Evidence map›Paper›PMID 32700738›Full record

ArticleBioscience reports2020

LncRNA HOTAIR contributes Taxol-resistance of hepatocellular carcinoma cells via activating AKT phosphorylation by down-regulating miR-34a.

Yunfei Duan, Jing Chen, Yu Yang, Zhen Qu, Yunjie Lu, Donglin Sun

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.4field-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, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
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  8. Article
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  12. Progress of HOTAIR-microRNA in hepatocellular carcinoma.Hereditary cancer in clinical practice · 2022
    Review
  13. Review
  14. Review
  15. Programmed cell death, redox imbalance, and cancer therapeutics.Apoptosis : an international journal on programmed cell death · 2021
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Yunfei DuanDepartment of Hepatopancreatobiliary Surgery, The Third Affiliated Hospital of Soochow University, Changzhou 213161, China.
Jing ChenDepartment of Hepatopancreatobiliary Surgery, The Third Affiliated Hospital of Soochow University, Changzhou 213161, China.
Yu YangDepartment of Hepatopancreatobiliary Surgery, The Third Affiliated Hospital of Soochow University, Changzhou 213161, China.
Zhen QuDepartment of Hepatopancreatobiliary Surgery, The Third Affiliated Hospital of Soochow University, Changzhou 213161, China.
Yunjie LuDepartment of Hepatopancreatobiliary Surgery, The Third Affiliated Hospital of Soochow University, Changzhou 213161, China.
Donglin SunDepartment of Hepatopancreatobiliary Surgery, The Third Affiliated Hospital of Soochow University, Changzhou 213161, China.
Soochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug resistance of Taxol leads to the treatment failure in hepatocellular carcinoma (HCC). LncRNA HOTAIR have drawn increasing attention in various diseases; its function and mechanism in Taxol-resistance in HCC remain unclear. In the present study, the two Taxol resistant HCC cell lines (HepG2/Taxol and SMMC7721/Taxol) were induced. The qRT-PCR data exhibited that over-expressed HOTAIR as well as low-expressed miR-34a were founded in HepG2/Taxol and SMMC7721/Taxol cells. HOTAIR knockdown suppresses proliferation, invasion and promotes apoptosis of in HepG2/Taxol and SMMC7721/Taxol cells through up-regulating miR-34a by MTT assay, transwell invasion assays and flow cytometry, while down-regulation of miR-34a had an opposite effect on reversing Taxol resistance. Cleaved caspase-3 and Bax were significantly up-regulated by si-HOTAIR transfection, while Bcl-2 level exhibited opposite trend. Besides, HOTAIR knockdown impaired Taxol-resistance in HCC by accommodating Akt phosphorylation and Wnt/β-catenin signaling via interacting with miR-34a. The present study may afford a valuable target for treating Taxol-resistance in HCC.

Indexed as

ApoptosisCarcinoma, HepatocellularCell MovementCell ProliferationDown-RegulationDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticGene Knockdown TechniquesHep G2 CellsHumansInhibitory Concentration 50Liver NeoplasmsMicroRNAsPaclitaxelPhosphorylationProto-Oncogene Proteins c-aktAKT1 protein, humanHOTAIR long untranslated RNA, humanMicroRNAsMIRN34 microRNA, humanPaclitaxelProto-Oncogene Proteins c-aktRNA, Long Noncodingapoptosishepatocellular carcinomaTaxol-resistance

Identifiers

PMID32700738
PMCPMC7396434
OpenAlexW3044051311

What OpenQuestion holds

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LicenceCC BY
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.