Evidence map›Paper›PMID 31162779›Full record

ArticleCancer science2019

Induced miR-31 by 5-fluorouracil exposure contributes to the resistance in colorectal tumors.

Yoshihito Nakagawa, Yuki Kuranaga, Tomomitsu Tahara, Hiromi Yamashita, Tomoyuki Shibata, Mitsuo Nagasaka, Kohei Funasaka, Naoki Ohmiya, Yukihiro Akao

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

15 citing papers in PubMed, 20 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

9 authors at 2 institutions in 1 country.

Yoshihito NakagawaDepartment of Gastroenterology, School of Medicine, Fujita Health University, Aichi, Japan.ORCID https://orcid.org/0000-0001-8689-492X
Yuki KuranagaThe United Graduate School of Drug Discovery and Medical Information Sciences, Gifu University, Gifu, Japan.
Tomomitsu TaharaDepartment of Gastroenterology, School of Medicine, Fujita Health University, Aichi, Japan.
Hiromi YamashitaDepartment of Gastroenterology, School of Medicine, Fujita Health University, Aichi, Japan.
Tomoyuki ShibataDepartment of Gastroenterology, School of Medicine, Fujita Health University, Aichi, Japan.
Mitsuo NagasakaDepartment of Gastroenterology, School of Medicine, Fujita Health University, Aichi, Japan.
Kohei FunasakaThe United Graduate School of Drug Discovery and Medical Information Sciences, Gifu University, Gifu, Japan.
Naoki OhmiyaDepartment of Gastroenterology, School of Medicine, Fujita Health University, Aichi, Japan.
Yukihiro AkaoThe United Graduate School of Drug Discovery and Medical Information Sciences, Gifu University, Gifu, Japan.ORCID https://orcid.org/0000-0001-8902-5367
Fujita Health University · JPGifu University · JP

Funding

Fujita Health University
6 · The paper itself

Abstract

Drug resistance makes treatment difficult in cancers. The present study identifies and analyzes drug resistance-related miRNA in colorectal cancer. We established 4 types of 5-fluorouracil (5-FU)-resistant colon cancer cell lines in vitro and in vivo. We then analyzed the miRNA expression profile by miRNA array in these 4 cell lines, and identified the drug resistance-related miRNAs. We examined the expression levels of the identified miRNA in 112 colorectal tumor samples from the patients. We identified 12 possible miRNAs involved in 5-FU resistance by miRNA arrays. We then examined the relationship between miR-31, which was the most promising among them, and drug resistance. The ectopic expression of mimic miR-31 showed significant 5-FU resistance in the parental DLD-1 cells, while anti-miR-31 caused significant growth inhibition in DLD/F cells; that is, 5-FU-resistant colon cancer cell line DLD-1 under exposure to 5-FU. When we exposed high doses of 5-FU to parent or 5-FU-resistant cells, the expression levels of miR-31 were raised higher than those of controls. Notably, the expression levels of miR-31 were positively correlated with the grade of clinical stages of colorectal tumors. The protein expression levels of factors inhibiting hypoxia-inducible factor 1 were downregulated by transfection of mimic miR-31 into DLD-1 cells. This study provides evidence supporting the association of miR-31 with 5-FU drug resistance and clinical stages of colorectal tumors.

Indexed as

Antimetabolites, AntineoplasticCell Line, TumorColorectal NeoplasmsDown-RegulationDrug Resistance, NeoplasmFluorouracilGene Expression Regulation, NeoplasticHumansMicroRNAsTransfectionAntimetabolites, AntineoplasticFluorouracilMicroRNAsMIRN31 microRNA, human5-fluorouracilcolorectal cancerdrug resistancemicroRNAWarburg effect

Identifiers

PMID31162779
PMCPMC6676105
OpenAlexW2948143078

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.