Evidence map›Paper›PMID 35117623›Full record

ArticleTranslational cancer research2020

Interaction between linc01615 and miR-491-5p regulates the survival and metastasis of colorectal cancer cells.

You Xiao, Fan Hu, Mei Li, Li Mo, Chongsi Xu, Xiaoyan Wang, Jing Nie, Lixia Yang, Biao Xie

Open access · diamondAbstract read
In one paragraph

Article in Translational cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
0.6field-weighted citation impact, top 42% 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

24 citing papers in PubMed, 26 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.

You XiaoDepartment One of Anorectal Surgery, The Second Affiliated Hospital of Hunan University of Chinese Medicine, Changsha 410005, China.
Fan HuDepartment One of Anorectal Surgery, The Second Affiliated Hospital of Hunan University of Chinese Medicine, Changsha 410005, China.
Mei LiDepartment One of Anorectal Surgery, The Second Affiliated Hospital of Hunan University of Chinese Medicine, Changsha 410005, China.
Li MoDepartment One of Anorectal Surgery, The Second Affiliated Hospital of Hunan University of Chinese Medicine, Changsha 410005, China.
Chongsi XuDepartment One of Anorectal Surgery, The Second Affiliated Hospital of Hunan University of Chinese Medicine, Changsha 410005, China.
Xiaoyan WangDepartment One of Anorectal Surgery, The Second Affiliated Hospital of Hunan University of Chinese Medicine, Changsha 410005, China.
Jing NieHunan Slack King Laboratory Animal Co., Ltd., Changsha 410125. China.
Lixia YangDepartment of Cancer, The First Affiliated Hospital of Changsha Medical School, Changsha 410219, China.
Biao XieDepartment One of Anorectal Surgery, The Second Affiliated Hospital of Hunan University of Chinese Medicine, Changsha 410005, China.
Second Affiliated Hospital of Hunan University of Traditional Chinese Medicine · CNThe First Hospital of Changsha · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe 5-year survival of colorectal cancer (CRC) has had no obvious improvement during the past decades, although a significant progress in treatments has been established. The molecular mechanisms that drive the progression of CRC are still unclear. This study aims to determine the biological activities of linc01615 and its regulatory microRNAs in CRC cells.

methodsThe expression of linc016150 and miR-491-5p was measured in six CRC cell lines and one normal colon mucosal epithelial cell line. Their effects on cell proliferation, apoptosis, invasion, and migration were tested in Caco-2 cells.

resultsLinc01615 mRNA expression was upregulated in six colorectal cancer cell lines compared to the normal colon mucosal epithelial cell line, which was negatively regulated by miR-491-5p in Caco-2 cells. Silencing of linc01615 gene expression significantly decreased cell proliferation, increased apoptosis, and inhibited invasion and migration in Caco-2 cells. Overexpression of linc01615 exhibited an opposite effect on silencing of linc01615 expression. Transfection with miR-491-5p mimics downregulated linc01615 expression and inhibited the biological activities of linc01615. In contrast, the inhibitor of miR-491-5p up-regulated linc01615 expression and subsequently enhanced the biological activities of linco1615. Also, overexpression of linc01615 can block the effects of miR-491-5p mimics in Caco-2 cells.

conclusionsLinc01615 functions as an oncogene while miR-491-5p functions as a tumor suppressor in colorectal cancer cells through negatively regulating each other; both are involved in cell proliferation, apoptosis, invasion, and migration in colorectal cancer cells.

Indexed as

apoptosisColorectal cancer (CRC)invasionlinc01615miR-491-5p

Identifiers

PMID35117623
PMCPMC8798974
OpenAlexW3011402595

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.