Evidence map›Paper›PMID 35310912›Full record

ArticleJournal of oncology2022

LncSNHG1 Promoted CRC Proliferation through the miR-181b-5p/SMAD2 Axis.

Qi Huang, Zhi Yang, Jin-Hai Tian, Pei-Dong You, Jia Wang, Rong Ma, Jingjing Yu, Xu Zhang, Jia Cao, Jie Cao and 1 more

Abstract read
In one paragraph

Article in Journal of oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
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

11 authors.

Qi HuangThe Biochip Research Center of General Hospital of Ningxia Medical University, Yinchuan 750004, China.ORCID https://orcid.org/0000-0002-3135-1140
Zhi YangGuangzhou First People's Hospital, Guangzhou 510180, China.ORCID https://orcid.org/0000-0003-1958-482X
Jin-Hai TianThe Biochip Research Center of General Hospital of Ningxia Medical University, Yinchuan 750004, China.ORCID https://orcid.org/0000-0002-4823-9323
Pei-Dong YouThe Biochip Research Center of General Hospital of Ningxia Medical University, Yinchuan 750004, China.ORCID https://orcid.org/0000-0001-9521-5415
Jia WangThe Biochip Research Center of General Hospital of Ningxia Medical University, Yinchuan 750004, China.ORCID https://orcid.org/0000-0001-9800-4277
Rong MaThe Biochip Research Center of General Hospital of Ningxia Medical University, Yinchuan 750004, China.ORCID https://orcid.org/0000-0001-8211-7656
Jingjing YuThe Biochip Research Center of General Hospital of Ningxia Medical University, Yinchuan 750004, China.ORCID https://orcid.org/0000-0003-3196-8738
Xu ZhangThe Biochip Research Center of General Hospital of Ningxia Medical University, Yinchuan 750004, China.ORCID https://orcid.org/0000-0002-6132-8611
Jia CaoThe Biochip Research Center of General Hospital of Ningxia Medical University, Yinchuan 750004, China.ORCID https://orcid.org/0000-0002-3541-0689
Jie CaoGuangzhou First People's Hospital, Guangzhou 510180, China.ORCID https://orcid.org/0000-0002-0401-590X
Li-Bin WangThe Biochip Research Center of General Hospital of Ningxia Medical University, Yinchuan 750004, China.ORCID https://orcid.org/0000-0002-7861-1560

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To investigate the effects of LncRNA SNHG1 on the proliferation, migration, and epithelial-mesenchymal transition (EMT) of colorectal cancer cells (CRCs). Methods: 4 pairs of CRC tissue samples and their corresponding adjacent samples were analyzed by the human LncRNA microarray chip. The expression of LncSNHG1 in CRC cell lines was verified by qRT-PCR. Colony formation assays and CCK8 assays were applied to study the changes in cell proliferation. The transwell assay and wound healing experiments were used to verify the cell invasion and migration. EMT progression was confirmed finally. Results: LncSNHG1 was overexpressed both in CRC tissues and cell lines, while the miR-181b-5p expression was decreased in CRC cell lines. After knock-down of LncSNHG1, the proliferation, invasion, and migration of HT29 and SW620 cells were all decreased. Meanwhile, LncSNHG1 enhanced EMT progress through regulation of the miR-181b-5p/SMAD2 axis. Conclusion: LncSNHG1 promotes colorectal cancer cell proliferation and invasion through the miR-181b-5p/SMAD2 axis.

Identifiers

PMID35310912
PMCPMC8933095

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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.