Evidence map›Paper›PMID 29267503›Full record

ArticleBrazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica2017

Long non-coding RNA LINC00261 sensitizes human colon cancer cells to cisplatin therapy.

Z K Wang, L Yang, L L Wu, H Mao, Y H Zhou, P F Zhang, G H Dai

Open access · goldAbstract read
In one paragraph

Article in Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.8field-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

39 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
  2. Clinical Significance ofDiseases (Basel, Switzerland) · 2025
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  17. Low miR-1273a expression predicts poor prognosis of colon cancer and facilitates tumor cell proliferation, migration, and invasion.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2021
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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 1 institution in 1 country.

Z K WangThe Second Department of Medical Oncology, Chinese People's Liberation Army General Hospital, Beijing, China.
L YangThe Second Department of Medical Oncology, Chinese People's Liberation Army General Hospital, Beijing, China.
L L WuTumor Center Laboratory, Chinese People's Liberation Army General Hospital, Beijing, China.
H MaoThe Second Department of Medical Oncology, Chinese People's Liberation Army General Hospital, Beijing, China.
Y H ZhouThe Second Department of Medical Oncology, Chinese People's Liberation Army General Hospital, Beijing, China.
P F ZhangThe Second Department of Medical Oncology, Chinese People's Liberation Army General Hospital, Beijing, China.
G H DaiThe Second Department of Medical Oncology, Chinese People's Liberation Army General Hospital, Beijing, China.
Chinese People's Liberation Army · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colon cancer is one of the most common digestive tumors. The present study aimed to explore the functional role, as well as the underlying mechanism of long non-coding RNA LINC00261 in colon cancer. Expression of LINC00261 was analyzed in colon cancer cell lines and human normal cell lines. Acquired resistance cell lines were then built and the acquired resistance efficiency was detected by evaluating cell viability. Thereafter, the effects of LINC00261 overexpression on cisplatin-resistant colon cancer cells were measured, as well as cell apoptosis, viability, migration, and invasion. Subsequently, we investigated the interaction of LINC00261 and β-catenin. The results showed that the LINC00261 gene was down-regulated in colon cancer cell lines and tissues, and in cisplatin-resistant cells. LINC00261 overexpression might relieve cisplatin resistance of colon cancer cells via promoting cell apoptosis, and inhibiting cell viability, migration, and invasion. Moreover, LINC00261 might down-regulate nuclear β-catenin through restraining β-catenin from cytoplasm into nuclei or it could also promote β-catenin degradation and inhibit activation of Wnt pathway. Finally, LINC00261 reduced cisplatin resistance of colon cancer in vivo and enhanced the anti-colon cancer effect of cisplatin through reducing tumor volume and weight.

Indexed as

Analysis of VarianceAntineoplastic AgentsApoptosisApoptosis Regulatory Proteinsbeta CateninBlotting, WesternCell Migration AssaysCell ProliferationCisplatinColonic NeoplasmsDown-RegulationGene Expression Regulation, NeoplasticHCT116 CellsHT29 CellsHumansReproducibility of ResultsAntineoplastic AgentsApoptosis Regulatory Proteinsbeta CateninCisplatinlong non-coding RNA 00261, humanRNA, Long NoncodingTetrazolium SaltsThiazolesthiazolyl blue

Identifiers

PMID29267503
PMCPMC5731330
OpenAlexW2774339488

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.