Evidence map›Paper›PMID 30997746›Full record

ArticleJournal of cellular and molecular medicine2019

LncRNA KCNQ1OT1 enhanced the methotrexate resistance of colorectal cancer cells by regulating miR-760/PPP1R1B via the cAMP signalling pathway.

Di Xian, Yu Zhao

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
4.1field-weighted citation impact, top 4% 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

47 citing papers in PubMed, 67 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. LncRNATranslational cancer research · 2024
    Article
  9. Review
  10. New long noncoding RNA biomarkers and ceRNA networks on miR-616-3p in colorectal cancer: Bioinformatics-based study.Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2024
    Article
  11. Article
  12. The Expression ofJournal of immunology research · 2023
    Article
  13. Article
  14. Role of Non-Coding RNAs in Colorectal Cancer: Focus on Long Non-Coding RNAs.International journal of molecular sciences · 2022
    Review
  15. Article
  16. Article
  17. Long Non-Coding RNAInternational journal of molecular sciences · 2022
    Article
  18. Article
  19. Review
  20. Article
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

2 authors at 1 institution in 1 country.

Di XianDepartment of Emergency Surgery, Sichuan Academy of Medical Sciences & Sichaun Provincial People's Hospital, Chengdu, Sichuan, China.
Yu ZhaoDepartment of Emergency Surgery, Sichuan Academy of Medical Sciences & Sichaun Provincial People's Hospital, Chengdu, Sichuan, China.ORCID 0000-0002-0982-5944
Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to explore the mechanism of the KCNQ1OT1/miR-760/PPP1R1B axis acting to regulate methotrexate (MTX) resistance of colorectal cancer (CRC). Differentially expressed mRNAs and lncRNAs in MTX-sensitive CRC cell lines and MTX-resistant cell lines were determined through microarray analysis. Application of bioinformatics analysis was aimed to uncover the relationships among the lncRNAs/miRNAs/mRNAs, and to demonstrate the effects of cAMP signalling pathway in MTX-resistant CRC. The expression level of RNA and proteins was, respectively, detected using qRT-PCR and Western blot assays, whereas the dual-luciferase reporter gene assay was implemented to verify the targeted relationship. The influence of the lncRNA/miRNA/mRNA axis on biological functions of MTX-resistant cells and on the growth of tumours determined through both vitro and vivo experiments. LncRNA KCNQ1OT1 and PPP1R1B mRNA were overexpressed in MTX-resistant CRC tumour cells. KCNQ1OT1 functioned as a sponge of miR-760, which targeted PPP1R1B. Knockdown of KCNQ1OT1 enhanced chemosensitivity towards MTX through the sponging of miR-760. MiR-760 expressed at low levels targeted PPP1R1B in the activated cAMP signalling pathway under MTX treatment. Knockdown of KCNQ1OT1 dampened the proliferation of MTX-resistant (HT29/MTX) cells by regulating the miR-760/PPP1R1B axis, which also induced cell cycle arrest together with apoptosis. KCNQ1OT1 regulated the expression of PPP1R1B and the downstream genes CREB and CBP in the cAMP signalling pathway. MTX showed a suppressive function on CRC progression. KCNQ1OT1 enhanced the MTX resistance of CRC cells by regulating miR-760-mediated PPP1R1B expression via the cAMP signalling pathway.

Indexed as

AnimalsAntimetabolites, AntineoplasticApoptosisCaco-2 CellsCell Cycle CheckpointsCell ProliferationColorectal NeoplasmsCREB-Binding ProteinCyclic AMPCyclic AMP Response Element-Binding ProteinDopamine and cAMP-Regulated Phosphoprotein 32Drug Resistance, NeoplasmGene Regulatory NetworksHT29 CellsHumansMethotrexateAntimetabolites, AntineoplasticCREB1 protein, humanCREB-Binding ProteinCyclic AMPCyclic AMP Response Element-Binding ProteinDopamine and cAMP-Regulated Phosphoprotein 32KCNQ1OT1 RNAMethotrexateMicroRNAsMIRN760 microRNA, humanPPP1R1B protein, humanRNA, Long Noncodingbioinformatics analysiscAMP signalling pathwaycolorectal cancerlncRNAmethotrexate

Identifiers

PMID30997746
PMCPMC6533496
OpenAlexW2937130869

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.