Evidence map›Paper›PMID 33588834›Full record

ArticleCancer cell international2021

LncRNA LINC00342 contributes to the growth and metastasis of colorectal cancer via targeting miR-19a-3p/NPEPL1 axis.

Peng Shen, Lili Qu, Jingjing Wang, Quchen Ding, Chuanwen Zhou, Rui Xie, Honggang Wang, Guozhong Ji

Abstract read
In one paragraph

Article in Cancer cell international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

  1. Article
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  9. [LncRNA LINC00342 regulates gastric cancer cell proliferation, migration and invasion by targeting miR-596].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2023
    Article
  10. Article
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  12. The Role of Long Noncoding RNA (lncRNAs) Biomarkers in Renal Cell Carcinoma.International journal of molecular sciences · 2022
    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

8 authors.

Peng ShenThe Second Affiliated Hospital of Nanjing Medical University, Nanjing, 210000, China.
Lili QuThe Second Affiliated Hospital of Nanjing Medical University, Nanjing, 210000, China.
Jingjing WangThe Second Affiliated Hospital of Nanjing Medical University, Nanjing, 210000, China.
Quchen DingThe Second Affiliated Hospital of Nanjing Medical University, Nanjing, 210000, China.
Chuanwen ZhouThe Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, Huai'an, 223300, China.
Rui XieThe Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, Huai'an, 223300, China.
Honggang WangThe Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, Huai'an, 223300, China.
Guozhong JiThe Second Affiliated Hospital of Nanjing Medical University, Nanjing, 210000, China. jgz@njmu.edu.cn.ORCID http://orcid.org/0000-0003-4968-8267

Funding

The Science and Technology Development Foundation of Nanjing Medical University of China 2016NJMUZD03
6 · The paper itself

Abstract

backgroundLong intergenic non-protein coding RNA 00342 (LINC00342) has been identified as a novel oncogene. However, the functional role of LINC00342 in colorectal cancer (CRC) remains unclear.

methodsThe expression of LINC00342 is detected by real-time PCR (RT-PCR) analysis. Cell proliferation, migration and invasion and xenograft model are examined to analyze the biological functions of LINC00342 in vitro and in vivo using colony formation, would healing and transwell analyses. Dual-luciferase reporter and RNA immunoprecipitation (RIP) assays are used to identify the target interactions between LINC00342, miR-19a-3p and aminopeptidase like 1 (NPEPL1).

resultsLINC00342 was highly expressed in CRC. Down-regulation of LINC00342 inhibited cell proliferation and metastasis of CRC cells. Moreover, knocking down LINC00342 inhibited the tumor growth in vivo. Mechanistic investigation revealed that LINC00342 might sponge miR-19a-3p to regulate NPEPL1 expression. Further investigation indicated that the ontogenesis facilitated by LINC00342 was inhibited due to the depletion of NPEPL1.

conclusionLINC00342 promotes CRC progression by competitively binding miR-19a-3p with NPEPL1.

Indexed as

Colorectal cancerInvasionLINC00342miR-19a-3pNPEPL1Proliferation

Identifiers

PMID33588834
PMCPMC7885559

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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.