Evidence map›Paper›PMID 36505312›Full record

ArticleAmerican journal of translational research2022

miR-370 impacts the biological behavior of lung cancer cells by targeting the SMAD1 signaling pathway.

Zhaohui Tang, Yongjun Jiang, Sijuan Ding, Shaohui Jiang, Ruoting Tang, Pengfei Luo

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Observational
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

6 authors at 1 institution in 1 country.

Zhaohui TangDepartment of Oncology, The Central Hospital of Yongzhou No. 396 Yiyun Road, Yongzhou 425000, Hunan, China.
Yongjun JiangDepartment of Oncology, The Central Hospital of Yongzhou No. 396 Yiyun Road, Yongzhou 425000, Hunan, China.
Sijuan DingDepartment of Oncology, The Central Hospital of Yongzhou No. 396 Yiyun Road, Yongzhou 425000, Hunan, China.
Shaohui JiangDepartment of Oncology, The Central Hospital of Yongzhou No. 396 Yiyun Road, Yongzhou 425000, Hunan, China.
Ruoting TangDepartment of Oncology, The Central Hospital of Yongzhou No. 396 Yiyun Road, Yongzhou 425000, Hunan, China.
Pengfei LuoDepartment of Oncology, The Central Hospital of Yongzhou No. 396 Yiyun Road, Yongzhou 425000, Hunan, China.
Hunan University of Science and Engineering · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicroRNAs (miRNAs) have been identified to play a role in the development and progression of lung cancer (LC). As of now, the expression and function of miR-370 in LC are still under investigation. Accordingly, this study explores the role and mechanism of miR-370 in LC.

methodsMiR-370 mimics or inhibitors were used to transfect A549 and NCI-H460 cells to overexpress or inhibit miR-370. The colony formation test and Cell Counting Kit-8 were conducted to detect the cell proliferation activity, and transwell test and wound healing test were conducted to evaluate the cell invasion and migration activities. In addition, the downstream target genes of miR-370 in LC were verified by dual luciferase reporter assay and western blot.

resultsCompared to normal tissues and cell lineslines, the miR-370 expression in LC tissues and cells was decreased greatly. Compared to the negative control group, the up-regulation of miR-370 greatly intensified the apoptosis of NCI-H460 cells and weakened the migration, proliferation, and invasion of the cells. However, compared to the inhibitor-negative control group, the downregulation of miR-370 caused the opposite results. Additionally, SMAD family member 1 (SMAD1) was identified as a direct target of miR-370 in LC and could be inhibited by miR-370. Its overexpression restored the impact of miR-370 mimics on LC cells.

conclusionWith low expression in LC tissues and cell lineslines, miR-370 is a tumor suppressor that weakens the growth, invasion as well as migration of LC cells by inhibiting SMAD1 expression. Our results may provide novel insights for the biological treatment of LC.

Indexed as

lung cancerMiR-370SMAD1

Identifiers

PMID36505312
PMCPMC9730076
OpenAlexW4311282490

What OpenQuestion holds

Textmetadata
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.