Evidence map›Paper›PMID 27508021›Full record

ArticleAmerican journal of translational research2016

miR-448 suppresses proliferation and invasion by regulating IGF1R in colorectal cancer cells.

Bai Li, Liang Ge, Minghe Li, Lei Wang, Zhihong Li

RetractedOpen access · greenAbstract readRetracted Publication
In one paragraph

Article in American journal of translational research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Identification of Acute Myeloid Leukemia Bone Marrow Circulating MicroRNAs.International journal of molecular sciences · 2020
    Article
  6. Article
  7. Article
  8. Article
  9. miR-448 targets IDO1 and regulates CD8Journal for immunotherapy of cancer · 2019
    Article
  10. Article
  11. Article
  12. Lost in translation: The 3'-UTR ofEvolution, medicine, and public health · 2018
    Article
  13. Article
  14. Article
  15. microRNAs Make the Call in Cancer Personalized Medicine.Frontiers in cell and developmental biology · 2017
    Review
  16. Article
  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Bai LiDepartment of Colorectal and Anal Surgery, The First Hospital of Jilin University Changchun 130021, China.
Liang GeDepartment of Anesthesiology, The First Hospital of Jilin University Changchun 130021, China.
Minghe LiDepartment of Oral and Maxillofacial Surgery, School of Stomatology Hospital of Jilin University Changchun 130021, China.
Lei WangDepartment of Colorectal and Anal Surgery, The First Hospital of Jilin University Changchun 130021, China.
Zhihong LiDepartment of Thoracic Surgery, The First Hospital of Jilin University Changchun 130021, China.
Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulating evidence has demonstrated that miR-448 expression was downregulated, and exerted tumor suppressor roles in several types of cancer. However, the biological function and underlying mechanism of miR-448 in colorectal cancer (CRC) have not been elucidated. In this study, we detected the miR-448 expression in CRC tumor tissues and adjacent normal tissues (ANT) and five colorectal cancer cell lines by real time quantitative RT-PCR (qRT-PCR). Cell proliferation, colony formation, migration and invasion were investigated in CRC cells transfected miR-448 mimic or negative control mimic by MTT, colony forming, wound healing and transwell invasion assays, respectively. Target gene was identified by bioinformatic prediction, dual-luciferase reporter assay, qRT-PCR and Western blot. Our data proved that miR-448 expression was downregulated in CRC tissues and cell lines, and was inversely associated with advanced tumor-node-metastasis (TNM) stage (P < 0.01), and lymph node metastasis (P < 0.01). Overexpression of miR-448 suppressed CRC cell proliferation, colony formation, migration, and invasion. Moreover, we identified insulin-like growth factor 1 receptor (IGF1R) as a direct target gene of miR-448 in CRC cell. IGF1R expression was upregulated in CRC tissues and cell lines, and its expression was negatively correlated with the expression level of miR-448 in CRC tissues(r = -0.569, P = 0.002). In addition, IGF1R overexpression rescued the suppressive effect of miR-448-mediated CRC on cell proliferation, colony formation, migration and invasion. These results suggested that miR-448 might serve as a tumor suppressor in CRC partly through targeting IGF1R.

Indexed as

colorectal cancerIGF1RinvasionmiR-448proliferation

Identifiers

PMID27508021
PMCPMC4969437
OpenAlexW2520871085

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.