Evidence map›Paper›PMID 31966507›Full record

ArticleInternational journal of clinical and experimental pathology2017

miR-138-5p acts as a tumor suppressor by targeting hTERT in human colorectal cancer.

Xiaotao Wang, Yongkui Zhao, Wenbin Cao, Changyou Wang, Bingfu Sun, Jianli Chen, Shuguang Li, Junmao Chen, Mingxin Cui, Bo Zhang and 4 more

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
0.4field-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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. miR-138-5p inhibits WiT-49 cell growth in vitro by downregulating TCF3 expression, and suppresses tumorigenesis in vivo.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  4. Article
  5. Article
  6. The functional role of circular RNAs in the pathogenesis of retinoblastoma: a new potential biomarker and therapeutic target?Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. TERT-Regulation and Roles in Cancer Formation.Frontiers in immunology · 2020
    Review
  17. miRNAs-Based Molecular Signature forJournal of immunology research · 2020
    Article
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

14 authors at 1 institution in 1 country.

Xiaotao WangDepartment of General Surgery, Affiliated Hospital of North China University of Science and Technology Tangshan 063000, Hebei, China.
Yongkui ZhaoDepartment of General Surgery, Affiliated Hospital of North China University of Science and Technology Tangshan 063000, Hebei, China.
Wenbin CaoDepartment of General Surgery, Affiliated Hospital of North China University of Science and Technology Tangshan 063000, Hebei, China.
Changyou WangDepartment of General Surgery, Affiliated Hospital of North China University of Science and Technology Tangshan 063000, Hebei, China.
Bingfu SunDepartment of General Surgery, Affiliated Hospital of North China University of Science and Technology Tangshan 063000, Hebei, China.
Jianli ChenDepartment of General Surgery, Affiliated Hospital of North China University of Science and Technology Tangshan 063000, Hebei, China.
Shuguang LiDepartment of General Surgery, Affiliated Hospital of North China University of Science and Technology Tangshan 063000, Hebei, China.
Junmao ChenDepartment of General Surgery, Affiliated Hospital of North China University of Science and Technology Tangshan 063000, Hebei, China.
Mingxin CuiDepartment of General Surgery, Affiliated Hospital of North China University of Science and Technology Tangshan 063000, Hebei, China.
Bo ZhangDepartment of General Surgery, Affiliated Hospital of North China University of Science and Technology Tangshan 063000, Hebei, China.
Guanghua YangDepartment of General Surgery, Affiliated Hospital of North China University of Science and Technology Tangshan 063000, Hebei, China.
Yang LiuDepartment of General Surgery, Affiliated Hospital of North China University of Science and Technology Tangshan 063000, Hebei, China.
Xiangyang YuDepartment of General Surgery, Affiliated Hospital of North China University of Science and Technology Tangshan 063000, Hebei, China.
Guozhi ZhangDepartment of General Surgery, Affiliated Hospital of North China University of Science and Technology Tangshan 063000, Hebei, China.
North China University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is the second most common cancer in the world. The incidence of this cancer is increasing in the developing countries. Mechanism of CRC tumorigenesis has been widely studied at the molecular levels, and has been recently proposed microRNAs as novel players in CRC. It has been reported that microRNA-138-5p (miR-138-5p) play key roles in different kinds of human cancers. However, the roles and underlying molecular mechanisms of miR-138-5p in CRC have not been adequately elucidated. Thus, the aim of the present study was to investigate the roles and possible regulatory mechanisms of miR-138-5p in CRC. In this study, we demonstrated that miR-138-5p was significantly down-regulated in CRC tissue samples and cell lines. Functional analyses indicated that the overexpression of miR-138-5p significantly delayed cell proliferation, reduced colony formation and increased apoptosis in CRC cell lines. Moreover, human telomerase reverse transcriptase (hTERT), an important oncogene in the management of tumors, was confirmed as a direct target of miR-138-5p in CRC cells. We also found that the hTERT expression was increased in CRC tissues and was inversely correlated with miR-138-5p. Further study showed that the restoration of hTERT expression by an overexpressing plasmid could reverse the effects of miR-138-5p on proliferation and apoptosis of CRC cells. Taken together, these data defines a major suppresses proliferation and promotes apoptosis role for miR-138-5p, a microRNA functions as a tumor suppressor in CRC, by directly targeting hTERT, which would be provide a new strategy for future CRC therapies.

Indexed as

apoptosisCRChTERTMicroRNA-138-5pproliferation

Identifiers

PMID31966507
PMCPMC6966048
OpenAlexW3027374960

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.