Evidence map›Paper›PMID 32652877›Full record

ArticleJournal of cellular and molecular medicine2020

LINC00160 mediated paclitaxel-And doxorubicin-resistance in breast cancer cells by regulating TFF3 via transcription factor C/EBPβ.

Huaiguo Wu, Juan Gu, Daoping Zhou, Wei Cheng, Yueping Wang, Qingping Wang, Xuedong Wang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.7field-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

25 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  6. Review
  7. Breast Cancer Chemoresistance: Insights into the Regulatory Role of lncRNA.International journal of molecular sciences · 2023
    Review
  8. Long Noncoding RNAs in Taxane Resistance of Breast Cancer.International journal of molecular sciences · 2023
    Review
  9. Landscape of NcRNAs involved in drug resistance of breast cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
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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 3 institutions in 2 countries.

Huaiguo WuCenter for Precision Medicine, Anhui No.2 Provincial People's Hospital, Hefei, China.
Juan GuDepartment of Medical Laboratory Science, The Fifth People's Hospital of Wuxi, Nanjing Medical University, Wuxi, China.
Daoping ZhouCenter for Precision Medicine, Anhui No.2 Provincial People's Hospital, Hefei, China.
Wei ChengCenter for Precision Medicine, Anhui No.2 Provincial People's Hospital, Hefei, China.
Yueping WangCenter for Precision Medicine, Anhui No.2 Provincial People's Hospital, Hefei, China.
Qingping WangCenter for Precision Medicine, Anhui No.2 Provincial People's Hospital, Hefei, China.
Xuedong WangCenter for Precision Medicine, Anhui No.2 Provincial People's Hospital, Hefei, China.ORCID 0000-0003-3430-1082
Anhui Provincial Hospital · CNJiangnan University · CNUniversity of Massachusetts Boston · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemoresistance represents a major challenge in breast cancer (BC) treatment. This study aimed to probe the roles of LINC00160 in paclitaxel- and doxorubicin-resistant BC cells. Three pairs of BC and adjacent normal tissue were used for lncRNA microarray analysis. Paclitaxel-resistant MCF-7 (MCF-7/Tax) and doxorubicin-resistant BT474 (BT474/Dox) cells were generated by exposure of parental drug-sensitive MCF-7 or BT474 cells to gradient concentrations of drugs. Correlation between LINC00160 expression and clinical response to paclitaxel in BC patients was examined. Short interfering RNAs specifically targeting LINC00160 or TFF3 were designed to construct LINC00160- and TFF3-depleted BC cells to discuss their effects on biological episodes of MCF-7/Tax and BT474/Dox cells. Interactions among LINC00160, transcription factor C/EBPβ and TFF3 were identified. MCF-7/Tax and BT474/Dox cells stable silencing of LINC00160 were transplanted into nude mice. Consequently, up-regulated LINC00160 led to poor clinical response to paclitaxel in BC patients. LINC00160 knockdown reduced drug resistance in MCF-7/Tax and BT474/Dox cells and reduced cell migration and invasion. LINC00160 recruited C/EBPβ into the promoter region of TFF3 and increased TFF3 expression. LINC00160-depleted MCF-7/Tax and BT474/Dox cells showed decreased tumour growth rates in nude mice. Overall, we identified a novel mechanism of LINC00160-mediated chemoresistance via the C/EBPβ/TFF3 axis, highlighting the potential of LINC00160 for treating BC with chemoresistance.

Indexed as

Gene Expression Regulation, NeoplasticRNA, Long NoncodingAdultAnimalsBiomarkers, TumorBreast NeoplasmsCCAAT-Enhancer-Binding Protein-betaCell Line, TumorDisease Models, AnimalDoxorubicinDrug Resistance, NeoplasmFemaleHumansMCF-7 CellsMiceMiddle AgedBiomarkers, TumorCCAAT-Enhancer-Binding Protein-betaCEBPB protein, humanDoxorubicinPaclitaxelRNA, Long NoncodingTFF3 protein, humanTranscription FactorsTrefoil Factor-3breast cancerC/EBPβdrug resistancelong non-coding RNA-00160TFF3

Identifiers

PMID32652877
PMCPMC7412707
OpenAlexW3042093479

What OpenQuestion holds

Textmetadata
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.