC) are not well established to date. In the present study, the cell cytotoxicity effect of berberine on human CRC cells, as well as the possible mechanisms involved, was investigated. The results of the cell viability and apoptosis assay revealed that treatment of CRC cells with berberine resulted in inhibition of cell viability and activation of cell apoptosis in a concentration‑dependent manner. To reveal the underlying mechanism of berberine‑induced anti‑tumor activity and cell apoptosis, RNA‑sequencing followed by reverse‑transcription quantitative PCR were performed. In addition, RNA immunoprecipitation, chromatin immunoprecipitation and western blot analysis were used to identify the functional regulation of CASC2/EZH2/BCL2 axis in berberine‑induced CRC cell apoptosis. The data revealed that lncRNA CASC2 was upregulated by berberine treatment. Gain‑ or loss‑of‑function assays suggested that lncRNA CASC2 was required for the berberine‑induced inhibition of cell viability and activation of cell apoptosis. Subsequently, the downstream antiapoptotic gene BCL2 was identified as a functional target of the berberine/CASC2 mechanism, as BCL2 reversed the berberine/CASC2‑induced cell cytotoxicity. lncRNA CASC2 silenced BCL2 expression by binding to the promoter region of BCL2 in an EZH2‑dependent manner. In summary, berberine may be a novel therapeutic agent for CRC and lncRNA CASC2 may serve as an important therapeutic target to improve the anticancer effect of berberine.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedAntineoplastic Agents, PhytogenicApoptosisBerberineCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsEnhancer of Zeste Homolog 2 ProteinFemaleHCT116 CellsHT29 CellsHumansMaleAntineoplastic Agents, PhytogenicBCL2 protein, humanBerberineEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanlong non-coding RNA CASC2, humanProto-Oncogene Proteins c-bcl-2RNA, Long NoncodingRNA, Small InterferingTumor Suppressor Proteins

Identifiers

PMID31173223
PMCPMC6625213
OpenAlexW2948222148

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.